Late-onset hemophagocytic lymphohistiocytosis with neurological presentation

Author:

Benezech Sarah1ORCID,Walzer Thierry2,Charrier Emily2,Heidelberg Damien3,De Saint-Basile Geneviève4,Bertrand Yves5,Belot Alexandre26

Affiliation:

1. Department of Pediatrics; Hospices Civils de Lyon; Lyon France

2. Institut National de la Santé et de la Recherche Médicale U1111; Université de Lyon 1; Lyon France

3. Department of Radiology; Hospices Civils de Lyon; Lyon France

4. Institut National de la Santé et de la Recherche Médicale U768; CHU Paris - Hôpital Necker-Enfants Malades; Paris France

5. Hospices Civils de Lyon; Institut d'Hématologie et Oncologie Pédiatrique; Lyon France

6. Department of Rheumatology; Hospices Civils de Lyon; Lyon France

Publisher

Wiley

Subject

General Medicine

Reference57 articles.

1. Pillars article: Perforin gene defects in familial hemophagocytic lymphohistiocytosis. Science. 1999. 286: 1957-1959;Stepp;J. Immunol.,2015

2. HLH-2004: diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis;Henter;Pediatr. Blood Cancer,2007

3. Analysis of protein-coding genetic variation in 60,706 humans;Lek;Nature,2016

4. Treatment of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins, steroids, and cyclosporin A;Stéphan;Blood,1993

5. Familial hemophagocytic lymphohistiocytosis: when rare diseases shed light on immune system functioning;Sieni;Front Immunol.,2014

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