Neonatal vocal cord paralysis-an early presentation of hereditary neuralgic amyotrophy due to a mutation in the SEPT9 gene
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health
Reference9 articles.
1. The clinical spectrum of neuralgic amyotrophy in 246 cases;van Alfen;Brain,2006
2. Evidence for genetic heterogeneity in hereditary neuralgic amyotrophy;Watts;Neurology,2001
3. Phenotypic spectrum of hereditary neuralgic amyotrophy caused by the SEPT9 R88W mutation;Ueda;J Neurol Neurosurg Psychiatry,2001
4. Verpoorten N.Mutations in SEPT9 cause hereditary neuralgic amyotrophy;Kuhlenbäumer;Nat Genet,2005
5. SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy;Hannibal;Neurology,2009
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1. miR-124-3p regulates the proliferation and differentiation of retinal progenitor cells through SEPT10;Cell and Tissue Research;2023-02-21
2. Hereditary neuralgic amyotrophy in childhood caused by duplication within the SEPT9 gene: A family study;Cytoskeleton;2018-10-10
3. Infant brachial neuritis following a viral prodrome: a case in a 6-month old child and review of the literature;Child's Nervous System;2017-09-07
4. Pediatric Hereditary Neuralgic Amyotrophy;Child Neurology Open;2016-01-01
5. Familial congenital bilateral vocal fold paralysis: A novel gene translocation;International Journal of Pediatric Otorhinolaryngology;2015-03
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