UNSMAKING PRIMARY IMMUNE DEFICIENCIES IN EARLY-ONSET EVANS SYNDROME ă USING IMMUNOPHENOTYPING AND NGS: TOWARDS A CLINICAL AND GENETIC ă CLASSIFICATION

0 avis

UNSMAKING PRIMARY IMMUNE DEFICIENCIES IN EARLY-ONSET EVANS SYNDROME ă USING IMMUNOPHENOTYPING AND NGS: TOWARDS A CLINICAL AND GENETIC ă CLASSIFICATION

Archive ouverte

Edité par CCSD ; Ferrata Storti Foundation -

21st Congress of the European-Hematology-Association, Copenhagen, ă DENMARK, JUN 09-12, 2016. International audience. no abstract

Langue: en

Indexation

Consulter en ligne

Consulter le document

Suggestions

Du même auteur

Second-line treatment trends and long-term outcomes of 392 children with chronic immune thrombocytopenic purpura: the French experience over the past 25 years. : Br J Haematol

Archive ouverte | Ducassou, S. | CCSD

International audience. Childhood chronic immune thrombocytopenic purpura (cITP) is a rare disease. In severe cases, there is no evidence for the optimal therapeutic strategy. Our aim was to describe the real‐life m...

Monogenic Early-Onset Lymphoproliferation and Autoimmunity: The Natural History of STAT3 GOF Syndrome.

Archive ouverte | Leiding, J. W. | CCSD

International audience. BackgroundIn 2014, germline signal transducer and activator of transcription (STAT) 3 gain-of-function (GOF) mutations were first described to cause a novel multisystem disease of early-onset...

POS0378 HETEROZYGOUS LOSS-OF-FUNCTION RELA MUTATIONS LEAD TO SYSTEMIC LUPUS ERYTHEMATOSUS OR AUTOINFLAMMATORY SYNDROME

Archive ouverte | Riller, Q. | CCSD

International audience

Chargement des enrichissements...