(Q31036270)

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Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17.

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scholarly article

1 reference

Europe PubMed Central

28 June 2017

Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17. (English)

1 reference

Europe PubMed Central

28 June 2017

periodic paralysis

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based on heuristic

inferred from title

hyperkalemic periodic paralysis

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based on heuristic

inferred from title

paramyotonia congenita

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author name string

Koch MC

1

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Europe PubMed Central

28 June 2017

Ricker K

2

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Europe PubMed Central

28 June 2017

Otto M

3

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Europe PubMed Central

28 June 2017

Grimm T

4

1 reference

Europe PubMed Central

28 June 2017

Bender K

5

1 reference

Europe PubMed Central

28 June 2017

Zoll B

6

1 reference

Europe PubMed Central

28 June 2017

Harper PS

7

1 reference

Europe PubMed Central

28 June 2017

Lehmann-Horn F

8

1 reference

Europe PubMed Central

28 June 2017

Rüdel R

9

1 reference

Europe PubMed Central

28 June 2017

Hoffman EP

10

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Europe PubMed Central

28 June 2017

publication date

1 November 1991

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Europe PubMed Central

28 June 2017

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Europe PubMed Central

28 June 2017

88

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28 June 2017

71-74

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1

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28 June 2017

Strategies for multilocus linkage analysis in humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patterns of polymorphism and linkage disequilibrium suggest independent origins of the human growth hormone gene cluster

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https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

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A simple salting out procedure for extracting DNA from human nucleated cells

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https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paramyotonia congenita: a clinical, histochemical and pathological study

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Membrane defects in paramyotonia congenita (Eulenburg)

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two cases of adynamia episodica hereditaria: In vitro investigation of muscle cell membrane and contraction parameters

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered gating and conductance of Na+ channels in hyperkalemic periodic paralysis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Membrane defects in paramyotonia congenita with and without myotonia in a warm environment.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adynamia episodica hereditaria with myotonia: a non-inactivating sodium current and the effect of extracellular pH

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Membrane changes in cells from myotonia patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital paramyotonia, adynamia episodica hereditaria, or familial periodic paralysis with paramyotonia and hyperkalemia (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adynamia episodica hereditaria: what causes the weakness?

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paramyotonia congenita or hyperkalemic periodic paralysis? Clinical and electrophysiological features of each entity in one family

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myotonia fluctuans

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of a human skeletal muscle sodium channel α-subunit gene (SCN4A) to 17q23.1–25.3

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Potassium uptake in muscle during paramyotonic weakness.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adynamia episodica and paralysis periodica paramyotonica

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adynamia episodica hereditaria and myotonia

1 reference

https://pubmed.ncbi.nlm.nih.gov/1660029

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00204932

1 reference

Europe PubMed Central

28 June 2017

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

28 June 2017

Springer Nature article ID

10.1007/bf00204932

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