Classification of the hereditary ataxias and paraplegias (Q34247421)

31 July 2017

title

Classification of the hereditary ataxias and paraplegias (English)

1 reference

31 July 2017

A. E. Harding

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6133167

11 August 2023

language of work or name

English

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publication date

1 May 1983

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31 July 2017

21 May 1983

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National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=6133167

full work available at URL

11 August 2023

https://api.elsevier.com/content/article/PII:S0140673683928799?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(83)92879-9

https://api.elsevier.com/content/article/PII:S0140673683928799?httpAccept=text/plain

11 August 2023

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(83)92879-9

11 August 2023

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31 July 2017

volume

1

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31 July 2017

issue

8334

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31 July 2017

page(s)

1151-1155

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AN ATTEMPT TO CLASSIFY CEREBELLAR DISEASE, WITH A NOTE ON MARIE'S HEREDITARY CEREBELLAR ATAXIA

31 July 2017

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Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families

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Glutamate dehydrogenase deficiency in three patients with spinocerebellar syndrome

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Clinical Studies of a Patient With Pyruvate Decarboxylase Deficiency

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Early onset cerebellar ataxia with retained tendon reflexes: a clinical and genetic study of a disorder distinct from Friedreich's ataxia

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A new familial syndrome with ataxia, hearing loss, and mental retardation. Report of three brothers

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HEREDITARY CEREBELLAR ATAXIA, MENTAL DEFICIENCY, PYRAMIDAL INVOLVEMENT AND MACULAR PIGMENTATION. A BRIEF REVIEW WITH REPORT OF TWO CASES.

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Familial spastic ataxia: Occurrence in childhood

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Marinesco-Sjögren syndrome. Report of an autopsy

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DYSSYNERGIA CEREBELLARIS MYOCLONICA—PRIMARY ATROPHY OF THE DENTATE SYSTEM: A CONTRIBUTION TO THE PATHOLOGY AND SYMPTOMATOLOGY OF THE CEREBELLUM

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Progressive myoclonus and epilepsy with dentatorubral degeneration: a clinicopathological study of the Ramsay Hunt syndrome

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A spinocerebellar degeneration with X-linked inheritance

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Autosomal dominant system degeneration in Portuguese families of the Azores Islands. A new genetic disorder involving cerebellar, pyramidal, extrapyramidal and spinal cord motor functions

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Strumpell's pure familial spastic paraplegia: case study and review of the literature

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7 January 2021

Familial spastic paraplegia with amyotrophy of the hands

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Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations

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The Troyer syndrome. A recessive form of spastic paraplegia with distal muscle wasting

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11 August 2023

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A sex-linked recessive form of spastic paraplegia

11 August 2023

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OBSERVATIONS ON ESSENTIAL (HEREDOFAMILIAL) TREMOR

11 August 2023

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Two kindreds with a sex-linked recessive form of spastic paraplegia

11 August 2023

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Juvenile amyotrophic lateral sclerosis in two brothers from an inbred community

11 August 2023

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11 August 2023

Identifiers

1 reference

31 July 2017

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