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Lista de obras de Fabian Hauck

CD137 deficiency causes immune dysregulation with predisposition to lymphomagenesis

scientific article published on 01 October 2019

Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency).

artículo científico publicado en 2010

Complement C2 deficiency disarranging innate and adaptive humoral immune responses in a pediatric patient: Treatment with rituximab ⬇️

artículo científico publicado el 1 de marzo de 2011

DNA sensing via the cGAS/STING pathway activates the immunoproteasome and adaptive T‐cell immunity

artículo científico publicado en 2023

Disturbed B-lymphocyte selection in autoimmune lymphoproliferative syndrome

artículo científico publicado en 2016

Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency

artículo científico publicado en 2016

Heterozygous <i>OAS1</i> gain-of-function variants cause an autoinflammatory immunodeficiency

artículo científico publicado en 2021

Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy.

artículo científico publicado en 2018

IPEX due to an exon 7 skipping FOXP3 mutation with autoimmune diabetes mellitus cured by selective TReg cell engraftment

artículo científico publicado en 2018

Intestinal Inflammation and Dysregulated Immunity in Patients With Inherited Caspase-8 Deficiency

scientific article published on 26 September 2018

Outcomes for Nitazoxanide Treatment in a Case Series of Patients with Primary Immunodeficiencies and Rubella Virus-Associated Granuloma

artículo científico publicado en 2019

Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiency.

artículo científico publicado en 2012

SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling

artículo científico publicado en 2015

Somatic loss of heterozygosity, but not haploinsufficiency alone, leads to full-blown autoimmune lymphoproliferative syndrome in 1 of 12 family members with FAS start codon mutation

The Immune Deficiency and Dysregulation Activity (IDDA2.1 ‘Kaleidoscope’) Score and Other Clinical Measures in Inborn Errors of Immunity

artículo científico publicado en 2021

Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation

scientific article published on 21 March 2013

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