K. Dahan

发表

L. Morando, D. Kahila, A. Vénisse, 2011, Pediatric Nephrology.

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders

Davis J. McCarthy, Calliope A. Dendrou, Lisa J. Murray, 2015, Nature Genetics.

Tamm-Horsfall protein or uromodulin: new ideas about an old molecule.

K. Dahan, O. Devuyst, Y. Pirson, 2005, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Identification of novel and recurrent glucokinase mutations in Belgian and Luxembourg maturity onset diabetes of the young patients

C. de Beaufort, Raoul Rooman, C. Mathieu, 2006, Clinical genetics.

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

Corinne Antignac, K. Dahan, O. Gribouval, 2000, Nature Genetics.

Rituximab for Severe Membranous Nephropathy: A 6-Month Trial with Extended Follow-Up.

K. Dahan, A. Rousseau, T. Simon, 2017, Journal of the American Society of Nephrology : JASN.

Impact of polymorphism of Multidrug Resistance-associated Protein 1 (ABCC1) gene on the severity of cystic fibrosis.

P. Lebecque, K. Dahan, A. Mafficini, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Hepatitis B virus reactivation during belatacept treatment after kidney transplantation

K. Dahan, L. Mesnard, A. Canestri, 2019, Transplant infectious disease : an official journal of the Transplantation Society.

Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management--A KDIGO consensus report.

K. Dahan, C. Antignac, M. Wolf, 2015, Kidney international.

C‐mip interacts with the p85 subunit of PI3 kinase and exerts a dual effect on ERK signaling via the recruitment of Dip1 and DAP kinase

K. Dahan, M. Kamal, D. Sahali, 2010, FEBS letters.

B- and T-cell subpopulations in patients with severe idiopathic membranous nephropathy may predict an early response to rituximab.

K. Dahan, D. Klatzmann, T. Simon, 2017, Kidney international.

Abstracts presented at the 23rd Annual Congress of the Belgian Society of Internal Medicine, 14–15 December 2018, Dolce La Hulpe, La Hulpe, Belgium

D. Abramowicz, K. Dahan, K. Claes, 2018, Acta clinica Belgica.

Clinical and Genetic Spectra of Autosomal Dominant Tubulointerstitial Kidney Disease due to Mutations in UMOD and MUC1.

K. Dahan, T. Fehr, D. Gale, 2020, Kidney international.

Membranous Nephropathy Associated With Immunological Disorder-Related Liver Disease

N. Rioux-Leclercq, K. Dahan, E. Daugas, 2015, Medicine.

Prognostic value of PLA2R autoimmunity detected by measurement of anti-PLA2R antibodies combined with detection of PLA2R antigen in membranous nephropathy: A single-centre study over 14 years

K. Dahan, H. Debiec, I. Brochériou, 2017, PloS one.

Phenotype and outcome in hereditary tubulointerstitial nephritis secondary to UMOD mutations.

K. Dahan, C. Antignac, D. Lacombe, 2011, Clinical journal of the American Society of Nephrology : CJASN.

Anti TNF-α in refractory Takayasu's arteritis: cases series and review of the literature.

K. Dahan, Z. Amoura, J. Emmerich, 2012, Autoimmunity reviews.

C-mip interacts physically with RelA and inhibits nuclear factor kappa B activity.

K. Dahan, G. Guellaen, M. Kamal, 2009, Molecular immunology.

c-mip Impairs Podocyte Proximal Signaling and Induces Heavy Proteinuria

K. Dahan, M. Kamal, D. Sahali, 2010, Science Signaling.

Small glomeruli in WAGR (Wilms Tumor, Aniridia, Genitourinary Anomalies and Mental Retardation) syndrome.

N. Brousse, K. Dahan, M. Gubler, 2007, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Telomere length, ATM mutation status and cancer risk in Ataxia-Telangiectasia families

K. Dahan, D. Stoppa-Lyonnet, B. Gilbert-Dussardier, 2017, Carcinogenesis.

Improving mutation screening in familial hematuric nephropathies through next generation sequencing.

K. Dahan, C. Antignac, C. Bole-Feysot, 2014, Journal of the American Society of Nephrology : JASN.

Rituximab in Patients With Phospholipase A2 Receptor–Associated Membranous Nephropathy and Severe CKD

K. Dahan, J. Boffa, P. Fiévet, 2019, Kidney international reports.

Phospholipase A2 Receptor 1 Epitope Spreading at Baseline Predicts Reduced Likelihood of Remission of Membranous Nephropathy.

K. Dahan, A. Rousseau, G. Lambeau, 2017, Journal of the American Society of Nephrology : JASN.

Urinary mRNA for the Diagnosis of Renal Allograft Rejection: The Issue of Normalization

K. Dahan, F. Terzi, E. Rondeau, 2016, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Efficacy of Rituximab in a Patient With Partial Clinical Remission and Persistent Circulating PLA2R-Ab

K. Dahan, H. Debiec, P. Ronco, 2019, Kidney international reports.

The Role of PLA2R Antibody in Treatment of Membranous Nephropathy

K. Dahan, H. Debiec, P. Ronco, 2017, Kidney international reports.

Membranous glomerulonephritis: a step forward in B-cell targeting therapy?

K. Dahan, J. Boffa, 2020, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

High-Dose Rituximab and Early Remission in PLA2R1-Related Membranous Nephropathy.

K. Dahan, A. Rousseau, G. Lambeau, 2019, Clinical journal of the American Society of Nephrology : CJASN.

Rituximab Treatment for Membranous Nephropathy: A French Clinical and Serological Retrospective Study of 28 Patients

K. Dahan, E. Daugas, S. de Seigneux, 2011, Nephron Extra.

Pathological splice mutations outside the invariant AG/GT splice sites of BRCA1 exon 5 increase alternative transcript levels in the 5′ end of the BRCA1 gene

J. Vandesompele, K. Dahan, K. Claes, 2002, Oncogene.

Arteriolar Hyalinization Predicts Delayed Graft Function in Deceased Donor Renal Transplantation

F. Roudot-thoraval, K. Dahan, E. Thervet, 2008, Transplantation.

Intracranial Nocardia recurrence during fluorinated quinolones therapy

K. Dahan, M. Delahousse, M. Venditto, 2006, Transplant infectious disease : an official journal of the Transplantation Society.

Functional classification of ATM variants in ataxia‐telangiectasia patients

T. Dörk, M. Stern, P. Calvas, 2019, Human mutation.

Expanding the clinical spectrum of congenital nephrotic syndrome caused by NPHS1 mutations.

K. Dahan, N. Godefroid, 2010, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Persistent developmental delay despite successful bone marrow transplantation for purine nucleoside phosphorylase deficiency.

K. Dahan, M. Vincent, C. Vermylen, 2002, Journal of pediatric hematology/oncology.

Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants of COH1

D. Horn, K. Dahan, M. Holder-Espinasse, 2009, Human mutation.

Outcome of kidney transplantation in type Ioral‐facial‐digital syndrome

K. Dahan, C. Thauvin-Robinet, O. Devuyst, 2011, Transplant international : official journal of the European Society for Organ Transplantation.

Long-term efficacy and safety of rituximab in IgG4-related disease: Data from a French nationwide study of thirty-three patients

K. Dahan, J. Berthelot, N. Costedoat-Chalumeau, 2017, PloS one.

Non-Randall proliferative glomerulonephritis with humps and monotypic IgG deposits in primary Sjögren’s syndrome: a first case report

K. Dahan, P. Callard, J. Arlet, 2010, NDT plus.

Steroids: A Therapeutic Option for COVID-19 Pneumonia Patients With ESRD?

K. Dahan, E. Letavernier, H. François, 2020, Kidney International Reports.

The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome

Golder N Wilson, A. V. Vulto-van Silfhout, R. Pfundt, 2018, Genetics in Medicine.

High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults.

K. Dahan, P. Houillier, X. Jeunemaître, 2019, Kidney international.

Contribution of High-throughput sequencing to the Diagnosis of tubulopathies and Familal Hypercalcemia Hypocalciuria in Adults

Favero, K. Dahan, P. Houillier, 2019 .

Paradoxical embolism following thromboaspiration of an arteriovenous fistula thrombosis: a case report

A. Maraval, A. Duval, K. Dahan, 2010, Journal of medical case reports.

Constitutional mismatch repair deficiency–associated brain tumors: report from the European C4CMMRD consortium

P. Varlet, F. Andreiuolo, L. Guerrini-Rousseau, 2018, Neuro-oncology advances.

Renal transplantation from extended criteria cadaveric donors: problems and perspectives overview

K. Dahan, P. Grimbert, P. Lang, 2007, Transplant international : official journal of the European Society for Organ Transplantation.

A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes

W. Foulkes, M. Jackson, K. Dahan, 2019, Human mutation.

The Regulatory/Cytotoxic Graft-Infiltrating T Cells Differentiate Renal Allograft Borderline Change From Acute Rejection

F. Roudot-thoraval, K. Dahan, P. Grimbert, 2007, Transplantation.

Identification of an NPHP1 deletion causing adult form of nephronophthisis

K. Dahan, B. Grisart, V. Benoit, 2016, Irish Journal of Medical Science (1971 -).

Paradoxical response to furosemide in uromodulin-associated kidney disease.

K. Dahan, O. Devuyst, Y. Pirson, 2015, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia.

K. Dahan, O. Devuyst, N. Knoers, 2015, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Apixaban Prophylactic Anticoagulation in Patients with Nephrotic Syndrome

K. Dahan, J. Boffa, I. Elalamy, 2021, TH open : companion journal to thrombosis and haemostasis.

Novel COL4A1 mutations associated with HANAC syndrome: A role for the triple helical CB3[IV] domain

F. Gekeler, K. Dahan, M. Pâques, 2010, American journal of medical genetics. Part A.

Original Evaluating PVALB as a candidate gene for SLC12A3 -negative cases of Gitelman’s syndrome

K. Dahan, A. Blanchard, X. Jeunemaître, 2008 .

Spectrum of mutations in Gitelman syndrome.

D. Kahila, A. Vénisse, K. Dahan, 2011, Journal of the American Society of Nephrology : JASN.

Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood.

P. Calvas, N. Chassaing, K. Dahan, 2011, Kidney international.

Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies.

A. Vénisse, K. Dahan, X. Jeunemaître, 2018, Kidney international.

Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome

A. V. Vulto-van Silfhout, R. Pfundt, B. D. de Vries, 2019, Genetics in Medicine.

Failure of anti-CD20 monoclonal antibody therapy to prevent antibody-mediated rejection in three crossmatch-positive renal transplant recipients.

K. Dahan, P. Grimbert, V. Audard, 2007, Transplantation proceedings.

Molecular analysis of GB virus C isolates in Belgian hemodialysis patients

M. Jadoul, K. Dahan, Hsin-Fu Liu, 1998, Journal of medical virology.

The genetics of familial adenomatous polyposis (FAP) and MutYH-associated polyposis (MAP).

D. Franchimont, E. Van Cutsem, K. Dahan, 2011, Acta gastro-enterologica Belgica.

The focal form of persistent hyperinsulinemic hypoglycemia of infancy: morphological and molecular studies show structural and functional differences with insulinoma.

C. Junien, C. Sempoux, K. Dahan, 2003, Diabetes.

Renal transplantation in patients with sarcoidosis: a French multicenter study.

K. Dahan, E. Thervet, N. Kamar, 2010, Clinical journal of the American Society of Nephrology : CJASN.

Mutations in SACS cause atypical and late-onset forms of ARSACS

W. Robberecht, P. van Damme, L. de Meirleir, 2010, Neurology.

Efficacy and Safety of Rituximab in Hepatitis B Virus–Associated PLA2R-Positive Membranous Nephropathy

K. Dahan, H. Debiec, I. Brochériou, 2017, Kidney international reports.

Genetic testing in the diagnosis of chronic kidney disease: recommendations for clinical practice

G. Remuzzi, K. Dahan, C. Antignac, 2021, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Long-term health-related quality of life outcomes of adults with pediatric onset of frequently relapsing or steroid-dependent nephrotic syndrome

Z. Massy, K. Dahan, E. Daugas, 2021, Journal of Nephrology.

Renal Allograft Biopsies with Borderline Changes: Predictive Factors of Clinical Outcome

F. Roudot-thoraval, K. Dahan, P. Grimbert, 2006, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Rituximab is an efficient and safe treatment in adults with steroid-dependent minimal change disease.

K. Dahan, G. Deschênes, P. Lang, 2013, Kidney international.

Outcome of Renal Transplantation in Eight Patients with Candida sp. Contamination of Preservation Fluid

K. Dahan, P. Grimbert, F. Botterel, 2008, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

De Novo Atypical Haemolytic Uremic Syndrome after Kidney Transplantation

K. Dahan, S. Aydın, A. Devresse, 2018, Case reports in nephrology.

Immunological remission in PLA2R-antibody-associated membranous nephropathy: cyclophosphamide versus rituximab.

J. Wetzels, K. Dahan, A. Rousseau, 2018, Kidney international.

NPHS2 Mutations in Steroid‐Resistant Nephrotic Syndrome: A Mutation Update and the Associated Phenotypic Spectrum

A. Mégarbané, K. Dahan, G. Mollet, 2014, Human mutation.

A cluster of mutations in the UMOD gene causes familial juvenile hyperuricemic nephropathy with abnormal expression of uromodulin.

D. Vertommen, K. Dahan, C. Antignac, 2003, Journal of the American Society of Nephrology : JASN.

Familial juvenile hyperuricemic nephropathy and autosomal dominant medullary cystic kidney disease type 2: two facets of the same disease?

K. Dahan, F. Hildebrandt, Y. Pirson, 2001, Journal of the American Society of Nephrology : JASN.

The Struggling Odyssey of Infantile Primary Hyperoxaluria

K. Dahan, G. Deschênes, K. Ismaili, 2021, Frontiers in Pediatrics.

High prevalence of GB virus C/hepatitis G virus in Kinshasa, Democratic Republic Of Congo: A phylogenetic analysis

K. Dahan, J. Desmyter, Hsin-Fu Liu, 2000, Journal of medical virology.

Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844–848

E. Zackai, G. Mortier, David T. Miller, 2017, American journal of human genetics.

Transcriptional and functional analyses of SLC12A3 mutations: new clues for the pathogenesis of Gitelman syndrome.

K. Dahan, O. Devuyst, J. Hoenderop, 2007, Journal of the American Society of Nephrology : JASN.

NPHS 2 , encoding the glomerular protein podocin , is mutated in autosomal recessive steroid-resistant nephrotic syndrome

K. Dahan, O. Gribouval, C. Antignac, 2000 .

A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracranial hypertension.

K. Dahan, O. Devuyst, C. Saint-Martin, 2006, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Hypermethylation of the 5′ CpG island of the p14ARF flanking exon 1β in human colorectal cancer displaying a restricted pattern of p53 overexpression concomitant with increased MDM2 expression

C. Sempoux, K. Dahan, A. Kartheuser, 2012, Clinical Epigenetics.

Nephrotic syndrome after infliximab treatment in a patient with ulcerative colitis.

K. Dahan, O. Corcos, Y. Bouhnik, 2015, Journal of gastrointestinal and liver diseases : JGLD.

A homozygous mutation in INVS causing juvenile nephronophthisis with abnormal reactivity of the Wnt/beta-catenin pathway.

K. Dahan, O. Devuyst, Y. Pirson, 2010, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Distinctive patterns of p53 protein expression and microsatellite instability in human colorectal cancer.

C. Sempoux, K. Dahan, A. Jouret-Mourin, 2011, Human pathology.

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis

Richard J. Thompson, N. Freimer, G. Mieli-Vergani, 1998, Nature Genetics.

Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome

K. Dahan, R. Salomon, O. Gribouval, 2018, Pediatric Nephrology.

Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes

E. Schröck, C. Lázaro, G. Capellá, 2022, The Lancet. Oncology.

Urinary transcriptomics reveals patterns associated with subclinical injury of the renal allograft.

K. Dahan, E. Rondeau, D. Anglicheau, 2018, Biomarkers in medicine.

Urinary mRNA analysis of biomarkers to epithelial mesenchymal transition of renal allograft.

K. Dahan, E. Rondeau, Y. Gorgi, 2018, Nephrologie & therapeutique.

Deletions of both alpha 5(IV) and alpha 6(IV) collagen genes in Alport syndrome and in Alport syndrome associated with smooth muscle tumours.

C. Guyot, K. Dahan, K. Leppig, 1995, Human molecular genetics.

Intragraft levels of Foxp3 mRNA predict progression in renal transplants with borderline change.

K. Dahan, C. Badoual, P. Grimbert, 2008, Journal of the American Society of Nephrology : JASN.

Evaluating PVALB as a candidate gene for SLC12A3-negative cases of Gitelman's syndrome.

K. Dahan, X. Jeunemaître, O. Devuyst, 2008, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1

K. Dahan, P. Houillier, X. Jeunemaître, 2015, Human mutation.

Belgian consensus statement on the diagnosis and management of patients with atypical hemolytic uremic syndrome

D. Abramowicz, K. Dahan, L. P. Van den Heuvel, 2018, Acta clinica Belgica.

Evidence of digenic inheritance in Alport syndrome

K. Dahan, C. Antignac, B. Knebelmann, 2015, Journal of Medical Genetics.

An Augmented ABCA4 Screen Targeting Noncoding Regions Reveals a Deep Intronic Founder Variant in Belgian Stargardt Patients

T. de Ravel, K. Dahan, M. de Rademaeker, 2015, Human mutation.

The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome

Patricia H. Wheeler, A. V. Vulto-van Silfhout, R. Pfundt, 2018, Genetics in Medicine.

Non-Mediterranean periodic fever

K. Dahan, J. Donckier, E. Delgrange, 1999, The Lancet.

A ‘silent’, new polymorphism of factor H and apparent de novo atypical haemolytic uraemic syndrome after kidney transplantation

S. Rorive, K. Dahan, P. Stordeur, 2014, BMJ Case Reports.

A classification of ductal plate malformations based on distinct pathogenic mechanisms of biliary dysmorphogenesis

C. Sempoux, P. Courtoy, K. Dahan, 2011, Hepatology.

High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers

V. Moreno, C. Lázaro, G. Capellá, 2019, Journal of Medical Genetics.

mTOR-Activating Mutations in RRAGD Are Causative for Kidney Tubulopathy and Cardiomyopathy

D. Sabatini, E. Schulze-Bahr, B. Schermer, 2021, Journal of the American Society of Nephrology : JASN.

OP-NDTJ210220 1..16

G. Remuzzi, K. Dahan, C. Antignac, 2021 .

X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study.

H. Smeets, J. Jais, M. Sanak, 2003, Journal of the American Society of Nephrology : JASN.

Early-onset of ADCK4 glomerulopathy with renal failure: a case report

K. Dahan, K. Ismaili, K. Lolin, 2017, BMC Medical Genetics.

Outcome of Renal Transplantation in Eight Patients With Candida sp. Contamination of Preservation Fluid: Renal Transplantation With Preservation Fluid Contamination

K. Dahan, P. Grimbert, F. Botterel, 2008 .

Deletions of both α5(IV) and α6(IV) collagen genes in Alport syndrome and in Alport syndrome associated with smooth muscle tumours

C. Guyot, K. Dahan, K. Leppig, 1995 .

Mutation in the SLC2A9 Gene: A New Family with Familial Renal Hypouricemia Type 2

K. Dahan, Christian Maalouli, A. Devresse, 2021, Case reports in nephrology.

[Membranous nephropathy: Diagnosis, new insights in pathophysiology, and therapeutic approach].

K. Dahan, 2016, La Revue de medecine interne.

Factors Associated With Pathogenicity of Anti-Glomerular Basal Membrane Antibodies

K. Dahan, E. Rondeau, R. Tamouza, 2016, Medicine.

Severe parental phenotype associates with hypertension in children with ADPKD

K. Dahan, N. Demoulin, J. Morelle, 2023, Pediatric Nephrology.

ARSACS cause atypical and late-onset forms of SACS Mutations in

W. Robberecht, P. Bergh, K. Dahan, 2010 .

Constitutional microsatellite instability, genotype, and phenotype correlations in Constitutional Mismatch Repair Deficiency.

L. Guerrini-Rousseau, K. Dahan, G. Borthwick, 2022, Gastroenterology.

Laryngeal Signs of Ehlers Danlos Syndrome in an Adult

K. Dahan, Q. Gardiner, G. Desuter, 2009, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

High risk for neoplastic transformation of endometriosis in a carrier of lynch syndrome

C. Sempoux, K. Dahan, E. Marbaix, 2010, Familial Cancer.

Clinical and mutational spectrum of hypoparathyroidism, deafness and renal dysplasia syndrome

K. Dahan, Y. Pirson, V. Benoit, 2016, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

mTOR-activating mutations in RRAGD cause kidney tubulopathy and cardiomyopathy (KICA) syndrome

D. Sabatini, E. Schulze-Bahr, B. Schermer, 2021, bioRxiv.

Association of PKD2 (polycystin 2) mutations with left-right laterality defects.

K. Dahan, O. Devuyst, Y. Pirson, 2011, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Eculizumab in Anti-Factor H Antibodies Associated With Atypical Hemolytic Uremic Syndrome

K. Dahan, K. Ismaili, J. Davin, 2014, Pediatrics.

Survival and specific outcome of sickle cell disease patients after renal transplantation

K. Dahan, A. Moktefi, C. Couchoud, 2019, British journal of haematology.

Report of the Inefficacy of Eculizumab in Two Cases of Severe Antibody-Mediated Rejection of Renal Grafts

K. Dahan, C. Suberbielle, E. Rondeau, 2014, Transplantation.

Blau syndrome associated with a CARD15/NOD2 mutation.

K. Dahan, B. Snyers, 2006, American journal of ophthalmology.

Leg ulcers: a new symptom of Blau syndrome?

K. Dahan, H. Beele, V. Dhondt, 2008, European journal of dermatology : EJD.

Mild chronic renal failure with a family history of kidney disease

K. Dahan, O. Devuyst, Y. Pirson, 2009, NDT plus.

Smooth muscle tumors associated with X-linked Alport syndrome: carrier detection in females.

K. Dahan, K. Leppig, J. Zhou, 1995, Kidney international.

Frequent mutations of hepatocyte nuclear factor 1 in colorectal cancer with microsatellite instability.

J. Zucman‐Rossi, P. Laurent-Puig, K. Dahan, 2003, Gastroenterology.

Hepatitis B Virus Reactivation in Kidney Transplant Recipients Treated With Belatacept

K. Dahan, P. Grimbert, E. Rondeau, 2023, Kidney international reports.

Retreatment with rituximab for membranous nephropathy with persistently elevated titers of anti-phospholipase A2 receptor antibody.

K. Dahan, H. Debiec, P. Ronco, 2019, Kidney international.

Multiple Neoplasia in a 15-year-old Girl With Familial Adenomatous Polyposis

K. Dahan, C. Vermylen, C. Chantrain, 2009, Journal of pediatric hematology/oncology.

Late-onset renal failure in Senior-Loken syndrome.

K. Dahan, Y. Pirson, J. Cosyns, 2000, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Polymicrogyria in chromosome 22q11 deletion syndrome.

Stéphane Moniotte, Guillaume Sébire, Christine Verellen-Dumoulin, 2002, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Constitutional mismatch repair deficiency–associated brain tumors: report from the European C4CMMRD consortium

P. Varlet, F. Andreiuolo, L. Guerrini-Rousseau, 2019, Neuro-oncology advances.

Lessons for the clinical nephrologist: lumasiran as the future cornerstone treatment for patients with primary hyperoxaluria type 1?

K. Dahan, A. Devresse, A. Scohy, 2022, Journal of Nephrology.

Epidemiology, Outcomes, and Complement Gene Variants in Secondary Thrombotic Microangiopathies

K. Dahan, E. Levtchenko, C. Lambert, 2023, Clinical journal of the American Society of Nephrology : CJASN.

The authors reply.

J. Wetzels, K. Dahan, P. Ronco, 2018, Kidney international.

Identification of de novo deletion in the factor VIII gene by MLPA technique in two girls with isolated factor VIII deficiency

K. Dahan, C. Hermans, N. Lannoy, 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

Rituximab in Patients With Phospholipase A2 Receptor–Associated Membranous Nephropathy and Severe CKD

K. Dahan, J. Boffa, P. Fiévet, 2019, Kidney international reports.

Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21

M. Brown, K. Dahan, P. Danoy, 2010, Human Genetics.

Evidence of follicular T-cell implication in a case of IgG4-related systemic disease with interstitial nephritis.

P. Cervera-Pierot, K. Dahan, S. de Seigneux, 2011, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Follicular T cells and tissue IgG3 or IgG4 expressing plasma cells in a case of IgG4-related systemic disease with interstitial nephritis

P. Cervera-Pierot, K. Dahan, P. Callard, 2010 .

AUTOIMMUNE, CHOLESTATIC AND BILIARY DISEASE A Classification of Ductal Plate Malformations Based on Distinct Pathogenic Mechanisms of Biliary Dysmorphogenesis

C. Sempoux, P. Courtoy, K. Dahan, 2011 .

Serum Albumin Still of Interest to Predict Outcomes in Membranous Nephropathy in the Era of Phospholipase A2 Receptor

K. Dahan, N. Hanset, M. Delafosse, 2020, Kidney international reports.

Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease.

A. Need, M. Kayikci, M. Caulfield, 2023, Kidney international.

[Membranous nephropathy: New insights in therapeutic approach].

K. Dahan, K. Dahan, 2017, Nephrologie & therapeutique.

Paradoxical response to furosemide in uromodulin-associated kidney disease.

K. Dahan, O. Devuyst, Y. Pirson, 2015, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Phenotype and outcome in hereditary tubulointerstitial nephritis secondary to UMOD mutations.

K. Dahan, C. Antignac, D. Lacombe, 2011, Clinical journal of the American Society of Nephrology : CJASN.

Clinical trial recommendations for potential Alport syndrome therapies

Anne R. Pariser, C. Baigent, M. Prunotto, 2020, Kidney international.