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Centre de Référence Déficits Immunitaires Héréditaires | Researchclopedia

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Centre de Référence Déficits Immunitaires Héréditaires

Parisfacility

983

Works

138,163

Citations

192

h-index

Top Research Topics

Immunodeficiency and Autoimmune Disorders Hearing, Cochlea, Tinnitus, Genetics Immune Cell Function and Interaction

Top Researchers

Jean‐Laurent Casanova Uppsala University

1,394 works119,012 citationsh-index: 171

Recent Research

Homozygosity for rare or common hypomorphic <i>IL23R</i> variants confers a predisposition to tuberculosis in humans

Damelys Calderon,Laura E. Kilpatrick,et al.

20260 citations

Blood disorders and treatments

Academic Research in Diverse Fields

Connexins and lens biology

Vestibular and auditory disorders

Autoimmune and Inflammatory Disorders Research

Cystic Fibrosis Research Advances

Pneumocystis jirovecii pneumonia detection and treatment

T-cell and B-cell Immunology

Neutrophil, Myeloperoxidase and Oxidative Mechanisms

Jean Weissenbach Centre National de la Recherche Scientifique

253 works107,491 citationsh-index: 99

1,208 works101,430 citationsh-index: 157

Wolf H. Fridman The University of Texas MD Anderson Cancer Center

1,044 works87,850 citationsh-index: 120

Christopher Gillberg University of Gothenburg

1,030 works75,003 citationsh-index: 138

Vincent Michel Inserm

107 works70,379 citationsh-index: 39

Incidental maternal glutaric aciduria type I detection through newborn screening: A case report

Pierre-Edouard Grillet,Cecilia Marelli,et al.

20260 citations

La maladie de Whipple, entre génétique et environnement, à propos de deux frères

B. Bourdon,M. Hardelin,et al.

20250 citations

Caractérisation de l’eczéma dans les erreurs innées de l’immunité avec atopie : prévalence, chronologie et description phénotypique

H. Aubert,Mickaël Alligon,et al.

20250 citations

#3363 Diagnostic gaps in C3G and ic-MPGN: findings of the CompCure study cohort

Giulia Bassanese,Joanna Śladowska-Kozłowska,et al.

20250 citations

Novel de novo dominant <i>PSMB10</i> variants in three patients with immune deficiency and liver disease

Benjamin Fournier,Léa Poirier,et al.

20251 citations