Progressive Encephalopathy with Edema, Hypsarrhythmia, and Optic Atrophy (PEHO Syndrome) in Two Japanese Siblings
Author:
Publisher
Georg Thieme Verlag KG
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2007-979771.pdf
Cited by 21 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. Refining the phenotypic spectrum of CCDC88A‐related PEHO‐like syndrome;American Journal of Medical Genetics Part A;2023-10-05
2. Clinical and genetic features of PEHO and PEHO-Like syndromes: A scoping review;Biomedicine & Pharmacotherapy;2020-11
3. A novel homozygous nonsense mutation in CCDC88A gene cause PEHO-like syndrome in consanguineous Saudi family;Neurological Sciences;2018-11-03
4. PEHO syndrome: the endpoint of different genetic epilepsies;Journal of Medical Genetics;2018-10-04
5. The phenotypic and molecular spectrum of PEHO syndrome and PEHO-like disorders;Brain;2017-07-12
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