(Q41834424)

English

CEREBELLO-THALAMO-SPINAL DEGENERATION IN INFANCY: AN UNUSUAL VARIANT OF WERDNIG-HOFFMANN DISEASE.

scientific article published on June 1965

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Europe PubMed Central

12 October 2017

CEREBELLO-THALAMO-SPINAL DEGENERATION IN INFANCY: AN UNUSUAL VARIANT OF WERDNIG-HOFFMANN DISEASE. (English)

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Europe PubMed Central

12 October 2017

NORMAN RM

1

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Europe PubMed Central

PMC publication ID

2019395

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12 October 2017

KAY JM

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2

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Europe PubMed Central

PMC publication ID

2019395

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12 October 2017

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English

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1 June 1965

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Europe PubMed Central

12 October 2017

Archives of Disease in Childhood

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Europe PubMed Central

12 October 2017

40

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Europe PubMed Central

12 October 2017

302-308

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Europe PubMed Central

12 October 2017

Cerebellar hypoplasia in Werdnig-Hoffmann disease

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019395

retrieved

6 June 2018

[Spinal amyotrophia in children (Werdnig-Hoffmann paralysis) as hereditary degeneration.]

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/14294750

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12 December 2020

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inferred from PubMed ID database lookup

[Forty cases of Werdnig-Hoffmann disease with eleven anatomical examinations]

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14294750

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12 December 2020

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Identifiers

DOI

10.1136/ADC.40.211.302

1 reference

stated in

Europe PubMed Central

12 October 2017

1 reference

Europe PubMed Central

PMC publication ID

2019395

retrieved

12 October 2017

PubMed publication ID

14294750

1 reference

stated in

Europe PubMed Central

PMC publication ID

2019395

retrieved

12 October 2017

ResearchGate publication ID

9288983

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(Q41834424)

CEREBELLO-THALAMO-SPINAL DEGENERATION IN INFANCY: AN UNUSUAL VARIANT OF WERDNIG-HOFFMANN DISEASE.

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