Primary necrotizing lymphocytic central nervous system vasculitis due to perforin deficiency in a four-year-old girl-Reference-Cited by-同舟云学术

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Primary necrotizing lymphocytic central nervous system vasculitis due to perforin deficiency in a four-year-old girl

Published:2007 Issue:3 Volume:56 Page:995-999
ISSN:0004-3591
Container-title:Arthritis & Rheumatism
language:en
Short-container-title:Arthritis Rheum

Author:

Moshous Despina,Feyen Oliver,Lankisch Petra,Schwarz Klaus,Schaper Jörg,Schneider Marion,Dilloo Dagmar,Laws Hans-Jürgen,Schwahn Bernd C.,Niehues Tim

Publisher

Wiley

Subject

Pharmacology (medical),Immunology,Rheumatology,Immunology and Allergy

Reference19 articles.

1. Central nervous system vasculitis in children

2. Perforin Gene Defects in Familial Hemophagocytic Lymphohistiocytosis

3. Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses ofPRF1, UNC13D, STX11, andRAB27A

4. Behandlung der Hämophagozytischen Lymphohistiozytose, HLH, mit Knochenmarktransplantation

Cited by 52 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Case Report: Chronic inflammatory demyelinating polyradiculoneuropathy rather than hemophagocytic lymphohistiocytosis—the initial phenotype of PRF1 gene mutation;Frontiers in Immunology;2023-12-11

2. Familial hemophagocytic phohistiocytosis induced by PRF1 mutation with neurologic manifestations as the initial clinical presentations: A case report;Medicine;2023-06-30

3. Primary Hemophagocytic Lymphohistiocytosis With Prolonged Primary Neurologic Presentation;Pediatrics;2023-03-24

4. Child Neurology: Familial Hemophagocytic Lymphohistiocytosis Underlying Isolated CNS Inflammation;Neurology;2022-08-10

5. Treatment Strategies for Central Nervous System Effects in Primary and Secondary Haemophagocytic Lymphohistiocytosis in Children;Current Treatment Options in Neurology;2022-02

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