A teenage boy with late onset hemophagocytic lymphohistiocytosis with predominant neurologic disease and perforin deficiency-Reference-Cited by-同舟云学术

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A teenage boy with late onset hemophagocytic lymphohistiocytosis with predominant neurologic disease and perforin deficiency

Published:2008 Issue:5 Volume:50 Page:1070-1072
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr. Blood Cancer

Author:

Beaty Andrew D.,Weller Christin,Levy Beth,Vogler Carole,Ferguson William S.,Bicknese Alma,Knutsen Alan P.

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Reference20 articles.

1. HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis

2. Hemophagocytic lymphohistiocytosis and related disorders

3. FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS

4. An inframe perforin gene deletion in familial hemophagocytic lymphohistiocytosis is associated with perforin expression

5. A null mutation in the perforin gene impairs cytolytic T lymphocyte- and natural killer cell-mediated cytotoxicity.

Cited by 31 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. A cell-based functional assay that accurately links genotype to phenotype in Familial HLH;Blood;2023-01-27

5. Neuroinflammation Associated With Inborn Errors of Immunity;Frontiers in Immunology;2022-01-19

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