Kjellin Syndrome: Long-term Neuro-ophthalmologic Follow-up and Novel Mutations in the SPG11 Gene-Reference-Cited by-同舟云学术

Kjellin Syndrome: Long-term Neuro-ophthalmologic Follow-up and Novel Mutations in the SPG11 Gene

Published:2011-03 Issue:3 Volume:118 Page:564-573
ISSN:0161-6420
Container-title:Ophthalmology
language:en
Short-container-title:Ophthalmology

Author:

Puech Bernard,Lacour Arnaud,Stevanin Giovanni,Sautiere Bruno G.,Devos David,Depienne Christel,Denis Elodie,Mundwiller Emeline,Ferriby Didier,Vermersch Patrick,Defoort-Dhellemmes Sabine

Publisher

Elsevier BV

Subject

Ophthalmology

Reference19 articles.

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2. Sur une paraplegic spasmodique avec dégénérescence maculaire chez deux frères;Louis-Bar;Ophthalmologica,1945

3. Familial spastic paraplegia with amyotrophy, oligophrenia, and central retinal degeneration;Kjellin;Arch Neurol,1959

4. Fleck retina in Kjellin's syndrome;Farmer;Am J Ophthalmol,1985

5. Kjellin's syndrome: fundus autofluorescence, angiographic, and electrophysiologic findings;Frisch;Ophthalmology,2002

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5. SPG11: clinical and genetic features of seven Czech patients and literature review;Neurological Research;2022-03-07