Progressive myoclonus epilepsy. A variant with probable X-linked inheritance (Q39677198)

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scientific article published on May 1979

Language	Label	Description	Also known as
English	Progressive myoclonus epilepsy. A variant with probable X-linked inheritance	scientific article published on May 1979

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Progressive myoclonus epilepsy. A variant with probable X-linked inheritance (English)

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

author name string

T F Wienker

1

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

G M von Reutern

2

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

H H Ropers

3

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

publication date

1 May 1979

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

49

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

83-89

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

ON GENETICS OF ESSENTIAL MYOCLONUS

1 reference

https://pubmed.ncbi.nlm.nih.gov/112032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On genetics of progressive myoclonic epilepsies (Unverricht-Lundborg)

1 reference

https://pubmed.ncbi.nlm.nih.gov/112032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cherry red spot-myoclonus syndrome: a newly recognized inherited lysosomal storage disease due to acid neuraminidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/112032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for preferential X-chromosome inactivation in a family with Fabry disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/112032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The manifesting carrier in Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/112032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Christmas disease in one of a pair of monozygotic twin girls, possibly the effect of lyonization

1 reference

https://pubmed.ncbi.nlm.nih.gov/112032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mucolipidosis I: increased sialic acid content and deficiency of an alpha-N-acetylneuraminidase in cultured fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/112032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The basic hereditary myoclonus-epilepsy-dementia syndromes. Progressive myoclonus epilepsies--myoclonic cerebellar dyssynergia--myoclonic variants of the 3 postinfantile types of amaurotic idiocy

1 reference

https://pubmed.ncbi.nlm.nih.gov/112032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myoclonus epilepsy (Univerricht-Lundborg) in Finland

1 reference

https://pubmed.ncbi.nlm.nih.gov/112032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

LAFORA'S DISEASE. DISTINCT CLINICO-PATHOLOGIC FORM OF UNVERRICHT'S SYNDROME.

1 reference

https://pubmed.ncbi.nlm.nih.gov/112032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

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