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Spinocerebellar Degeneration
Known as:
Spinocerebellar Diseases
, Spino-Cerebellar Degenerations
, Degenerations, Spinocerebellar
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A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic…
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National Institutes of Health
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Related topics
Related topics
42 relations
Broader (5)
Ataxia
Ataxias, Hereditary
Degenerative Diseases, Central Nervous System
Neurodegenerative Disorders
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Narrower (29)
Ataxia Telangiectasia
Cerebellar Ataxia
Cerebellar Ataxia, Early Onset
Cerebellar Ataxia, Late Onset
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Ataxia, Spinocerebellar
Degeneration of cerebellum
In Blood
Microbiological
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
On the real locus in the Kato-Nakayama space of logarithmic spaces with a view toward toric degenerations
Hülya Argüz
,
Bernd S Siebert
2016
Corpus ID: 119578571
We study the real loci of toric degenerations of complex varieties with reducible central fibre, as introduced in the joint work…
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2004
2004
Zur Histopathologie und Klinik der Spätform von amaurotischer Idiotie
F. Seitelberger
,
K. Nagy
Deutsche Zeitschrift für Nervenheilkunde
2004
Corpus ID: 39250161
Die Spi~tfalle von amaurotischer Idiotie (a. I.), die seit KIIFS (1925) als eigene Form zusammengefai3t werden, verdienen trotz…
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1997
1997
Frontotemporal degeneration, Pick disease, and corticobasal degeneration. Three entities or 1?
V. Hachinski
Archives of Neurology
1997
Corpus ID: 27591922
The brainfunctions with bewildering complexity, but fails in only a few ways. This makes prognosis easier but classification…
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1989
1989
Normal cerebellar glutamate dehydrogenase protein in spinocerebellar degeneration.
R. Rosenberg
,
Carl BANNERt
Journal of Neurology Neurosurgery & Psychiatry
1989
Corpus ID: 1110170
Immunochemical analyses (Western blots) of cerebellar homogenates for glutamate dehydrogenase (GDH) from patients with…
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1988
1988
Hexosaminidase A deficiency presenting as juvenile progressive dystonia.
R. Hardie
,
E. Young
,
J. Morgan-Hughes
Journal of Neurology Neurosurgery & Psychiatry
1988
Corpus ID: 26725466
Sir: Hexosaminidase A deficiency is an inherited disorder characterised by the accumulation of GM2-ganglioside in cerebral and…
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1985
1985
Familial spinocerebellar degeneration with corneal dystrophy.
V. D. Der Kaloustian
,
N. Jarudi
,
+5 authors
M. Mikati
American journal of medical genetics
1985
Corpus ID: 33944590
We report on two sisters born to normal but consanguineous parents, with the unusual combination of spinocerebellar degeneration…
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1967
1967
Neural mechanisms of the chloralose jerk with special reference to its relationship with the spino-bulbo-spinal reflex.
M. Shimamura
,
T. Yamauchi
The Japanese Journal of Physiology
1967
Corpus ID: 12499275
1. Experiments were performed on 26 adult cats under chloralose anesthesia, in order to investigate whether a relationship exists…
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Review
1964
Review
1964
Les heredo-degenerescences chorio-retiniennes.
Francis A. L'Esperance
1964
Corpus ID: 73263229
The Hereditary Chorioretinal Degenerations (Tapetoretinal Degenerations) is a communication sponsored by the Societe Francaise d…
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1958
1958
The differential diagnosis of tapetoretinal degenerations.
J. François
A M A Archives of Ophthalmology
1958
Corpus ID: 20464357
1. Definition of Tapetoretinal Degenerations Tapetoretinal degenerations are due to partial or complete destruction of a normally…
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1939
1939
Die Atrophie des Systems des Brückenfußes und der unteren Oliven
E. Welte
European Archives of Psychiatry and Neurological…
1939
Corpus ID: 44340503
ZusammenfassungI.Die Atrophie des Systems des Brückenfußes und der unteren Oliven (3 eigene Fälle) ist eine „eigentliche…
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