(Q34247421)

31 July 2017

Classification of the hereditary ataxias and paraplegias (English)

1 reference

31 July 2017

A. E. Harding

1

1 reference

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

0 references

publication date

1 May 1983

1 reference

31 July 2017

21 May 1983

1 reference

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

1 reference

31 July 2017

1

1 reference

31 July 2017

8334

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31 July 2017

1151-1155

1 reference

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

31 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

"Idiopathic" late onset cerebellar ataxia. A clinical and genetic study of 36 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Chronic GM2 gangliosidosis masquerading as atypical Friedreich ataxia: clinical, morphologic, and biochemical studies of nine cases

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Glutamate dehydrogenase deficiency in three patients with spinocerebellar syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Familial cerebrotendinous xanthomatosis. Report of a new family and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Clinical Studies of a Patient With Pyruvate Decarboxylase Deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal amino-aciduria, and other bizarre biochemical features

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Intermittent branched-chain ketonuria. Variant of maple-syrup-urine disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Xeroderma pigmentosum. An inherited diseases with sun sensitivity, multiple cutaneous neoplasms, and abnormal DNA repair

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Cockayne syndrome: Unusual neuropathological findings and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Ueber degenerative Atrophie der spinalen Hinterstränge

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Ueber degenerative Atrophie der spinalen Hinterstränge

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Quebec Cooperative Study of Friedreich's Ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Familial ataxia, deaf-mutism, and muscular wasting

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Familial spastic ataxia: Occurrence in childhood

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Behr syndrome: A clinicopathologic report

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Marinesco-Sjögren syndrome. Report of an autopsy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

A spinocerebellar degeneration with X-linked inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Observations on essential (heredofamial) tremor.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Hereditary olivopontocerebellar atrophy with retinal degeneration. Report of a family through six generations.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Familial myoclonus, cerebellar ataxia, and deafness. Specific genetically-determined disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Familial spastic paraplegia with amyotrophy of the hands

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Familial Spastic Paraplegia with Amyotrophy, Oligophrenia, and Central Retinal Degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

FAMILIAL AMYOTROPHIC DYSTONIC PARAPLEGIA

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Hereditary spastic paraparesis with sensory neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Hereditary sensory neuropathy with spastic paraplegia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

The mast syndrome. A recessively inherited form of presenile dementia with motor disturbances

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Hereditary spastic paraplegia in Western Norway.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Disordered pigmentation, spastic paraparesis and peripheral neuropathy in three siblings: a new neurocutaneous syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

Familial spastic paraplegia, peroneal neuropathy, and crural hypopigmentation: a new neurocutaneous syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

A family with hereditary ataxia: HLA typing

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2883%2992879-9

7 January 2021

The olivopontocerebellar atrophies: a review

4

1 reference

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

Quebec Cooperative Study on Friedreich's Ataxia

11 August 2023

32

1 reference

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

A sex-linked recessive form of spastic paraplegia

11 August 2023

45

1 reference

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

OBSERVATIONS ON ESSENTIAL (HEREDOFAMILIAL) TREMOR

11 August 2023

46

1 reference

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

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

11 August 2023

52

1 reference

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

Juvenile amyotrophic lateral sclerosis in two brothers from an inbred community

11 August 2023

57

1 reference

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

11 August 2023

Identifiers

1 reference

31 July 2017

1 reference