Marianne Debré

Immunology and Microbiology · Life Sciences

39h-index7.1kcitations102works0.02yr avg
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Research Topics

Immunodeficiency and Autoimmune Disorders(40), Blood disorders and treatments(12), Immune Cell Function and Interaction(9), Chronic Lymphocytic Leukemia Research(8), HIV-related health complications and treatments(8)

Publications100 total

Adaptation and Coping of HIV Infected Adolescents Living in France
2022
Correction to: A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary Immunodeficiency
Journal of Clinical Immunology·2020· 1 citedOpen Access
A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary Immunodeficiency
Journal of Clinical Immunology·2019· 8 cited
FRI0509 Chromosome 22Q11.2 Deletion Syndrome (Digeorge Syndrome) and Autoimmunity: A French Retrospective Pediatric Study of 15 Cases
Annals of the Rheumatic Diseases·2015
Immune deficiency–related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency
Journal of Allergy and Clinical Immunology·2014· 82 cited
Inflammatory manifestations in a single-center cohort of patients with chronic granulomatous disease
Journal of Allergy and Clinical Immunology·2014· 164 citedOpen Access
SFP CO-03 - Syndrome de Di George et manifestations auto immunes, à propos de 15 cas
Archives de Pédiatrie·2014
Occurrence of B-cell lymphomas in patients with activated phosphoinositide 3-kinase δ syndrome
Journal of Allergy and Clinical Immunology·2014· 108 citedOpen Access
Live rubella virus vaccine long-term persistence as an antigenic trigger of cutaneous granulomas in patients with primary immunodeficiency
Clinical Microbiology and Infection·2014· 89 citedOpen Access
Phosphoinositide 3-Kinase δ Gene Mutation Predisposes to Respiratory Infection and Airway Damage
Science·2013· 609 citedOpen Access
UTILISATION DES IMMUNOGLOBULINES HUMAINES CHEZ L'ENFANT
Maroc médical·2013· 1 citedOpen Access
Polymerase ε1 mutation in a human syndrome with facial dysmorphism, immunodeficiency, livedo, and short stature (“FILS syndrome”)
The Journal of Experimental Medicine·2012· 98 citedOpen Access
Prise en charge thérapeutique des granulomes cutanés chez 11 enfants suivis pour déficit immunitaire primitif
Annales de Dermatologie et de Vénéréologie·2012
Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency
Nature Immunology·2012· 461 citedOpen Access
Inherited MST1 Deficiency Underlies Susceptibility to EV-HPV Infections
PLoS ONE·2012· 143 citedOpen Access
Prevalence and Clinical Impact of Norovirus Fecal Shedding in Children with Inherited Immune Deficiencies
The Journal of Infectious Diseases·2012· 81 citedOpen Access
Autosomal Dominant STAT3 Deficiency and Hyper-IgE Syndrome
Medicine·2012· 323 citedOpen Access
Protective effect of IgM against colonization of the respiratory tract by nontypeable Haemophilus influenzae in patients with hypogammaglobulinemia
Journal of Allergy and Clinical Immunology·2011· 47 citedOpen Access
Invasive Mold Infections in Chronic Granulomatous Disease: A 25-Year Retrospective Survey
Clinical Infectious Diseases·2011· 135 citedOpen Access
Cataract surgery with primary intraocular lens implantation in children with uveitis: Long-term outcomes
Journal of Cataract & Refractive Surgery·2011· 48 cited
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Frequent Co-authors

Alain Fischer(28), Capucine Pïcard(17), Stéphane Blanche(15), Jean‐Laurent Casanova(11), Anne Durandy(9), C Griscelli(9), Nizar Mahlaoui(9), Geneviève de Saint Basile(9), Olivier Hermine(8), Frédéric Rieux‐Laucat(6), Pierre Quartier(6), Caroline Thomas(6), Felipe Suárez(6), Bénédicte Neven(6), Françoise Le Deist(6), Diana M. Gibb(6), Isabelle Pellier(5), Julien Beauté(5), Marina Cavazzana(4), Brigitte Bader‐Meunier(4)