Behr's Syndrome: Familial Optic Atrophy, Spastic Diplegia and Ataxia-Reference-Cited by-同舟云学术

Behr's Syndrome: Familial Optic Atrophy, Spastic Diplegia and Ataxia

Published:2008-11-12 Issue:1 Volume:15 Page:41-47
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:

Author:

Landrigan Philip J.,Berenberg William,Bresnan Michael

Publisher

Wiley

Subject

Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1973.tb04864.x/fullpdf

Reference34 articles.

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

2. Atrophie musculaire neurogène du type Charcot-Marie-Tooth-Hoffman, associée a une atrophie optique bilatérale;Brihaye;Acta Neurologica Psychiatrica Belgica,1956

3. Dominant juvenile optic atrophy. A study in two families and review of hereditary disease in childhood;Caldwell;Archives of Ophthalmology,1971

4. Optic atrophy in infancy, childhood and adolescence: a survey of 81 cases;Cordes;American Journal of Ophthalmology,1952

5. Muscle biopsies in neuromuscular diseases;Engel;Pediatric Clinics of North America,1967

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