J. Feinberg

发表

Low Penetrance, Broad Resistance, and Favorable Outcome of Interleukin 12 Receptor β1 Deficiency

Sami Al-Hajjar, A. Fischer, J. Casanova, 2003, The Journal of Experimental Medicine.

Low penetrance, broad resistance, and favorable outcome of interleukin 12 receptor beta1 deficiency: medical and immunological implications.

Sami Al-Hajjar, A. Fischer, J. Casanova, 2003, The Journal of experimental medicine.

Bacillus Calmette Guérin triggers the IL‐12/IFN‐γ axis by an IRAK‐4‐ and NEMO‐dependent, non‐cognate interaction between monocytes, NK, and T lymphocytes

J. Casanova, C. Picard, M. Feinberg, 2004, European journal of immunology.

Gains of glycosylation comprise an unexpectedly large group of pathogenic mutations

Guillaume Vogt, David N Cooper, Mehdi Mirsaeidi, 2005, Nature Genetics.

In vitro and in vivo activity of sacituzumab govitecan, an antibody-drug conjugate targeting trophoblast cell-surface antigen 2 (Trop-2) in uterine serous carcinoma.

Gloria S. Huang, E. Ratner, D. Silasi, 2019, Gynecologic Oncology.

« Les mutations "gain de glycosylation" / Gains of glycosylation mutations »

D. Cooper, N. Chuzhanova, L. Abel, 2015 .

CD56+ T cells in vivo A role for interleukin-12/23 in the maturation of human natural killer and

Sami Al-Hajjar, J. Casanova, L. Abel, 2013 .

o Mycobacterial Disease in Egyptian Children

J. Bustamante, S. Boisson-Dupuis, J. Feinberg, 2012 .

Mendelian Susceptibility to Mycobacterial Disease in Egyptian Children

J. Casanova, J. Bustamante, S. Boisson-Dupuis, 2012, Mediterranean journal of hematology and infectious diseases.

Mendelian Susceptibility to Mycobacterial Disease in Egyptian Children

J. Casanova, J. Bustamante, S. Boisson-Dupuis, 2012, Mediterranean journal of hematology and infectious diseases.

Bacille Calmette-Guérin Lymphadenitis and Recurrent Oral Candidiasis in an Infant With a New Mutation Leading to Interleukin-12 Receptor ß-1 Defi ciency

J. Casanova, J. Casanova, J. Bustamante, 2011 .

Disseminated Mycobacterium scrofulaceum infection in a child with interferon-gamma receptor 1 deficiency.

J. Casanova, V. Pistoia, A. Chapgier, 2010, International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases.

A novel form of cell type-specific partial IFN-gammaR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon.

J. Casanova, L. Abel, A. Puel, 2010, Human molecular genetics.

A role for interleukin-12/23 in the maturation of human natural killer and CD56+ T cells in vivo.

Sami Al-Hajjar, J. Casanova, L. Abel, 2008, Blood.

Mycobacterial disease in a child with surface-expressed non-functional interleukin-12Rbeta1 chains.

J. Casanova, B. Garty, J. Feinberg, 2007, The Israel Medical Association journal : IMAJ.

Disseminated Mycobacterium avium Infection in a 20-Year-Old Female with Partial Recessive IFNγR1 Deficiency

J. Casanova, A. Chapgier, J. Feinberg, 2006, Respiration.

Les mutations « gain de glycosylation »

J. Casanova, D. Cooper, N. Chuzhanova, 2006 .

Analysis of the interleukin-12/interferon-γ pathway in children with non-tuberculous mycobacterial cervical lymphadenitis

J. Casanova, C. Picard, I. Dalal, 2007, European Journal of Pediatrics.

Interleukin-12 receptor beta 1 chain deficiency in a child with disseminated tuberculosis.

J. Casanova, C. Fieschi, J. Feinberg, 2005, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Evaluating the Impact of a New Smartphone Texting Tool on Patient Care in Obstetrics, an Emergent Healthcare Setting

J. Illuzzi, C. Pettker, J. Feinberg, 2019, Applied Clinical Informatics.

Robotic Surgery in the Frail Elderly: Analysis of Perioperative Outcomes

Carol L. Brown, D. Chi, G. Gardner, 2020, Annals of Surgical Oncology.

Is Robotic-Assisted Surgery Safe in the Elderly Population? An Analysis of Gynecologic Procedures in Patients ≥ 65 Years Old

Carol L. Brown, R. Barakat, G. Gardner, 2018, Annals of Surgical Oncology.

Ten-Year Comparison Study of Type 1 and 2 Endometrial Cancers: Risk Factors and Outcomes

E. Ratner, D. Silasi, P. Schwartz, 2019, Gynecologic and Obstetric Investigation.

Crucial function of the pre‐T‐cell receptor (TCR) in TCRP selection, TCRβ allelic exclusion and αβ versus γδ lineage commitment

J. Buer, I. Aifantis, C. Saint‐Ruf, 1998, Immunological reviews.

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.

New developments in the treatment of Pneumocystis carinii pneumonia.

J. Feinberg, J. Feinberg, F. Sattler, 1992, Chest.

Impaired interferon‐γ production in response to live bacteria and Toll‐like receptor agonists in patients with ataxia telangiectasia

M. Rose, R. Schubert, S. Zielen, 2006 .

BCG-osis and tuberculosis in a child with chronic granulomatous disease.

J. Casanova, J. Emile, A. Chapgier, 2007, The Journal of allergy and clinical immunology.

Inherited IL-12p40 Deficiency: Genetic, Immunologic, and Clinical Features of 49 Patients From 30 Kindreds (vol 92, pg 109, 2013)

Sami Al-Hajjar, C. Picard, L. Abel, 2013 .

Mutations in STAT3 and IL12RB1 impair the development of human IL-17–producing T cells

A. Fischer, J. Casanova, C. Picard, 2008, The Journal of experimental medicine.

The Common Cytokine Receptor γ Chain and the Pre-T Cell Receptor Provide Independent but Critically Overlapping Signals in Early α/β T Cell Development

A. Fischer, H. Fehling, J. D. Di Santo, 1999, The Journal of experimental medicine.

Allelic Exclusion of the T Cell Receptor β Locus Requires the Sh2 Domain–Containing Leukocyte Protein (Slp)-76 Adaptor Protein

F. Alt, R. Geha, W. Swat, 1999, The Journal of experimental medicine.

Genomic structure of the human pre‐T cell receptor α chain and expression of two mRNA isoforms

C. Saint‐Ruf, H. von Boehmer, O. Lechner, 1998 .

Genomic structure of the human pre-T cell receptor alpha chain and expression of two mRNA isoforms.

C. Saint‐Ruf, H. von Boehmer, O. Lechner, 1998, European journal of immunology.

Hodgkin lymphoma in 2 children with chronic granulomatous disease.

A. Fischer, J. Casanova, C. Picard, 2011, The Journal of allergy and clinical immunology.

Current and novel mapping substances in gynecologic cancer care

E. J. Levy, J. Feinberg, L. Moukarzel, 2020, International Journal of Gynecological Cancer.

The prevalence of occult leiomyosarcoma at surgery for presumed uterine fibroids: a meta-analysis

J. Berek, D. Vanness, D. Olive, 2015, Gynecological Surgery.

Early T Cell Receptor β Gene Expression Is Regulated by the Pre-T Cell Receptor–CD3 Complex

H. Fehling, J. D. Di Santo, I. Aifantis, 1999, The Journal of experimental medicine.

On the Role of the Pre–T Cell Receptor in αβ versus γδ T Lineage Commitment

J. Buer, I. Aifantis, C. Saint‐Ruf, 1998 .

527 Low Penetrance, Broad Resistance, and Favorable Outcome of Interleukin 12 Receptor (cid:2) 1 Deﬁciency: Medical and Immunological

Sami Al-Hajjar, F. Deist, J. Casanova, 2003 .

Inborn errors of IL-12/23- and IFN-gamma-mediated immunity: molecular, cellular, and clinical features.

J. Casanova, C. Picard, E. Jouanguy, 2006, Seminars in immunology.

A novel form of complete IL-12/IL-23 receptor (cid:1) 1 deﬁciency with cell surface–expressed nonfunctional receptors

J. Casanova, F. Candotti, M. Bosticardo, 2004 .

Management of sexuality, intimacy, and menopause symptoms in patients with ovarian cancer

E. Ratner, J. Black, G. Menderes, 2017, American journal of obstetrics and gynecology.

Trimetrexate-leucovorin dosage evaluation study for treatment of Pneumocystis carinii pneumonia.

J. Shelhamer, H. Lane, C. Allegra, 1990, The Journal of infectious diseases.

Revisiting Human IL-12R&bgr;1 Deficiency: A Survey of 141 Patients From 30 Countries

Smita Y. Patel, A. Al-ghonaium, Sami Al-Hajjar, 2010, Medicine.

Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease

J. Casanova, P. Newburger, C. Picard, 2011, Nature Immunology.

A novel X-linked recessive form of Mendelian susceptibility to mycobaterial disease

J. Casanova, C. Picard, A. Lemainque, 2006, Journal of Medical Genetics.

Inborn errors of IL-12/23- and IFN-γ-mediated immunity: molecular, cellular, and clinical features

J. Casanova, C. Picard, E. Jouanguy, 2006 .

Partial recessive IFN-γR1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindreds.

J. Casanova, C. Picard, S. Holland, 2011, Human molecular genetics.

Brief Definitive Report

J. Casanova, C. Picard, J. Puck, 2003 .

Pyogenic Bacterial Infections in Humans with IRAK-4 Deficiency

A. Al-ghonaium, Sami Al-Hajjar, S. Al-Jumaah, 2003, Science.

A partial form of recessive STAT1 deficiency in humans.

J. Casanova, Shen-Ying Zhang, L. Abel, 2009, The Journal of clinical investigation.

IRF8 mutations and human dendritic-cell immunodeficiency.

Damien Chaussabel, Xiao-Fei Kong, Florent Ginhoux, 2011, The New England journal of medicine.

Novel targeted therapies in ovarian and uterine carcinosarcomas.

A. Santin, G. Menderes, S. Lopez, 2018, Discovery medicine.

Accounting for genetic heterogeneity in homozygosity mapping: application to Mendelian susceptibility to mycobacterial disease

J. Casanova, O. Sanal, A. Boland, 2011, Journal of Medical Genetics.

Pleiotropic changes controlled by the pre-T-cell receptor.

J. Buer, I. Aifantis, C. Saint‐Ruf, 1999, Current opinion in immunology.

Paternal uniparental isodisomy of chromosome 6 causing a complex syndrome including complete IFN‐γ receptor 1 deficiency

J. Casanova, L. Abel, S. Lyonnet, 2010, American journal of medical genetics. Part A.

IL-12Rβ1 Deficiency in Two of Fifty Children with Severe Tuberculosis from Iran, Morocco, and Turkey

J. Casanova, A. Bousfiha, L. Abel, 2011, PloS one.

An eQTL variant of ZXDC is associated with IFN-γ production following Mycobacterium tuberculosis antigen-specific stimulation

C. Delacourt, J. Casanova, C. Deswarte, 2017, Scientific Reports.

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.

Inherited interleukin-12 deficiency: IL12B genotype and clinical phenotype of 13 patients from six kindreds.

A. Al-ghonaium, Sami Al-Hajjar, J. Casanova, 2002, American journal of human genetics.

A novel form of human STAT1 deficiency impairing early but not late responses to interferons.

Sami Al-Hajjar, D. Chaussabel, J. Casanova, 2010, Blood.

A Novel Approach to Combined Vaginal and Laparoscopic Gynecological Surgery

G. Menderes, J. Feinberg, M. Azodi, 2019, JSLS : Journal of the Society of Laparoendoscopic Surgeons.

Clindamycin and primaquine as primary treatment for mild and moderately severePneumocystis carinii pneumonia in patients with AIDS

R. Murphy, J. Feinberg, R. Fass, 1991, European Journal of Clinical Microbiology and Infectious Diseases.

Recurrent non-typhoidal salmonella bacteremia in a patient with interleukin -12p40 deficiency.

J. Casanova, M. Mohraz, M. Naderi, 2004, Iranian journal of allergy, asthma, and immunology.

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.

Human Complete Stat-1 Deficiency Is Associated with Defective Type I and II IFN Responses In Vitro but Immunity to Some Low Virulence Viruses In Vivo1

J. Casanova, Shen-Ying Zhang, E. Jouanguy, 2006, The Journal of Immunology.

The NEMO mutation creating the most-upstream premature stop codon is hypomorphic because of a reinitiation of translation.

A. Smahi, R. Döffinger, J. Casanova, 2006, American journal of human genetics.

A novel form of complete IL-12/IL-23 receptor beta1 deficiency with cell surface-expressed nonfunctional receptors.

J. Casanova, F. Candotti, M. Bosticardo, 2004, Blood.

Novel STAT1 Alleles in Otherwise Healthy Patients with Mycobacterial Disease

J. Casanova, R. Schreiber, C. Picard, 2006, PLoS genetics.

Inherited IL-12p40 Deficiency

Sami Al-Hajjar, J. Casanova, C. Picard, 2013, Medicine.

Successful hematopoietic stem cell transplantation from an unrelated donor in a child with interferon gamma receptor deficiency.

J. Casanova, A. Chapgier, M. Arola, 2009, The Pediatric infectious disease journal.

CorrigendumCorrigendum to “Inborn errors of IL-12/23- and IFN-γ-mediated immunity: Molecular, cellular, and clinical features” [Semin. Immunol. 18 (2006) 347–361]

J. Casanova, C. Picard, E. Jouanguy, 2007 .

Immunologic aspects of patients with disseminated bacille Calmette-Guerin disease in north-west of Iran

J. Casanova, K. Ansarin, J. de Villartay, 2009, Italian journal of pediatrics.

A Review of Immune Checkpoint Blockade Therapy in Endometrial Cancer.

A. Green, J. Feinberg, V. Makker, 2020, American Society of Clinical Oncology educational book. American Society of Clinical Oncology. Annual Meeting.

Clindamycin and primaquine therapy for mild-to-moderate episodes of Pneumocystis carinii pneumonia in patients with AIDS: AIDS Clinical Trials Group 044.

D. Finkelstein, R. Murphy, J. Plouffe, 1994, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

On the role of the pre-T cell receptor in alphabeta versus gammadelta T lineage commitment.

J. Buer, I. Aifantis, C. Saint‐Ruf, 1998, Immunity.

Major Loci on Chromosomes 8q and 3q Control Interferon γ Production Triggered by Bacillus Calmette-Guerin and 6-kDa Early Secretory Antigen Target, Respectively, in Various Populations

C. Delacourt, J. Casanova, L. Abel, 2015, The Journal of infectious diseases.

Association of IL12RB1 polymorphisms with pulmonary tuberculosis in adults in Morocco.

J. Casanova, L. Abel, N. Remus, 2004, The Journal of infectious diseases.

In Vitro and In Vivo Activity of IMGN853, an Antibody–Drug Conjugate Targeting Folate Receptor Alpha Linked to DM4, in Biologically Aggressive Endometrial Cancers

Gloria S. Huang, E. Ratner, Serena Wong, 2018, Molecular Cancer Therapeutics.

Inherited disorders of the IL-12-IFN-γ axis in patients with disseminated BCG infection

J. Casanova, A. Velayati, M. Mirsaeidi, 2005, European Journal of Pediatrics.

Inherited disorders of the IL-12-IFN-gamma axis in patients with disseminated BCG infection.

J. Casanova, A. Velayati, M. Mirsaeidi, 2005, European journal of pediatrics.

Impaired interferon-gamma production in response to live bacteria and Toll-like receptor agonists in patients with ataxia telangiectasia.

M. Rose, R. Schubert, S. Zielen, 2006, Clinical and experimental immunology.

Aerosolized pentamidine and Pneumocystis carinii pneumonia.

P. Hopewell, J. Mills, J. Luce, 1989, Annals of internal medicine.

Complementation of a pathogenic IFNGR 2 misfolding mutation with modifi ers of N-glycosylation

J. Casanova, C. Picard, J. Puck, 2008 .

Simultaneous presentation of 2 rare hereditary immunodeficiencies: IL-12 receptor beta1 deficiency and ataxia-telangiectasia.

J. Casanova, R. Gatti, S. Nahas, 2008, The Journal of allergy and clinical immunology.

Complete deficiency of the IL-12 receptor β1 chain: three unrelated Turkish children with unusual clinical features

J. Casanova, A. Ikinciogullari, C. Aytekin, 2006, European Journal of Pediatrics.

The use of QuikClot combat gauze in cervical and vaginal hemorrhage

E. Ratner, J. Black, J. Feinberg, 2017, Gynecologic oncology reports.

Disseminated Mycobacterium avium infection in a 20-year-old female with partial recessive IFNgammaR1 deficiency.

J. Casanova, A. Chapgier, J. Feinberg, 2006, Respiration; international review of thoracic diseases.

BCG Lymphadenitis and Recurrent Oral Candidiasis in an Infant with a New Mutation Leading to Interleukin-12 Receptor Beta-1 Deficiency

J. Casanova, S. Boisson-Dupuis, A. Ikinciogullari, 2011 .

Complementation of a pathogenic IFNGR2 misfolding mutation with modifiers of N-glycosylation

J. Casanova, C. Picard, J. Puck, 2008, The Journal of experimental medicine.

Partial recessive IFN-γR1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindreds.

J. Casanova, C. Picard, S. Holland, 2011, Human molecular genetics.

Revisiting Human IL-12R&bgr;1 Deficiency: A Survey of 141 Patients From 30 Countries

Smita Y. Patel, A. Al-ghonaium, Sami Al-Hajjar, 2010, Medicine.

The Common Cytokine Receptor γ Chain and the Pre-T Cell Receptor Provide Independent but Critically Overlapping Signals in Early α/β T Cell Development

A. Fischer, H. Fehling, J. D. Di Santo, 1999, The Journal of experimental medicine.

A role for interleukin-12/23 in the maturation of human natural killer and CD56+ T cells in vivo.

Sami Al-Hajjar, J. Casanova, L. Abel, 2008, Blood.

Major Loci on Chromosomes 8q and 3q Control Interferon γ Production Triggered by Bacillus Calmette-Guerin and 6-kDa Early Secretory Antigen Target, Respectively, in Various Populations

L. Abel, A. Alcaïs, S. Boisson-Dupuis, 2015, The Journal of infectious diseases.

Mendelian Susceptibility to Mycobacterial Disease in Egyptian Children

J. Casanova, S. Boisson-Dupuis, J. Feinberg, 2012, Mediterranean journal of hematology and infectious diseases.

Early T Cell Receptor β Gene Expression Is Regulated by the Pre-T Cell Receptor–CD3 Complex

H. Fehling, J. D. Di Santo, I. Aifantis, 1999, Journal of Experimental Medicine.

Complementation of a pathogenic IFNGR2 misfolding mutation with modifiers of N-glycosylation

J. Puck, N. Mahlaoui, A. Alcaïs, 2008, The Journal of experimental medicine.