(Q39511490)

English

Transient muscular weakness in severe recessive myotonia congenita. Improvement of isometric muscle force by drugs relieving myotomic stiffness

scientific article published on August 1978

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

Transient muscular weakness in severe recessive myotonia congenita. Improvement of isometric muscle force by drugs relieving myotomic stiffness (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

author name string

K Ricker

1

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

A Haass

2

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

G Hertel

3

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

H G Mertens

4

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

publication date

1 August 1978

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Europe PubMed Central

PubMed publication ID

12 September 2017

Journal of Neurology

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Europe PubMed Central

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12 September 2017

218

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Europe PubMed Central

PubMed publication ID

12 September 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

253-262

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

Electromyographic studies in myotonia congenita

1 reference

https://pubmed.ncbi.nlm.nih.gov/81274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and electrophysiological observations in patients with myotonic muscle disease and the therapeutic effect of N-propyl-ajmalin

1 reference

https://pubmed.ncbi.nlm.nih.gov/81274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Neurophysiological studies on the temporary paresis in myotonia congenita and dystrophia myotonica]

1 reference

https://pubmed.ncbi.nlm.nih.gov/81274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscular weakness corrected by exercise accompanying a muscular hypertrophy with myotonia

1 reference

https://pubmed.ncbi.nlm.nih.gov/81274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscular paralysis in myotonia congenita

1 reference

https://pubmed.ncbi.nlm.nih.gov/81274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The declining electrical response of muscle to repetitive nerve stimulation in myotonia

1 reference

https://pubmed.ncbi.nlm.nih.gov/81274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial case of myotonia with muscular hypertrophy, weakness corrected by effort and atrophy of type II fibers

1 reference

https://pubmed.ncbi.nlm.nih.gov/81274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Weakness in myotonic syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/81274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Congenital myotonia, muscular weakness treated by exertion and muscular hypertrophy]

1 reference

https://pubmed.ncbi.nlm.nih.gov/81274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On the repetitive discharge in myotonic muscle fibres

1 reference

https://pubmed.ncbi.nlm.nih.gov/81274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscle weakness after rest in myotonic disorders; an electrophysiological study

1 reference

https://pubmed.ncbi.nlm.nih.gov/81274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recessively inherited myotonia congenita

1 reference

https://pubmed.ncbi.nlm.nih.gov/81274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuromuscular Failure in Myotonic Rats

1 reference

https://pubmed.ncbi.nlm.nih.gov/81274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00312881

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

release_zx3ylmlvyjbgdae2g2w3t3fbsi

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 September 2017

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