Résultat de recherche

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

Frédéric Rieux-Laucat

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RAS-associated lymphoproliferative disease evolves into severe juvenile myelo-monocytic leukemia.

Frédéric Rieux-Laucat

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Defective anti-polysaccharide response and splenic marginal zone disorganization in ALPS patients.

Frédéric Rieux-Laucat

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Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations.

Frédéric Rieux-Laucat

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LRBA deficiency with autoimmunity and early onset chronic erosive polyarthritis.

Frédéric Rieux-Laucat

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Efficacy of the Janus kinase 1/2 inhibitor ruxolitinib in the treatment of vasculopathy associated with TMEM173-activating mutations in 3 children

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Evolution of disease activity and biomarkers on and off rapamycin in 28 patients with autoimmune lymphoproliferative syndrome.

Bénédicte Neven

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

Frédéric Rieux-Laucat

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What's up in the ALPS.

Frédéric Rieux-Laucat

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Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations.

Frédéric Rieux-Laucat

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Autoimmune Lymphoproliferative Syndrome-FAS Patients Have an Abnormal Regulatory T Cell (Treg) Phenotype but Display Normal Natural Treg-Suppressive Function on T Cell Proliferation.

Frédéric Rieux-Laucat

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