Résultat de recherche

Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a...

Autoimmune lymphoproliferative syndrome with somatic Fas mutations.

Mutations in Fas associated with human lymphoproliferative syndrome and...

Inactivation of the Fas gene by Alu insertion: retrotransposition in an...

Inherited and somatic CD3zeta mutations in a patient with T-cell defic...

FAS-L, IL-10, and double-negative CD4- CD8- TCR alpha/beta+ T cells are...

Reduced expression of FOXP3 and regulatory T-cell function in severe forms...

A survey of 90 patients with autoimmune lymphoproliferative syndrome related...

Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS...

New Publication

Diagnosis of autoimmune lymphoproliferative syndrome caused by FAS deficiency...

RAS-associated lymphoproliferative disease evolves into severe juvenile...

Defective anti-polysaccharide response and splenic marginal zone disorganization...

Inherited STING-activating mutation underlies a familial inflammatory syndrome...

LRBA deficiency with autoimmunity and early onset chronic erosive poly...

Efficacy of the Janus kinase 1/2 inhibitor ruxolitinib in the treatment...

Evolution of disease activity and biomarkers on and off rapamycin in 28...

Intrinsic antiproliferative activity of the innate sensor STING in T l...

What's up in the ALPS.

Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency...