Yamina Hamel
Paris, 75015, France
Last Updated: 09/26/2026
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Found 15 publications
Identification of EPX Variants in Human Eosinophilic Granulomatosis With Polyangiitis (Churg-Strauss).
Journal: The journal of allergy and clinical immunology. In practice
Published: December 23, 2022
Compromised mitochondrial quality control triggers lipin1-related rhabdomyolysis.
Journal: Cell reports. Medicine
Published: April 01, 2020
Epithelial barrier dysfunction in desmoglein-1 deficiency.
Journal: The Journal of allergy and clinical immunology
Published: October 29, 2017
Cardiac function and exercise adaptation in 8 children with LPIN1 mutations.
Journal: Molecular genetics and metabolism
Published: September 30, 2017
Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal Encephalopathy.
Journal: American journal of human genetics
Published: March 28, 2017
Normal human adipose tissue functions and differentiation in patients with biallelic LPIN1 inactivating mutations.
Journal: Journal of lipid research
Published: February 02, 2017
Lack of interaction between NEMO and SHARPIN impairs linear ubiquitination and NF-κB activation and leads to incontinentia pigmenti.
Journal: The Journal of allergy and clinical immunology
Published: March 07, 2016
A unique CD8(+) T lymphocyte signature in pediatric type 1 diabetes.
Journal: Journal of autoimmunity
Published: October 20, 2015
IL36RN Mutations Affect Protein Expression and Function: A Basis for Genotype-Phenotype Correlation in Pustular Diseases.
Journal: The Journal of investigative dermatology
Published: May 31, 2015
Acute rhabdomyolysis and inflammation.
Journal: Journal of inherited metabolic disease
Published: December 01, 2014
Generation of Human Alloantigen-Specific Regulatory T Cells Under Good Manufacturing Practice-Compliant Conditions for Cell Therapy.
Journal: Cell transplantation
Published: September 09, 2014
Last Updated: 09/26/2026