Familial Behr syndrome-like phenotype with autosomal dominant inheritance-Reference-Cited by-同舟云学术

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Familial Behr syndrome-like phenotype with autosomal dominant inheritance

Published:2008-05 Issue:4 Volume:14 Page:370-372
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Felicio Andre C.,Godeiro-Junior Clecio,Alberto Lucianna G.,Pinto Aline P.M.,Sallum Juliana M.F.,Teive Helio G.,Barsottini Orlando G.P.

Publisher

Elsevier BV

Subject

Neurology (clinical),Geriatrics and Gerontology,Neurology

Reference11 articles.

1. Die komplizierte, hereditär-familiäre Optikusatrophie des Kindesalters: ein bisher nicht beschriebener Symptomkompleks;Behr;Klinische Monatsblätter für Augenheilkunde,1909

2. Behr's syndrome. A family exhibiting pseudodominant inheritance;Thomas;J Neurol Sci,1984

3. Behr syndrome variant with tremor treated by VIM stimulation;Schramm;Acta Neurochir,2005

4. Behr's syndrome and 3-methylglutaconic aciduria;Sheffer;Am J Ophthalmol,1992

5. 3-Methylglutaconic aciduria in optic atrophy;Costeff;Ann Neurol,1993

Cited by 8 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. Behr's syndrome mimicking a case of hereditary spastic paraparesis;eNeurologicalSci;2024-03

2. Concurrent OPA1 mutation and chromosome 3q deletion leading to Behr syndrome: a case report;BMC Pediatrics;2020-09-03

3. Optic Atrophy in Children;Pediatric Neuro-Ophthalmology;2016

4. Behr syndrome with homozygous C19ORF12 mutation;Journal of the Neurological Sciences;2015-10

5. Hereditary Optic Neuropathies;Optic Nerve Disorders;2014

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