C. Bodemer

发表

The NF-kappaB signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes.

A. Smahi, G. Courtois, S. Rabia, 2002, Human molecular genetics.

The EDAR370A allele attenuates the severity of hypohidrotic ectodermal dysplasia caused by EDA gene mutation

A. Smahi, C. Bodemer, A. Munnich, 2012, The British journal of dermatology.

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

Yang Liu, Sen Yang, Miao Sun, 2009, Nature Genetics.

Detection of interferon alpha protein reveals differential levels and cellular sources in disease

F. Rieux-Laucat, C. Bodemer, Y. Crow, 2017, The Journal of experimental medicine.

Pediatric mastocytosis is a clonal disease associated with D816V and other activating c-KIT mutations.

L. Thomas, C. Bodemer, J. Launay, 2010, The Journal of investigative dermatology.

Human lipodystrophies linked to mutations in A-type lamins and to HIV protease inhibitor therapy are both associated with prelamin A accumulation, oxidative stress and premature cellular senescence

C. Bodemer, B. Donadille, C. Vigouroux, 2007, Cell Death and Differentiation.

Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases

A. Smahi, C. Bodemer, A. Munnich, 2011, Human mutation.

LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome.

C. Bodemer, D. Hohl, A. Hovnanian, 2003, Human molecular genetics.

Unusual presentation of a severe autosomal recessive anhydrotic ectodermal dysplasia with a novel mutation in the EDAR gene

A. Smahi, C. Bodemer, A. Mégarbané, 2008, American journal of medical genetics. Part A.

Aplasia cutis congenita with dystrophic epidermolysis bullosa: clinical and mutational study

C. Bodemer, M. del Río, C. Chiaverini, 2014, The British journal of dermatology.

Assessment of Type I Interferon Signaling in Pediatric Inflammatory Disease

C. Bodemer, Y. Crow, Naoki Kitabayashi, 2016, Journal of Clinical Immunology.

Secukinumab demonstrates high efficacy and a favourable safety profile in paediatric patients with severe chronic plaque psoriasis: 52‐week results from a Phase 3 double‐blind randomized, controlled trial

C. Bodemer, K. Kingo, A. Kaszuba, 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.

Topical Corticosteroid Concerns Among Parents of Children with Psoriasis versus Atopic Dermatitis: A French Multicenter Cross-Sectional Study

C. Bodemer, C. Chiaverini, S. Barbarot, 2018, American Journal of Clinical Dermatology.

Efficacy of colchicine in a child with relapsing bullous Henoch-Schönlein purpura

C. Bodemer, M. Chalumeau, B. Terrier, 2015, European Journal of Pediatrics.

Treatments and outcomes in juvenile linear scleroderma: a narrative systematic review

C. Bodemer, A. Maruani, M. Samimi, 2018, European Journal of Dermatology.

Alterations of the IKBKG locus and diseases: an update and a report of 13 novel mutations

M. D'urso, A. Smahi, S. Rabia, 2008, Human mutation.

Skin manifestations of COVID‐19 in children: Part 2

R. Grimalt, C. Bodemer, V. Kinsler, 2020, Clinical and experimental dermatology.

C. Bodemer, S. Hadj-Rabia, S. Doan, 2019, Experimental dermatology.

Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009.

C. Bodemer, M. Akiyama, H. Shimizu, 2010, Journal of the American Academy of Dermatology.

Peripheral microchimerism in long-term cadaveric-kidney allograft recipients

C. Bodemer, C. Legendre, J. Bach, 1994, The Lancet.

Skin markers of occult spinal dysraphism in children: a review of 54 cases.

C. Bodemer, F. Brunelle, S. Hadj-Rabia, 2004, Archives of dermatology.

Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I

A. Fischer, R. Döffinger, C. Bodemer, 2010, The Journal of experimental medicine.

Chronic Mucocutaneous Candidiasis in Humans with Inborn Errors of Interleukin-17 Immunity

C. Bodemer, J. Casanova, C. Picard, 2011, Science.

Stability and Formulation of Erlotinib in Skin Creams

C. Bodemer, P. Secrétan, J. Schlatter, 2022, Molecules.

Efficacy and safety of thalidomide in patients with inflammatory manifestations of chronic granulomatous disease: a retrospective case series.

A. Fischer, C. Bodemer, H. Sokol, 2013, The Journal of allergy and clinical immunology.

Long-term efficacy of the interleukin-1 receptor antagonist anakinra in ten patients with neonatal-onset multisystem inflammatory disease/chronic infantile neurologic, cutaneous, articular syndrome.

C. Bodemer, N. Boddaert, G. Pinto, 2010, Arthritis and rheumatism.

Challenges in Treating Genodermatoses: New Therapies at the Horizon

C. Bodemer, D. Hohl, F. Giuliano, 2022, Frontiers in Pharmacology.

Combination of palmoplantar keratoderma and hair shaft anomalies, the warning signal of severe arrhythmogenic cardiomyopathy: a systematic review on genetic desmosomal diseases

C. Bodemer, S. Hadj-Rabia, L. Polivka, 2015, Journal of Medical Genetics.

Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study

A. Vanderver, C. Bodemer, B. Gener, 2013, The Lancet Neurology.

Keratitis–ichthyosis–deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patients

C. Bodemer, C. Prins, J. Saurat, 2007, The British journal of dermatology.

Germline mosaicism in keratitis–ichthyosis–deafness syndrome: pre‐natal diagnosis in a familial lethal form

C. Bodemer, E. Sbidian, S. Hadj-Rabia, 2010, Clinical genetics.

A familial T‐cell lymphoma with γδ phenotype and an original location: Possible role of chronic Epstein–Barr virus infection

S. Schraub, C. Bodemer, F. Sigaux, 1996 .

Corneodesmosomal cadherins are preferential targets of stratum corneum trypsin- and chymotrypsin-like hyperactivity in Netherton syndrome.

C. Bodemer, A. Ishida-Yamamoto, A. Hovnanian, 2006, The Journal of investigative dermatology.

Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome

C. Bodemer, Y. Barrandon, A. Hovnanian, 2000, Nature Genetics.

Corrigendum: Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

S. Cichon, M. Nöthen, C. Bodemer, 2009, Nature Genetics.

Treatment of Painful Palmoplantar Keratoderma Related to Pachyonychia Congenita Using EGFR Inhibitors

C. Bodemer, C. Boucheix, J. Schlatter, 2022, Biomedicines.

Importance of therapeutic patient education in ichthyosis: results of a prospective single reference center study

C. Bodemer, S. Hadj-Rabia, C. Taïeb, 2013, Orphanet Journal of Rare Diseases.

Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus

A. Smahi, G. Courtois, C. Bodemer, 2007, Human mutation.

Emergency management in epidermolysis bullosa: consensus clinical recommendations from the European reference network for rare skin diseases

C. Bodemer, C. Sălăvăstru, N. Bellon, 2020, Orphanet Journal of Rare Diseases.

Subcutaneous Panniculitis-like T-cell Lymphoma: Immunosuppressive Drugs Induce Better Response than Polychemotherapy.

C. Bodemer, T. Petrella, N. Brousse, 2017, Acta dermato-venereologica.

Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis

C. Bodemer, Y. Barrandon, A. Hovnanian, 2000, European Journal of Human Genetics.

Enhanced cGAS-STING-dependent interferon signaling associated with mutations in ATAD3A

C. Bodemer, C. Wouters, Y. Crow, 2021, bioRxiv.

Enhanced cGAS-STING–dependent interferon signaling associated with mutations in ATAD3A

C. Bodemer, C. Wouters, Y. Crow, 2021, The Journal of experimental medicine.

An Asymptomatic Subcutaneous Nodule of the Lower Back: A Sentinel Lesion for a Diagnosis Not to Be Missed: Answer

C. Bodemer, Y. de Prost, S. Fraitag, 2013, The American Journal of dermatopathology.

Cutaneous EBV-related lymphoproliferative disorder in a 15-year-old boy with AIDS: an unusual clinical presentation.

C. Bodemer, N. Brousse, S. Blanche, 2002, Journal of pediatric hematology/oncology.

Statistical evaluation of diagnostic and prognostic features of CD30+ cutaneous lymphoproliferative disorders: a clinicopathologic study of 65 cases.

C. Bodemer, K. Pulford, J. Bosq, 1998, The American journal of surgical pathology.

Cutaneous B-cell lymphoblastic lymphoma in children: a rare diagnosis.

C. Bodemer, N. Brousse, O. Boccara, 2012, Journal of the American Academy of Dermatology.

JAK inhibitors are effective in a subset of patients with juvenile dermatomyositis: a monocentric retrospective study.

C. Bodemer, D. Duffy, J. Herbeuval, 2021, Rheumatology.

Differential Expression of Interferon-Alpha Protein Provides Clues to Tissue Specificity Across Type I Interferonopathies

C. Bodemer, Y. Crow, S. Orcesi, 2021, Journal of Clinical Immunology.

Heterozygous RELA mutations cause early-onset systemic lupus erythematosus by hijacking the NF-κB pathway towards transcriptional activation of type-I Interferon genes

F. Rieux-Laucat, C. Bodemer, C. Picard, 2020, bioRxiv.

Circulating Interferon‐α Measured With a Highly Sensitive Assay as a Biomarker for Juvenile Inflammatory Myositis Activity: Comment on the Article by Mathian et al

C. Bodemer, Y. Crow, D. Duffy, 2020, Arthritis & rheumatology.

Anti-MDA5 juvenile idiopathic inflammatory myopathy: a specific subgroup defined by differentially enhanced interferon-α signalling.

C. Bodemer, Y. Crow, Naoki Kitabayashi, 2019, Rheumatology.

Inhibition of IFNα secretion in cells from patients with juvenile dermatomyositis under TBK1 inhibitor treatment revealed by single-molecular assay technology.

C. Bodemer, Y. Crow, D. Duffy, 2019, Rheumatology.

A child with severe juvenile dermatomyositis treated with ruxolitinib

C. Bodemer, Y. Crow, D. Duffy, 2018 .

A child with severe juvenile dermatomyositis treated with ruxolitinib.

C. Bodemer, Y. Crow, D. Duffy, 2018, Brain : a journal of neurology.

Mechanism of Oleogel‐S10: A triterpene preparation for the treatment of epidermolysis bullosa

C. Bodemer, H. Ott, D. Kiritsi, 2019, Dermatologic therapy.

Successful Allogeneic Hemopoietic Stem Cell Transplantation in a Child Who Had Anhidrotic Ectodermal Dysplasia With Immunodeficiency

A. Fischer, C. Bodemer, J. Casanova, 2006, Pediatrics.

A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency.

A. Fischer, A. Smahi, G. Courtois, 2003, The Journal of clinical investigation.

Syndrome hyperéosinophilique: aspects cliniques

C. Bodemer, O. Blétry, P. Godeau, 1987 .

Oral epigallocatechin-3-gallate for treatment of dystrophic epidermolysis bullosa: a multicentre, randomized, crossover, double-blind, placebo-controlled clinical trial

C. Bodemer, C. Chiaverini, Pierre Vabres, 2016, Orphanet Journal of Rare Diseases.

NEMO Mutations in 2 Unrelated Boys With Severe Infections and Conical Teeth

C. Bodemer, J. Casanova, C. Picard, 2005, Pediatrics.

Clonal Cytophagic Histiocytic Panniculitis in Children May Be Cured by Cyclosporine A

C. Bodemer, C. Wouters, B. Bader-Meunier, 2013, Pediatrics.

Three Novel Point Mutations in the Keratinocyte Transglutaminase (TGK) Gene in Lamellar Ichthyosis: Significance for Mutant Transcript Level, TGK Immunodetection and Activity

C. Bodemer, M. Lathrop, Y. Barrandon, 1997, European journal of human genetics : EJHG.

Identification of new RECQL4 mutations in Caucasian Rothmund-Thomson patients and analysis of sensitivity to a wide range of genotoxic agents.

C. Bodemer, S. Queillé, A. Sarasin, 2008, Mutation research.

Cutaneous manifestations of immune dysregulation, polyendocrinopathy, enteropathy, X‐linked (IPEX) syndrome

F. Rieux-Laucat, C. Bodemer, N. Brousse, 2009, The British journal of dermatology.

Verrucous hemangioma (also known as verrucous venous malformation): A vascular anomaly frequently misdiagnosed as a lymphatic malformation

C. Bodemer, F. Brunelle, S. Hadj-Rabia, 2018, Pediatric dermatology.

Skin manifestations of COVID‐19 in children: Part 1

R. Grimalt, C. Bodemer, V. Kinsler, 2020, Clinical and experimental dermatology.

CEMARA: a Web Dynamic Application Within a N-tier Architecture for Rare Diseases

Mohamed Ben Saïd, Paul Landais, Jean Philippe Jaïs, 2008, MIE.

Epidermolysis bullosa in France: management in the National Reference Center for Genodermatosis.

C. Bodemer, 2010, Dermatologic clinics.

Acro‐osteolysis, keloid like‐lesions, distinctive facial features, and overgrowth: Two newly recognized patients with premature aging syndrome, penttinen type

C. Bodemer, S. Hadj-Rabia, V. Cormier-Daire, 2013, American journal of medical genetics. Part A.

Olmsted syndrome with erythromelalgia caused by recessive transient receptor potential vanilloid 3 mutations

C. Bodemer, S. Duchatelet, P. Nitschké, 2014, The British journal of dermatology.

Late recurrence of inflammatory first-stage lesions in incontinentia pigmenti: an unusual phenomenon and a fascinating pathologic mechanism.

C. Bodemer, S. Hadj-Rabia, Y. de Prost, 2003, Archives of dermatology.

Skin elastic fibers in Williams syndrome.

C. Bodemer, S. Lyonnet, Pierre Vabres, 1999, American journal of medical genetics.

P.197 Myogenic progenitor cells exhibit IFN type I-driven pro-angiogenic properties and molecular signature during juvenile dermatomyositis

C. Bodemer, J. Chelly, M. Rodero, 2017, Neuromuscular Disorders.

Safety and Efficacy of Rituximab in Severe Juvenile Dermatomyositis: Results from 9 Patients from the French Autoimmunity and Rituximab Registry

C. Bodemer, J. Gottenberg, J. Sibilia, 2011, The Journal of Rheumatology.

Severe Abdominal Manifestations in Juvenile Dermatomyositis.

C. Bodemer, B. Bader-Meunier, P. Quartier, 2019, Journal of pediatric gastroenterology and nutrition.

Muscle ischaemia associated with NXP2 autoantibodies: a severe subtype of juvenile dermatomyositis

C. Bodemer, G. Bassez, B. Bader-Meunier, 2018, Rheumatology.

C. Bodemer, B. Bader-Meunier, C. Barnérias, 2015, Rheumatology.

Thrombotic Microangiopathy and Purtscher-like Retinopathy as a Rare Presentation of Juvenile Dermatomyositis

C. Bodemer, N. Costedoat-Chalumeau, B. Bader-Meunier, 2012, Pediatrics.

Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formation.

C. Bodemer, M. Lathrop, Y. Barrandon, 1997, American journal of human genetics.

Severe cardiac involvement in children with systemic sclerosis and myositis.

C. Bodemer, A. Prieur, P. Acar, 2002, The Journal of rheumatology.

Rubella Virus-Associated Cutaneous Granulomatous Disease: a Unique Complication in Immune-Deficient Patients, Not Limited to DNA Repair Disorders

C. Bodemer, C. Klein, H. Ochs, 2019, Journal of Clinical Immunology.

Presentations and outcomes of juvenile dermatomyositis patients admitted to intensive care units.

C. Bodemer, R. Salomon, B. Bader-Meunier, 2017, Rheumatology.

Panniculitis in Children

C. Bodemer, 2019, Harper's Textbook of Pediatric Dermatology.

The challenging management of a series of 43 infants with Netherton syndrome: unexpected complications and novel mutations *

C. Bodemer, A. Hovnanian, A. Lapillonne, 2020, The British journal of dermatology.

Prenatal diagnosis of a lethal form of Netherton syndrome by SPINK5 mutation analysis

C. Bodemer, C. Stoll, P. Calvas, 2002, Prenatal diagnosis.

Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 families.

C. Bodemer, A. Hovnanian, A. Irvine, 2002, The Journal of investigative dermatology.

C. Bodemer, Elif Yilmaz Gulec, A. Gezdirici, 2018, Experimental dermatology.

Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility

C. Bodemer, J. Uitto, J. McGrath, 2020, The British journal of dermatology.

Immunohistochemical detection of granulocyte/macrophage colony‐stimulating factor in Langerhans' cell histiocytosis

C. Bodemer, N. Brousse, M. Peuchmaur, 1993, Histopathology.

Severe Skin Complications After Small Bowel Transplantation: Graft-Versus-Host Disease, DRESS, Virus, or Drug Toxicity?

C. Bodemer, P. Frange, O. Goulet, 2016, Transplantation.

Paediatric Mastocytosis

C. Bodemer, L. Polivka, 2019, Harper's Textbook of Pediatric Dermatology.

Feline maculopapular cutaneous mastocytosis: a retrospective study of 13 cases and proposal for a new classification

C. Bodemer, J. Fontaine, M. Heimann, 2018, Journal of feline medicine and surgery.

Paediatric mastocytosis: long‐term follow‐up of 53 patients with whole sequencing of KIT. A prospective study

C. Bodemer, J. Jais, P. Dubreuil, 2018, The British journal of dermatology.

Topical pimecrolimus for paediatric cutaneous mastocytosis

C. Bodemer, E. Sprecher, S. Hadj-Rabia, 2018, Clinical and experimental dermatology.

Kaposiform Haemangioendothelioma-spectrum Lesions with Kasabach-Merritt Phenomenon: Retrospective Analysis and Long-term Outcome.

C. Bodemer, F. Brunelle, D. Orbach, 2016, Acta dermato-venereologica.

Proposal for a 6‐step approach for differential diagnosis of neonatal erythroderma

C. Bodemer, M. van Gijn, V. Sigurdsson, 2022, Journal of the European Academy of Dermatology and Venereology : JEADV.

Three severe cases of EBS Dowling-Meara caused by missense and frameshift mutations in the keratin 14 gene.

C. Bodemer, A. Hovnanian, S. Hadj-Rabia, 2006, The Journal of investigative dermatology.

Epigallocatechin gallate's protective effect against MMP7 in recessive dystrophic epidermolysis bullosa patients.

C. Bodemer, G. Godeau, F. Fioretti, 2007, The Journal of investigative dermatology.

Staphylococcal necrotizing fasciitis in the mammary region in childhood: a report of five cases.

C. Bodemer, Y. de Prost, M. Cloup, 1997, The Journal of pediatrics.

Prognostic factors in primary cutaneous lymphomas other than mycosis fungoides and the Sézary syndrome. The French Study Group on Cutaneous Lymphomas.

C. Bodemer, G. Hédelin, L. Vaillant, 1999, Blood.

Neonatal and early infantile cutaneous langerhans cell histiocytosis: comparison of self-regressive and non-self-regressive forms.

C. Bodemer, N. Brousse, M. Battistella, 2010, Archives of Dermatology.

[Current concepts and treatment advances in systemic mastocytosis].

C. Bodemer, P. Dubreuil, O. Hermine, 2009, La Revue de medecine interne.

Hypophosphatemic rickets: A rare complication of congenital melanocytic nevus syndrome

C. Bodemer, G. Pinto, S. Hadj-Rabia, 2020, Pediatric dermatology.

Cutaneous involvement in patients with angioimmunoblastic lymphadenopathy with dysproteinemia: a clinical, immunohistological, and molecular analysis.

C. Bodemer, P. Courville, L. Laroche, 2000, Archives of dermatology.

Interferon-β Therapy in a Patient with Incontinentia Pigmenti and Autoantibodies against Type I IFNs Infected with SARS-CoV-2

C. Bodemer, J. Casanova, P. Bastard, 2021, Journal of Clinical Immunology.

Successful management of severe infant bullous pemphigoid with omalizumab

C. Bodemer, P. Reix, F. Cambazard, 2012, The British journal of dermatology.

Clinical and Therapeutic Aspects of Linear Psoriasis: A Study of 30 Cases

C. Bodemer, C. Chiaverini, M. Richard, 2018, American Journal of Clinical Dermatology.

Nail Psoriasis: A Systematic Evaluation in 313 Children with Psoriasis

C. Bodemer, S. Hadj-Rabia, F. Boralevi, 2017 .

Microchimerism frequency two to thirty years after cadaveric kidney transplantation.

C. Bodemer, C. Legendre, J. Bach, 1994, Human immunology.

A new TRPV3 missense mutation in a patient with Olmsted syndrome and erythromelalgia.

C. Bodemer, S. Duchatelet, C. Bole-Feysot, 2014, JAMA dermatology.

Novel mutation in GJB4 gene (connexin 30.3) in a family with erythrokeratodermia variabilis.

C. Bodemer, E. Sbidian, S. Hadj-Rabia, 2013, Acta dermato-venereologica.

Mutation in MMP2 gene may result in scleroderma-like skin thickening

C. Bodemer, B. Bader-Meunier, L. Bonafė, 2015, Annals of the rheumatic diseases.

Angioedema in Renal Transplant Recipients on Sirolimus

C. Bodemer, E. Morelon, Y. de Prost, 2007, Dermatology.

Devastating gynecological infections in women with STAT3 deficiency.

C. Bodemer, N. Mahlaoui, O. Lortholary, 2020, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Acne in recipients of renal transplantation treated with sirolimus: clinical, microbiologic, histologic, therapeutic, and pathogenic aspects.

C. Bodemer, E. Morelon, Y. de Prost, 2006, Journal of the American Academy of Dermatology.

Efficacy and Tolerance of Sirolimus (Rapamycin) for Extracranial Arteriovenous Malformations in Children and Adults.

C. Bodemer, O. Boccara, D. Herbreteau, 2019, Acta dermato-venereologica.

Lymphomatoid papulosis in children: a series of 25 cases

C. Bodemer, N. Brousse, Y. Prost, 2014, The British journal of dermatology.

Efficacy of intravenous immunoglobulins in sclerodermatomyositis

C. Bodemer, Y. Prost, B. Wechsler, 1990, The British journal of dermatology.

Skin manifestations of COVID‐19 in children: Part 3

R. Grimalt, C. Bodemer, V. Kinsler, 2020, Clinical and experimental dermatology.

Severe cutaneous bacillus Calmette–Guérin infection in immunocompromised children: the relevance of skin biopsy

A. Fischer, C. Bodemer, C. Picard, 2013, Journal of cutaneous pathology.

[Soft tissue tumors in neonates].

C. Bodemer, D. Orbach, O. Oberlin, 2009, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Immune reactivity to type VII collagen: implications for gene therapy of recessive dystrophic epidermolysis bullosa

C. Bodemer, A. Hovnanian, Z. Vitezica, 2010, Gene Therapy.

Multicentre consensus recommendations for skin care in inherited epidermolysis bullosa

C. Bodemer, S. Hadj-Rabia, Guglielmo Salvatori, 2014, Orphanet Journal of Rare Diseases.

Incontinentia pigmenti and hypomelanosis of Ito.

C. Bodemer, 2013, Handbook of clinical neurology.

Randomised double-blind placebo-controlled trial of local cyclosporin in atopic dermatitis.

C. Bodemer, Y. de Prost, D. Teillac, 1989, Acta dermato-venereologica. Supplementum.

[Cutaneous manifestations disclosing T-cell gamma/delta lymphoma in a 13-year-old-girl].

C. Bodemer, P. Agache, C. Griscelli, 1993, Annales de dermatologie et de venereologie.

Role of cytotoxic T cells in chronic alopecia areata.

C. Bodemer, N. Brousse, L. Chatenoud, 2000, The Journal of investigative dermatology.

A toxic palmitoylation of Cdc42 enhances NF-κB signaling and drives a severe autoinflammatory syndrome.

T. Molina, A. Smahi, C. Bodemer, 2020, The Journal of allergy and clinical immunology.

Nutritional outcome in children with severe generalized recessive dystrophic epidermolysis bullosa: a short‐ and long‐term evaluation of gastrostomy and enteral feeding

C. Bodemer, Y. de Prost, V. Colomb, 2012, The British journal of dermatology.

Self‐healing juvenile cutaneous mucinosis: Clinical and histopathologic findings of 9 patients: The relevance of long‐term follow‐up

C. Bodemer, B. Bader-Meunier, I. Melki, 2017, Journal of the American Academy of Dermatology.

Epidermolysis bullosa acquisita in childhood.

C. Bodemer, Y. de Prost, I. Bourgault-Villada, 1997, Archives of dermatology.

Beard infantile hemangioma and subglottic involvement: are median pattern and telangiectatic aspect the clue?

C. Bodemer, S. Hadj-Rabia, O. Boccara, 2016, Journal of the European Academy of Dermatology and Venereology : JEADV.

Management of congenital ichthyoses: European guidelines of care, part one

C. Bodemer, D. Hohl, A. Pietrzak, 2018, The British journal of dermatology.

Reduced Expression of the Epithelial Adhesion Ligand Laminin 5 in the Skin Causes Intradermal Tissue Separation*

C. Bodemer, J. Ortonne, L. Pulkkinen, 2001, The Journal of Biological Chemistry.

Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response

Jonathan C. Fuller, D. Bonthron, E. Bertini, 2009, Nature Genetics.

Folliculocystic and collagen hamartoma of tuberous sclerosis complex.

C. Bodemer, R. Happle, V. Sybert, 2012, Journal of the American Academy of Dermatology.

Efficacy and tolerability of the investigational topical cream SD-101 (6% allantoin) in patients with epidermolysis bullosa: a phase 3, randomized, double-blind, vehicle-controlled trial (ESSENCE study)

C. Bodemer, A. Paller, D. Murrell, 2020, Orphanet Journal of Rare Diseases.

Onychomycosis in children

C. Bodemer, Y. Prost, C. Hennequin, 1996 .

Neonatal and infantile erythrodermas: a retrospective study of 51 patients.

C. Bodemer, Y. de Prost, S. Fraitag, 2000, Archives of dermatology.

Neonatal and Infantile Erythrodermas

C. Bodemer, Y. Prost, S. Fraitag, 2000 .

Cyclosporine in childhood psoriasis.

C. Bodemer, Y. de Prost, E. Mahé, 2001, Archives of dermatology.

Granulomatous inflammation in cartilage-hair hypoplasia: risks and benefits of anti-TNF-α mAbs.

A. Fischer, C. Bodemer, C. Wouters, 2011, The Journal of allergy and clinical immunology.

Phacomatosis pigmentokeratotica with nephroblastoma and juvenile hypertension.

C. Bodemer, R. Happle, R. Salomon, 2010, Acta dermato-venereologica.

Cutaneous granulomas with primary immunodeficiency in children: a report of 17 new patients and a review of the literature

C. Bodemer, N. Mahlaoui, B. Neven, 2019, Journal of the European Academy of Dermatology and Venereology : JEADV.

Malassezia folliculitis in an infant.

C. Bodemer, M. Kharfi, S. Anane, 2013, Medical mycology case reports.

Neonatal Behçet's disease.

C. Bodemer, P. Buisson, O. Fain, 1995, The American journal of medicine.

Hair and skin disorders as signs of mitochondrial disease.

C. Bodemer, A. Munnich, P. Rustin, 1999, Pediatrics.

Cutaneous manifestations of methylmalonic and propionic acidaemia: a description based on 38 cases

C. Bodemer, Y. Prost, J. Saudubray, 1994, The British journal of dermatology.

Main Life-Threatening Dermatoses in Neonatal Period and in Infancy

C. Bodemer, 2009 .

[Impact of sex and age on the clinical and epidemiological aspects of childhood psoriasis: Data from a French cross-sectional multicentre study].

C. Bodemer, C. Chiaverini, S. Barbarot, 2016, Annales de dermatologie et de venereologie.

Outcomes of Systemic Treatment in Children and Adults With Netherton Syndrome: A Systematic Review

C. Bodemer, S. Pasmans, A. Ragamin, 2022, Frontiers in Immunology.

Early skin biopsy is helpful for the diagnosis and management of neonatal and infantile erythrodermas

C. Bodemer, N. Brousse, A. Hovnanian, 2010, Journal of cutaneous pathology.

The histopathology of congenital haemangioma and its clinical correlations: a long‐term follow‐up study of 55 cases

C. Bodemer, O. Boccara, A. Coulomb, 2020, Histopathology.

Pityriasis Lichenoides: A Large Histopathological Case Series With a Focus on Adnexotropism.

T. Molina, C. Bodemer, S. Fraitag, 2020, The American Journal of dermatopathology.

A familial case of Keratitis-Ichthyosis-Deafness (KID) syndrome with the GJB2 mutation G45E.

C. Bodemer, F. Denoyelle, S. Hadj-Rabia, 2008, European journal of medical genetics.

Management of congenital ichthyoses: European guidelines of care, part two

C. Bodemer, D. Hohl, F. Poot, 2018, The British journal of dermatology.

High frequency of detection of human papillomaviruses associated with epidermodysplasia verruciformis in children with psoriasis

C. Bodemer, Y. Prost, M. Favre, 2003, The British journal of dermatology.

Double-blind randomized placebo-controlled trial of local cyclosporine in atopic dermatitis.

C. Bodemer, Y. de Prost, D. Teillac, 1989, Archives of dermatology.

Cutaneous findings in sporadic and familial autosomal dominant hyper-IgE syndrome: a retrospective, single-center study of 21 patients diagnosed using molecular analysis.

A. Fischer, C. Bodemer, C. Picard, 2011, Journal of the American Academy of Dermatology.

Unilateral laterothoracic exanthem in children: a new disease?

C. Bodemer, Y. de Prost, 1992, Journal of the American Academy of Dermatology.

[Cutaneous granulomatous lesions in congenital immune deficiencies. 5 cases].

C. Bodemer, C. Paul, Y. de Prost, 1995, Annales de dermatologie et de venereologie.

Subcutaneous fat necrosis of the newborn: a systematic evaluation of risk factors, clinical manifestations, complications and outcome of 16 children

C. Bodemer, S. Hadj-Rabia, Y. Prost, 2007, The British journal of dermatology.

Cutaneous and Visceral Chronic Granulomatous Disease Triggered by a Rubella Virus Vaccine Strain in Children With Primary Immunodeficiencies

T. Molina, C. Bodemer, B. le Bail, 2017, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Live rubella virus vaccine long-term persistence as an antigenic trigger of cutaneous granulomas in patients with primary immunodeficiency.

C. Bodemer, N. Mahlaoui, M. Eloit, 2014, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.

Congenital Erosive and Vesicular Dermatosis: A New Case and Review of the Literature

C. Bodemer, S. Hadj-Rabia, D. Wallach, 2012, Pediatric dermatology.

Epidermal necrolysis French national diagnosis and care protocol (PNDS; protocole national de diagnostic et de soins)

C. Bodemer, O. Dereure, O. Chosidow, 2018, Orphanet Journal of Rare Diseases.

Association of acute neutrophilic dermatosis and myelodysplastic syndrome with (6; 9) chromosome translocation: a case report and review of the literature

C. Bodemer, B. Mégarbane, I. Radford‐Weiss, 2000, The British journal of dermatology.

Familial benign chronic pemphigus and doxycycline: a review of 6 cases

C. Bodemer, S. Fraitag, L. Le Saché‐de Peufeilhoux, 2014, Journal of the European Academy of Dermatology and Venereology : JEADV.

Reduction in pain following treatment with ranolazine in primary erythromelalgia: a case report

C. Bodemer, C. Greco, M. Viallard, 2018, The British journal of dermatology.

[Generalized exanthematous pustular dermatophytid, a rare clinical presentation of dermatophytid reaction].

C. Bodemer, S. Hadj-Rabia, O. Boccara, 2014, Annales de dermatologie et de venereologie.

Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis

A. Fischer, C. Bodemer, J. Casanova, 2011, The Journal of experimental medicine.

Efficacy and tolerability of methotrexate in severe childhood alopecia areata

C. Bodemer, S. Barbarot, Pierre Vabres, 2011, The British journal of dermatology.

Autosomal Dominant STAT3 Deficiency and Hyper-IgE Syndrome: Molecular, Cellular, and Clinical Features From a French National Survey

A. Fischer, C. Bodemer, J. Casanova, 2012, Medicine.

Treatment of hereditary palmoplantar keratoderma: a review by analysis of the literature *

C. Bodemer, J. Mazereeuw-Hautier, E. O’Toole, 2020, The British journal of dermatology.

Unique subungueal keratoacanthoma revealing incontinentia pigmenti

A. Smahi, C. Bodemer, O. Chosidow, 2016, Journal of the European Academy of Dermatology and Venereology : JEADV.

Long‐term evolving profile of childhood autoimmune blistering diseases: Retrospective study on 38 children

C. Bodemer, S. Hadj-Rabia, O. Boccara, 2019, Journal of the European Academy of Dermatology and Venereology : JEADV.

[Sirolimus-induced onychopathy in renal transplant recipients].

C. Bodemer, E. Morelon, Y. de Prost, 2006, Annales de dermatologie et de venereologie.

Presence of chimeric maternally derived keratinocytes in cutaneous inflammatory diseases of children: the example of pityriasis lichenoides.

C. Bodemer, K. Khosrotehrani, M. Oster, 2006, The Journal of investigative dermatology.

Improvement of epidermal covering on AEC patients with severe skin erosions by PRIMA-1MET/APR-246

C. Bodemer, C. Missero, E. Aberdam, 2020, Cell Death & Disease.

Pityriasis lichenoides of childhood with atypical CD30-positive cells and clonal T-cell receptor gene rearrangements.

C. Bodemer, C. Paul, Y. de Prost, 1996, Journal of the American Academy of Dermatology.

Cutaneous hematologic disorders in children

C. Bodemer, N. Brousse, O. Boccara, 2012, Pediatric blood & cancer.

Pediatric patients with cutaneous melanoma: A European study

C. Bodemer, C. Garbe, A. Ferrari, 2018, Pediatric blood & cancer.

A frequent functional SNP in the MMP1 promoter is associated with higher disease severity in recessive dystrophic epidermolysis bullosa

C. Bodemer, A. Hovnanian, M. Titeux, 2008, Human mutation.

Childhood epidermal necrolysis and erythema multiforme major: a multicentre French cohort study of 62 patients

C. Bodemer, F. Boralevi, N. Bellon, 2021, Journal of the European Academy of Dermatology and Venereology : JEADV.

Supportive care in the acute phase of Stevens–Johnson syndrome and toxic epidermal necrolysis: an international, multidisciplinary Delphi‐based consensus

R. Stern, C. Bodemer, L. French, 2021, The British journal of dermatology.

Efficacy of the Janus kinase 1/2 inhibitor ruxolitinib in the treatment of vasculopathy associated with TMEM173-activating mutations in 3 children.

F. Rieux-Laucat, A. Fischer, C. Bodemer, 2016, The Journal of allergy and clinical immunology.

Non-penetrating deep sclerectomy for glaucoma associated with Sturge-Weber syndrome.

C. Bodemer, C. Orssaud, M. Bourgeois, 2006, Acta ophthalmologica Scandinavica.

Management of ocular involvement in the acute phase of Stevens-Johnson syndrome and toxic epidermal necrolysis: french national audit of practices, literature review, and consensus agreement

C. Bodemer, O. Dereure, P. Wolkenstein, 2020, Orphanet Journal of Rare Diseases.

Cutaneous Adverse Events in Renal Transplant Recipients Receiving Sirolimus-Based Therapy1

C. Bodemer, M. Mamzer-Bruneel, E. Morelon, 2005, Transplantation.

Mycosis fungoides following pityriasis lichenoides: An exceptional event or a potential evolution?

C. Bodemer, N. Brousse, O. Boccara, 2012, Pediatric blood & cancer.

Segmental and nonsegmental childhood vitiligo has distinct clinical characteristics: a prospective observational study.

C. Bodemer, S. Barbarot, Pierre Vabres, 2010, Journal of the American Academy of Dermatology.

Supportive Care: Bathing, Wound Care, Nutrition, Pain and Itch Management, Psychosocial Support, Palliation

C. Bodemer, D. Murrell, A. Diem, 2015 .

Skin expression of metalloproteinases and tissue inhibitor of metalloproteinases in sibling patients with recessive dystrophic epidermolysis and intrafamilial phenotypic variation.

C. Bodemer, G. Godeau, Y. de Prost, 2003, The Journal of investigative dermatology.

Deletions within COL7A1 exons distant from consensus splice sites alter splicing and produce shortened polypeptides in dominant dystrophic epidermolysis bullosa.

C. Bodemer, M. Lathrop, Y. Barrandon, 1998, American journal of human genetics.

DNA-based prenatal diagnosis of generalized recessive dystrophic epidermolysis bullosa in six pregnancies at risk for recurrence.

J. Terwilliger, C. Bodemer, A. Christiano, 1995, The Journal of investigative dermatology.

Hand surgery in recessive dystrophic epidermolysis bullosa: Our experience with dermal substitutes.

C. Bodemer, S. Leclerc-Mercier, S. Guero, 2021, Journal of plastic, reconstructive & aesthetic surgery : JPRAS.

Hologene 5: A Phase II/III Clinical Trial of Combined Cell and Gene Therapy of Junctional Epidermolysis Bullosa

C. Bodemer, M. De Luca, L. De Rosa, 2021, Frontiers in Genetics.

Sex‐ and age‐adjusted prevalence estimates of five chronic inflammatory skin diseases in France: results of the « OBJECTIFS PEAU » study

C. Bodemer, L. Misery, M. Richard, 2018, Journal of the European Academy of Dermatology and Venereology : JEADV.

Efficacy and safety of Oleogel-S10 (birch triterpenes) for epidermolysis bullosa: results from the phase III randomized double-blind phase of the EASE study.

C. Bodemer, E. Sprecher, D. Murrell, 2022, The British journal of dermatology.

Proliferative Nodules vs Melanoma Arising in Giant Congenital Melanocytic Nevi During Childhood.

C. Bodemer, J. Merlio, F. Boralevi, 2016, JAMA dermatology.

Development and co-construction of a therapeutic patient education program for albinism.

C. Bodemer, S. Hadj-Rabia, S. Compain, 2021, Annales de dermatologie et de venereologie.

BRAF Mutation Correlates With High-Risk Langerhans Cell Histiocytosis and Increased Resistance to First-Line Therapy.

Valérie Rigau, Valérie Taly, Christine Bodemer, 2016, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Dento-Craniofacial Phenotypes and underlying Molecular Mechanisms in Hypohidrotic Ectodermal Dysplasia (HED): a Review

C. Bodemer, M. Schmittbuhl, F. Clauss, 2008, Journal of dental research.

X‐linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic‐dental phenotypic findings

A. Smahi, C. Bodemer, P. Calvas, 2010, Clinical genetics.

Craniofacial bone atrophy in Parry Romberg syndrome demonstrated using a Bayesian hierarchical model.

C. Bodemer, Q. Hennocq, R. Khonsari, 2019, Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery.

Cutaneous carcinoma during long-term hydroxyurea therapy: a report of 5 cases.

C. Bodemer, O. Chosidow, Y. de Prost, 1996, Archives of dermatology.

Protocol for the Phase 2 EDELIFE Trial Investigating the Efficacy and Safety of Intra-Amniotic ER004 Administration to Male Subjects with X-Linked Hypohidrotic Ectodermal Dysplasia

C. Bodemer, A. Clarke, H. Schneider, 2023, Genes.

Automatic recognition of the XLHED phenotype from facial images

C. Bodemer, O. Klein, H. Schneider, 2017, American journal of medical genetics. Part A.

Mutations in ACTRT1 and its enhancer RNA elements lead to aberrant activation of Hedgehog signaling in inherited and sporadic basal cell carcinomas

G. Gyapay, A. Smahi, C. Bodemer, 2017, Nature Medicine.

Langerhans Cell Histiocytoma: A Benign Histiocytic Neoplasm of Diverse Lines of Terminal Differentiation

T. Molina, C. Bodemer, J. Emile, 2019, The American Journal of dermatopathology.

[Cutaneous transformation of chronic lymphoid leukemia into immunoblastic lymphoma. Cutaneous manifestation of Richter syndrome].

C. Bodemer, N. Brousse, P. Rousselot, 1995, Annales de dermatologie et de venereologie.

Burden of adult neurofibromatosis 1: development and validation of a burden assessment tool

C. Bodemer, M. Bennani, A. Bourgeois, 2019, Orphanet Journal of Rare Diseases.

New mechanism of X-linked anhidrotic ectodermal dysplasia with immunodeficiency: impairment of ubiquitin binding despite normal folding of NEMO protein.

A. Fischer, C. Bodemer, J. Casanova, 2011, Blood.

A hypermorphic IκBα mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency

A. Fischer, F. Deist, A. Smahi, 2003 .

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling

A. Fischer, F. Deist, A. Smahi, 2001, Nature Genetics.

Epithelial barrier dysfunction in desmoglein-1 deficiency.

A. Smahi, C. Bodemer, A. Munnich, 2018, The Journal of allergy and clinical immunology.

Interleukin-36-receptor antagonist deficiency and generalized pustular psoriasis.

A. Smahi, C. Bodemer, A. Munnich, 2011, The New England journal of medicine.

Congenital fibroblastic connective tissue nevi: Unusual and misleading presentations in three infantile cases

C. Bodemer, M. Mitrofanoff, R. Khonsari, 2018, Pediatric dermatology.

Lack of interaction between NEMO and SHARPIN impairs linear ubiquitination and NF‐&kgr;B activation and leads to incontinentia pigmenti

A. Smahi, C. Bodemer, A. Munnich, 2017, The Journal of allergy and clinical immunology.

Clinical study of 40 cases of incontinentia pigmenti.

A. Smahi, C. Bodemer, S. Hadj-Rabia, 2003, Archives of dermatology.

Treatment of cutaneous lymphoid hyperplasia with thalidomide: report of two cases.

C. Bodemer, M. Bagot, J. Revuz, 1999, Journal of the American Academy of Dermatology.

Malignant Melanoma Arising in Patients with a Large Congenital Melanocytic Naevus: Retrospective Study of 10 Cases with Cytogenetic Analysis.

C. Bodemer, N. Dupin, M. Avril, 2015, Acta dermato-venereologica.

Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping.

L. Cardon, C. Bodemer, D. Kelsell, 2000, American Journal of Human Genetics.

Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome

C. Bodemer, P. Houillier, P. Curmi, 2017, Genetics in Medicine.

University of Groningen Supportive care in the acute phase of Stevens-Johnson syndrome and toxic epidermal necrolysis

R. Stern, C. Bodemer, A. Paller, 2021 .

Differentiation of Langerhans cells in Langerhans cell histiocytosis.

C. Bodemer, F. Geissmann, N. Brousse, 2001, Blood.

Safe use of ketamine for acute pain in children suffering from major epidermolysis bullosa (EB)

C. Bodemer, P. Carli, C. Télion, 2000 .

Practical management of epidermolysis bullosa: consensus clinical position statement from the European Reference Network for Rare Skin Diseases

C. Bodemer, C. Sălăvăstru, C. Has, 2021, Journal of the European Academy of Dermatology and Venereology : JEADV.

Rapamycin inhibits growth and survival of D816V-mutated c-kit mast cells.

C. Bodemer, Aurélie Hermant, R. Liblau, 2006, Blood.

X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production

C. Bodemer, J. Casanova, A. Israël, 2006, The Journal of experimental medicine.

Insight into IKBKG/NEMO Locus: Report of New Mutations and Complex Genomic Rearrangements Leading to Incontinentia Pigmenti Disease

A. Smahi, C. Bodemer, A. Munnich, 2014, Human mutation.

Mast cell sarcoma: new cases and literature review

M. Soussan, C. Bodemer, P. Dubreuil, 2016, Oncotarget.

Clinical expression and new SPINK5 splicing defects in Netherton syndrome: unmasking a frequent founder synonymous mutation and unconventional intronic mutations.

C. Bodemer, A. Hovnanian, A. Stratigos, 2012, The Journal of investigative dermatology.

Therapeutic plasma exchange for life‐threatening pediatric disorders

C. Bodemer, C. Elie, R. Salomon, 2021, Journal of clinical apheresis.

Rapamycin‐associated lymphoedema in an infant with Kasabach–Merritt phenomenon

C. Bodemer, S. Hadj-Rabia, O. Boccara, 2016, The British journal of dermatology.

Inherited Immunodeficiency: A New Association With Early-Onset Childhood Panniculitis

F. Rieux-Laucat, C. Bodemer, B. Bader-Meunier, 2018, Pediatrics.

Scalp nodules as a presenting sign of fibrodysplasia ossificans progressiva: a register-based study.

C. Bodemer, Y. de Prost, M. le Merrer, 2011, Journal of the American Academy of Dermatology.

Osteopetrosis, lymphedema, anhidrotic ectodermal dysplasia, and immunodeficiency in a boy and incontinentia pigmenti in his mother.

A. Fischer, A. Smahi, G. Courtois, 2002, Pediatrics.

Retiform hemangioendothelioma developed on the site of an earlier cystic lymphangioma in a six-year-old girl.

C. Bodemer, N. Brousse, E. Calonje, 2011, The American Journal of dermatopathology.

Cutaneous Richter’s Syndrome, Prognosis, and Clinical, Histological and Immunohistological Patterns: Report of Four Cases and Review of the Literature

C. Bodemer, N. Brousse, O. Hermine, 2010, Dermatology.

Short‐ and medium‐term efficacy of specific hydrotherapy in inherited ichthyosis

C. Bodemer, S. Barbarot, F. Boralevi, 2011, The British journal of dermatology.

Severe cutaneous papillomavirus disease after haemopoietic stem-cell transplantation in patients with severe combined immune deficiency caused by common γc cytokine receptor subunit or JAK-3 deficiency

A. Fischer, F. Deist, C. Bodemer, 2004, The Lancet.

Major response to imatinib and chemotherapy in a newborn patient prenatally diagnosed with generalized infantile myofibromatosis

C. Bodemer, D. Orbach, G. Pierron, 2020, Pediatric blood & cancer.

Infantile myofibromatosis: a series of 28 cases.

Christine Bodemer, C. Bodemer, A. Harroche, 2014, Journal of the American Academy of Dermatology.

Serious childhood angiomas: unsuccessful alpha‐2b interferon treatment. A report of four cases

C. Bodemer, G. Sebag, F. Brunelle, 1993, The British journal of dermatology.

Genetic characterization of congenital tufting enteropathy: epcam associated phenotype and involvement of SPINT2 in the syndromic form

A. Smahi, C. Bodemer, A. Munnich, 2014, Human Genetics.

From Diagnosis to Prognosis: Revisiting the Meaning of Muscle ISG15 Overexpression in Juvenile Inflammatory Myopathies

C. Bodemer, M. Rodero, G. Rice, 2020, Arthritis & rheumatology.

A new lamin a mutation associated with acrogeria syndrome.

C. Bodemer, N. Lévy, S. Hadj-Rabia, 2014, The Journal of investigative dermatology.

[Photosensitivity in children].

C. Bodemer, N. Bodak, 2002, Annales de dermatologie et de vénéréologie.

Subcutaneous Panniculitis-like T-Cell Clonal Proliferation in an Infant. Lymphoma or Reactive Lymphoproliferation?

C. Bodemer, N. Brousse, B. Bader-Meunier, 2014 .

Disease‐associated mutations identify a novel region in human STING necessary for the control of type I interferon signaling

F. Rieux-Laucat, C. Bodemer, C. Wouters, 2017, The Journal of allergy and clinical immunology.

Turkish Ectodermal Dysplasia Cohort: From Phenotype to Genotype in 17 Families

A. Smahi, C. Bodemer, H. Kayserili, 2019, Cytogenetic and Genome Research.

Kaposi’s sarcoma in a child with Wiskott-Aldrich syndrome

A. Fischer, F. Deist, C. Bodemer, 2006, European Journal of Pediatrics.

Moderate and transient transfusion-associated cutaneous graft-versus-host disease in a child infected by human immunodeficiency virus.

C. Bodemer, S. Blanche, C. Raffoux, 1996, The American journal of medicine.

Primary cutaneous Epstein-Barr virus-related lymphoproliferative disorders in 4 immunosuppressed children.

C. Bodemer, N. Brousse, S. Blanche, 2008, Journal of the American Academy of Dermatology.

A novel form of syndromic cutis laxa with facial dysmorphism, cleft palate, and mental retardation

C. Bodemer, A. Munnich, A. Verloes, 2004, Journal of Medical Genetics.

Connective tissue nevi: an entity revisited.

C. Bodemer, A. Picard, Y. de Prost, 2012, Journal of the American Academy of Dermatology.

Skin biopsy is helpful in the diagnosis of hereditary fibrosing POIKiloderma with tendon contractures, myopathy and pulmonary fibrosis, due to FAM111B mutation

C. Bodemer, S. Mercier, S. Barbarot, 2022, Journal of the European Academy of Dermatology and Venereology : JEADV.

Tibial Lymphoplasmacytic Plaque: A New, Illustrative Case of a Recently and Poorly Recognized Benign Lesion in Children

C. Bodemer, S. Hadj-Rabia, S. Fraitag, 2012, Dermatology.

Eosinophilic esophagitis and colonic mucosal eosinophilia in Netherton syndrome.

C. Bodemer, S. Hadj-Rabia, C. Dupont, 2017, The Journal of allergy and clinical immunology.

Clinical spectrum of tufted angiomas in childhood: a report of 13 cases and a review of the literature.

C. Bodemer, S. Hadj-Rabia, Y. de Prost, 2010, Archives of dermatology.

Clinical Spectrum of Tufted Angiomas in Childhood

C. Bodemer, S. Hadj-Rabia, Y. Prost, 2010 .

The effects of sirolimus on Kasabach–Merritt phenomenon coagulopathy

C. Bodemer, T. Leblanc, S. Hadj-Rabia, 2018, The British journal of dermatology.

Successful treatment of Kasabach-Merritt syndrome with pentoxifylline.

C. Bodemer, Y. de Prost, D. de Prost, 1991, Journal of the American Academy of Dermatology.

Acne Fulminans: Case Series and Review of the Literature

C. Bodemer, A. Alakeel, N. Auffret, 2016, Pediatric dermatology.

Carrying out local care for epidermal necrolysis: survey of practices

C. Bodemer, O. Dereure, C. Bernier, 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.

Genetic bases of severe junctional epidermolysis bullosa presenting spontaneous amelioration with aging.

C. Bodemer, J. Ortonne, Y. Prost, 2001, Human molecular genetics.

Clinical and histologic features of incontinentia pigmenti in adults with nuclear factor-κB essential modulator gene mutations.

A. Smahi, C. Bodemer, S. Hadj-Rabia, 2011, Journal of the American Academy of Dermatology.

Skin biopsy is helpful for the diagnosis of incontinentia pigmenti at late stage (IV): a series of 26 cutaneous biopsies

C. Bodemer, N. Brousse, S. Hadj-Rabia, 2009, Journal of cutaneous pathology.

[Melanoma in children: diagnosis and treatment specificities].

C. Bodemer, M. Avril, S. Fraitag, 2012, Bulletin du cancer.

Syndromic (phenotypic) diarrhea in early infancy

C. Bodemer, N. Brousse, O. Goulet, 2008, Orphanet journal of rare diseases.

The histopathological spectrum of cutaneous meningeal heterotopias: clues and pitfalls

C. Bodemer, C. Fallet-Bianco, N. Brousse, 2011, Histopathology.

Orphanet Journal of Rare Diseases Syndromic (phenotypic) Diarrhea in Early Infancy Background

C. Bodemer, N. Brousse, O. Goulet, 2022 .

Phenotypic and Genotypic Characteristics of Mastocytosis According to the Age of Onset

Olivier Hermine, Felipe Suarez, Christine Bodemer, 2008, PloS one.

Molecular basis of the spectral expression of CIAS1 mutations associated with phagocytic cell-mediated autoinflammatory disorders CINCA/NOMID, MWS, and FCU.

A. Fischer, C. Bodemer, G. Morgan, 2004, Blood.

[Nodular fasciitis of childhood: a clinicopathological analysis of 10 cases].

C. Bodemer, N. Brousse, J. Dauendorffer, 2008, Annales de dermatologie et de venereologie.

Cutaneous malignant melanoma in children and adolescents treated in pediatric oncology units

C. Bodemer, C. Robert, D. Orbach, 2016, Pediatric blood & cancer.

Heterozygous PDGFRB Mutation in a Three-generation Family with Autosomal Dominant Infantile Myofibromatosis.

Christine Bodemer, C. Bodemer, S. Hadj-Rabia, 2017, Acta dermato-venereologica.

Myogenic Progenitor Cells Exhibit Type I Interferon–Driven Proangiogenic Properties and Molecular Signature During Juvenile Dermatomyositis

C. Bodemer, S. Germain, D. Duffy, 2018, Arthritis & rheumatology.

Human T-cell lymphotropic virus-1-positive T-cell leukemia/lymphoma in a child. Report of a case and review of the literature.

C. Bodemer, A. Székely, L. Medeiros, 1997, Archives of pathology & laboratory medicine.

Sustained complete cytologic and molecular remission induced by donor leucocyte infusions alone in an acute myeloblastic leukaemia in relapse after bone marrow transplantation

C. Bodemer, O. Hermine, V. Ribrag, 1996, British journal of haematology.

Kawasaki disease: an unexpected etiology of shock and multiple organ dysfunction syndrome

C. Bodemer, F. Lesage, L. Dupic, 2012, Intensive Care Medicine.

Paediatric mastocytosis: a systematic review of 1747 cases

C. Bodemer, P. Dubreuil, G. Damaj, 2015, The British journal of dermatology.

Multidisciplinary consensus recommendations from a European network for the diagnosis and practical management of patients with incontinentia pigmenti

C. Bodemer, F. Fusco, M. de La Dure-Molla, 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.

A case of reversible pulmonary arterial hypertension associated with incontinentia pigmenti

C. Bodemer, B. Neven, D. Bonnet, 2018, Pulmonary circulation.

Postzygotic mosaicism and incontinentia pigmenti in male patients: molecular diagnosis yield

C. Bodemer, S. Hadj-Rabia, J. Steffann, 2018, The British journal of dermatology.

Severe neuroimaging anomalies are usually associated with random X inactivation in leucocytes circulating DNA in X-linked dominant Incontinentia Pigmenti.

A. Smahi, C. Bodemer, A. Munnich, 2017, Molecular genetics and metabolism.

Use of Epidermal Growth Factor Receptor Inhibitor Erlotinib to Treat Palmoplantar Keratoderma in Patients With Olmsted Syndrome Caused by TRPV3 Mutations.

T. Molina, C. Bodemer, S. Hadj-Rabia, 2020, JAMA dermatology.

Atopic dermatitis burden scale: creation of a specific burden questionnaire for families

C. Bodemer, N. Perez-Cullell, S. Branchoux, 2013, Journal of the European Academy of Dermatology and Venereology : JEADV.

Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity

C. Bodemer, M. Kempers, A. Plomp, 2013, Orphanet Journal of Rare Diseases.

Pain and quality of life evaluation in patients with localized epidermolysis bullosa simplex

C. Bodemer, C. Chiaverini, S. Mallet, 2017, Orphanet Journal of Rare Diseases.

Persistent Mycobacterium marinum infection in a child with probable visceral involvement.

C. Bodemer, J. Gaillard, S. Blanche, 1990, The Pediatric Infectious Disease Journal.

A toxic palmitoylation on Cdc42 drives a severe autoinflammatory syndrome

A. Smahi, C. Bodemer, J. Casanova, 2019 .

Fibrous Arthropathy Associated With Morphea: A New Cause of Diffuse Acquired Joint Contractures

C. Bodemer, C. Wouters, J. Stéphan, 2017, Pediatrics.

Efficacy of propranolol in hepatic infantile hemangiomas with diffuse neonatal hemangiomatosis.

C. Bodemer, Pierre Vabres, J. Mazereeuw-Hautier, 2010, The Journal of pediatrics.

Haemangioma family burden: creation of a specific questionnaire.

C. Bodemer, O. Boccara, J. Voisard, 2015, Acta dermato-venereologica.

[Kasabach-Merritt syndrome in children].

C. Bodemer, G. Sebag, F. Brunelle, 1992, Annales de pediatrie.

Skin Biopsy in Netherton Syndrome: A Histological Review of a Large Series and New Findings

T. Molina, C. Bodemer, A. Hovnanian, 2016, The American Journal of dermatopathology.

[Giant congenital blue nevus of the scalp].

C. Bodemer, S. Fraitag, D. Teillac-Hamel, 1996, Annales de dermatologie et de venereologie.

CEMARA an information system for rare diseases

Mohamed Ben Saïd, Paul Landais, Jean Philippe Jaïs, 2010, MedInfo.

Adjuvant treatment with the bacterial lysate (OM-85) improves management of atopic dermatitis: A randomized study

C. Bodemer, C. la Vecchia, F. Boralevi, 2017, PloS one.

An asymptomatic subcutaneous nodule of the lower back: a sentinel lesion for a diagnosis not to be missed.

C. Bodemer, Y. de Prost, S. Fraitag, 2013, The American Journal of dermatopathology.

Nonbacterial purpura fulminans and severe autoimmune acquired protein S deficiency associated with human herpesvirus‐6 active replication

C. Bodemer, S. Pannier, O. Boccara, 2009, The British journal of dermatology.

Control of TLR7-mediated type I IFN signaling in pDCs through CXCR4 engagement—A new target for lupus treatment

Yasser B. Ruiz-Blanco, C. Bodemer, F. Kirchhoff, 2019, Science Advances.

Unusual cutaneous features associated with a heterozygous gain‐of‐function mutation in IFIH1: overlap between Aicardi‐Goutières and Singleton‐Merten syndromes

C. Bodemer, G. Rice, T. Briggs, 2015, The British journal of dermatology.

A focus on rare and undiagnosed skin diseases

C. Bodemer, M. Schmuth, J. Bauer, 2019, Experimental Dermatology.

[Scleroderma in children: a retrospective study of 70 cases].

C. Bodemer, A. Prieur, Y. de Prost, 1999, Annales de dermatologie et de venereologie.

Renal-Transplant Recipients and Sun Protection

C. Bodemer, J. Fermanian, M. Mamzer-Bruneel, 2004, Transplantation.

[Non epidermotropic T lymphoma preceded for several years by hypereosinophilic syndrome].

C. Bodemer, C. Haioun, M. Bagot, 1990, Annales de dermatologie et de venereologie.

Impact of a rare chronic genodermatosis on family daily life: the example of epidermolysis bullosa

C. Bodemer, S. Hadj-Rabia, H. Dufresne, 2018, The British journal of dermatology.

Feelings of guilt in parents of children with atopic dermatitis

C. Bodemer, S. Mallet, S. Barbarot, 2021, Journal of the European Academy of Dermatology and Venereology : JEADV.

Methotrexate in Severe Childhood Alopecia Areata: Long-term Follow-up.

C. Bodemer, S. Barbarot, Pierre Vabres, 2016, Acta dermato-venereologica.

Development and validation of an epidermolysis bullosa family/parental burden score

C. Bodemer, S. Hadj-Rabia, C. Taieb, 2015, The British journal of dermatology.

Family burden in inherited ichthyosis: creation of a specific questionnaire

C. Bodemer, S. Hadj-Rabia, V. Sibaud, 2013, Orphanet Journal of Rare Diseases.

Efficacy of topical ropivacaine in children and young adults with hereditary epidermolysis bullosa

C. Bodemer, C. Elie, N. Bellon, 2020, The British journal of dermatology.

Clinical Features, Histological Characteristics, and Disease Outcomes of Mycosis Fungoides in Children and Adolescents: A Nationwide Multicentre Cohort of 46 Patients

C. Bodemer, C. Chiaverini, O. Dereure, 2022, Dermatology.

[Childhood-onset systemic lupus erythematosus].

C. Bodemer, E. Haddad, R. Salomon, 2003, Archives de pédiatrie.

Human iPSC-derived-keratinocytes, a useful model to identify and explore pathological phenotype of Epidermolysis Bullosa Simplex.

C. Bodemer, S. Hadj-Rabia, H. Polvèche, 2022, Journal of Investigative Dermatology.

Lupus érythémateux disséminé chez l'enfant : recommandations concernant les examens à effectuer lors de l'évaluation initiale et du suivi Guidelines about investigations to be performed at the diagnosis and during the follow-up of childhood-onset systemic lupus erythematosus

C. Bodemer, E. Haddad, R. Salomon, 2004 .

Absence of circulating mast cell precursors in paediatric mastocytosis: could it reflect a different pathophysiology between adults and children with mastocytosis?

C. Bodemer, P. Dubreuil, O. Hermine, 2014, Journal of the European Academy of Dermatology and Venereology : JEADV.

[Hemophagocytic syndrome. 2 cases in children with Still's disease].

C. Bodemer, A. Prieur, J. Stéphan, 1991, Annales de dermatologie et de venereologie.

Molecular and clinicopathologic characterization of pediatric histiocytoses

C. Bodemer, A. Idbaih, J. Emile, 2023, American journal of hematology.

Perceived clinical severity of atopic dermatitis in children: comparison between patients’ and parents’ evaluation

C. Bodemer, S. Mallet, S. Barbarot, 2022, Journal of the European Academy of Dermatology and Venereology : JEADV.

Characteristics of children and adolescents with atopic dermatitis who attended therapeutic patient education

C. Bodemer, S. Mallet, S. Barbarot, 2021, Journal of the European Academy of Dermatology and Venereology : JEADV.

Pseudo purpura fulminans et primo-infection à HHV6

C. Bodemer, F. Lesage, L. Dupic, 2007 .

Neonatal and self‐healing linear immunoglobulin A dermatosis

C. Bodemer, S. Hadj-Rabia, O. Boccara, 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.

Cognitive profile of school‐age children and teenagers with hypohidrotic ectodermal dysplasia (HED)

C. Bodemer, S. Jacob, S. Hadj-Rabia, 2014, American journal of medical genetics. Part A.

Bilateral amastia in a female with X‐linked hypohidrotic ectodermal dysplasia

C. Bodemer, S. Hadj-Rabia, J. Bonnefont, 2014, The British journal of dermatology.

Efficacy and Safety of Cladribine in Adult Systemic Mastocytosis : A French Multicenter Study of 33 Patients.

C. Bodemer, J. Launay, P. Dubreuil, 2004 .

Psoriasis and obesity in French children: a case–control, multicentre study

C. Bodemer, C. Chiaverini, S. Barbarot, 2015, The British journal of dermatology.

Burden of albinism: development and validation of a burden assessment tool

C. Bodemer, M. Bennani, K. Ezzedine, 2018, Orphanet Journal of Rare Diseases.

Keratotic follicular plugs with calcifications in Conradi–Hünermann–Happle syndrome: histological, biochemical and genetic testing correlation

C. Bodemer, D. Bozon, S. Hadj-Rabia, 2015, The British journal of dermatology.

Association of mastocytosis with inflammatory joint diseases: a series of 31 patients.

C. Bodemer, V. Ugo, K. Briot, 2014, Seminars in arthritis and rheumatism.

JAK Inhibition in Aicardi-Goutières Syndrome: a Monocentric Multidisciplinary Real-World Approach Study

C. Bodemer, N. Boddaert, D. Duffy, 2023, Journal of Clinical Immunology.

French data on the epidemiology and expert healthcare network for epidermolysis bullosa

C. Bodemer, L. Soussand, A. Jannot, 2022, Journal of the European Academy of Dermatology and Venereology : JEADV.

Genotypic and phenotypic analysis of 34 cases of inherited junctional epidermolysis bullosa caused by COL17A1 mutations

C. Bodemer, C. Chiaverini, S. Hadj-Rabia, 2021, The British journal of dermatology.

Wound closure in epidermolysis bullosa: data from the vehicle arm of the phase 3 ESSENCE Study

C. Bodemer, A. Paller, D. Murrell, 2020, Orphanet Journal of Rare Diseases.

Multidisciplinary care of epidermolysis bullosa during the COVID-19 pandemic—Consensus: Recommendations by an international panel of experts

C. Bodemer, J. Uitto, E. Sprecher, 2020, Journal of the American Academy of Dermatology.

Safety and immunogenicity of Fc‐EDA, a recombinant ectodysplasin A1 replacement protein, in human subjects

C. Bodemer, O. Klein, A. Clarke, 2020, British journal of clinical pharmacology.

Accurate diagnosis of acute hemorrhagic edema of infancy: a French multicenter observational study.

C. Bodemer, C. Chiaverini, S. Mallet, 2023, European journal of pediatrics.

Probable DRESS syndrome induced by IL-1 inhibitors

C. Bodemer, B. Bader-Meunier, P. Quartier, 2017, Orphanet Journal of Rare Diseases.

Clinical variability and probable founder effect in oculocutaneous albinism type 7

C. Bodemer, A. Harroche, S. Hadj-Rabia, 2019, Clinical Genetics.

Acitretin in Children

C. Bodemer, Y. Prost, D. Teillac, 1991 .

Lymphoedema is a potential sequela of Kaposiform haemangioendothelioma: reply from the authors

C. Bodemer, S. Hadj-Rabia, O. Boccara, 2016, The British journal of dermatology.

A familial T-cell lymphoma with gamma delta phenotype and an original location. Possible role of chronic Epstein-Barr virus infection.

S. Schraub, C. Bodemer, F. Sigaux, 1996, Cancer.

Unexpected extradermatological findings in 31 patients with xeroderma pigmentosum type C

C. Bodemer, S. Mallet, B. Grandchamp, 2013, The British journal of dermatology.

DOCK11 deficiency in patients with X-linked actinopathy and autoimmunity.

F. Rieux-Laucat, C. Bodemer, C. Picard, 2023, Blood.

[Anaphylaxis syndrome induced by exercise].

C. Bodemer, J. de Blic, P. Scheinmann, 1989, Archives francaises de pediatrie.

Early management of sight threatening retinopathy in incontinentia pigmenti

C. Bodemer, S. Hadj-Rabia, D. Bremond-Gignac, 2020, Orphanet Journal of Rare Diseases.

Respiratory complications in pediatric epidermal necrolysis: a retrospective study of 22 cases.

C. Delacourt, C. Bodemer, N. Garcelon, 2023, Journal of the American Academy of Dermatology.

The Burden of Autosomal Recessive Congenital Ichthyoses on Patients and their Families: An Italian Multicentre Study

C. Bodemer, D. Bonamonte, A. Filoni, 2021, Acta dermato-venereologica.

Cutaneous location of atypical teratoid/rhabdoid tumour.

C. Bodemer, T. Roujeau, L. Salomon, 2014, Acta dermato-venereologica.

Chronic Mucocutaneous Candidiasis in Humans with Inborn Errors of Interleukin-17 Immunity

C. Bodemer, J. Casanova, C. Picard, 2011, Science.

Familial benign chronic pemphigus and doxycycline: a review of 6 cases

C. Bodemer, S. Fraitag, E. Raynaud, 2014, Journal of the European Academy of Dermatology and Venereology.

Br Ief Definitive Repor T Autoantibodies against Il-17a, Il-17f, and Il-22 in Patients with Chronic Mucocutaneous Candidiasis and Autoimmune Polyendocrine Syndrome Type I Most Patients with Autoimmune Polyendocrine Syndrome Type I (aps-i) Display Chronic Mucocu- Taneous Candidiasis (cmc). We Hypothe

A. Fischer, R. Döffinger, C. Bodemer, 2022 .

Alterations of the IKBKG locus and diseases: an update and a report of 13 novel mutations

M. D'urso, A. Smahi, C. Bodemer, 2008, Human mutation.

Erratum: Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis (Nature Genetics (2009) 41 (228-233))

S. Cichon, M. Nöthen, C. Bodemer, 2009 .

Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases

A. Smahi, C. Bodemer, A. Munnich, 2011, Human mutation.

Does surgery of lymphatic malformations lead to an increase in superficial lymphangiectasia? A retrospective study of 43 patients

C. Bodemer, S. Pannier, A. Schreiber, 2019, The British journal of dermatology.

Epithelial barrier dysfunction in desmoglein-1 deficiency.

A. Smahi, C. Bodemer, A. Munnich, 2018, The Journal of allergy and clinical immunology.

Eosinophilic esophagitis and colonic mucosal eosinophilia in Netherton syndrome.

C. Bodemer, S. Hadj-Rabia, C. Dupont, 2017, The Journal of allergy and clinical immunology.

A New Patient with p40phox Deficiency and Chronic Immune Thrombocytopenia

C. Bodemer, J. Casanova, R. Lévy, 2023, Journal of Clinical Immunology.

[Acute hemorrhagic edema of infancy associated with Coxsackie virus infection].

C. Bodemer, C. Bodemer, P. Foucaud, 2017, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Identification of new RECQL4 mutations in Caucasian Rothmund-Thomson patients and analysis of sensitivity to a wide range of genotoxic agents.

C. Bodemer, S. Queillé, A. Sarasin, 2008, Mutation research.