Capucine A. Picard

EA 7379 EpiDermE, Université Paris Est
Creteil, France

Last Updated: 09/26/2026

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Found 347 publications

Eczema in inborn errors of immunity with atopy: frequency, timing, phenotypic clustering.

Eczema in inborn errors of immunity with atopy: frequency, timing, phenotypic clustering.

Journal: The British journal of dermatology

Published: May 14, 2026

Paediatric-onset autoimmune cytopenia: How can we reduce the long-term mortality?

Paediatric-onset autoimmune cytopenia: How can we reduce the long-term mortality?

Journal: British journal of haematology

Published: March 11, 2026

FOXP3 deep intronic variant underlying IPEX.

FOXP3 deep intronic variant underlying IPEX.

Journal: Journal of human immunity

Published: February 14, 2026

Fast and compact scatterometer for ex vivo qualification of low-scattering biological samples.

Fast and compact scatterometer for ex vivo qualification of low-scattering biological samples.

Journal: The Review of scientific instruments

Published: February 11, 2026

Cryptosporidiosis in Ptients with Inborn Errors of Immunity: Retrospective cohort study of the French National Reference Center (CEREDIH).

Cryptosporidiosis in Ptients with Inborn Errors of Immunity: Retrospective cohort study of the French National Reference Center (CEREDIH).

Journal: The Journal of infectious diseases

Published: January 21, 2026

Intronic branchpoint-to-acceptor variants underlying inborn errors of immunity.

Intronic branchpoint-to-acceptor variants underlying inborn errors of immunity.

Journal: Journal of human immunity

Published: December 15, 2025

Exome sequencing enables molecular diagnosis in 10% of early-onset or familial systemic lupus erythematosus cases.

Exome sequencing enables molecular diagnosis in 10% of early-onset or familial systemic lupus erythematosus cases.

Journal: EBioMedicine

Published: October 07, 2025

An unusual case of RIPK1-related immunodeficiency: The importance of a timely diagnosis for a novel clinical and therapeutic pattern.

An unusual case of RIPK1-related immunodeficiency: The importance of a timely diagnosis for a novel clinical and therapeutic pattern.

Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology

Published: October 01, 2025

Expanding the clinical spectrum of RNU4ATAC-opathies: More frequent and diverse than assumed.

Expanding the clinical spectrum of RNU4ATAC-opathies: More frequent and diverse than assumed.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: October 01, 2025

Expanding the clinical spectrum of RNU4ATAC-opathies: more frequent and diverse than assumed.

Expanding the clinical spectrum of RNU4ATAC-opathies: more frequent and diverse than assumed.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: October 01, 2025

Characterization of Streptococcus pyogenes isolates from French children: emm-1 genotype is associated with invasive infections and spread of the M1UK clone.

Characterization of Streptococcus pyogenes isolates from French children: emm-1 genotype is associated with invasive infections and spread of the M1UK clone.

Journal: Journal of the Pediatric Infectious Diseases Society

Published: September 01, 2025

Childhood isolated C3d-positive AIHA: favorable prognosis but rare relapse or associated immunodeficiency.

Childhood isolated C3d-positive AIHA: favorable prognosis but rare relapse or associated immunodeficiency.

Journal: Blood advances

Published: June 02, 2025

Showing 1-12 of 347

Last Updated: 09/26/2026