Acute inflammatory demyelinating polyradiculoneuropathy associated with perforin-deficient familial haemophagocytic lymphohistiocytosis
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.2003.tb00566.x/fullpdf
Reference14 articles.
1. New concepts of Guillain-Barré syndrome;Asbury;J Child Neurol,2000
2. Infection- and malignancy-associated hemophagocytic syndromes. Secondary hemophagocytic lymphohistiocytosis;Janka;Hematol Oncol Clin North Am,1998
3. Perforin gene defects in familial hemopha-gocytic lymphohistiocytosis;Stepp;Science,1999
4. Further evidence for genetic heterogeneity in familial hemophagocytic lymphohistiocytosis;Graham;Pediatr Res,2000
5. Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis;Goransdotter Ericson;Am J Hum Genet,2001
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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. RF1 Gene Mutation in Familial Hemophagocytic Lymphohistiocytosis 2: A Family Report and Literature Review;Pharmacogenomics and Personalized Medicine;2021-12
3. CNS Involvement in HLH (CNS-HLH);Histiocytic Disorders;2017-11-19
4. Host genetics of Epstein–Barr virus infection, latency and disease;Reviews in Medical Virology;2014-11-27
5. Identification of Gene Networks and Pathways Associated with Guillain-Barré Syndrome;PLoS ONE;2012-01-10
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