(Q73299439)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

title

Genotype-phenotype correlations of DHP receptor alpha 1-subunit gene mutations causing hypokalemic periodic paralysis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

hypokalemic periodic paralysis

2 November 2019

main subject

1 reference

1 reference

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

author name string

G Fouad

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

M Dalakas

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

S Servidei

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

J R Mendell

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

P Van den Bergh

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

K Alderson

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

R C Griggs

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

R Tawil

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

R Gregg

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

K Hogan

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

P A Powers

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

N Weinberg

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

W Malonee

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

L J Ptácek

15

1 reference

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2 November 2019

publication date

1 January 1997

1 reference

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2 November 2019

published in

Neuromuscular Disorders

1 reference

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2 November 2019

volume

7

1 reference

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2 November 2019

issue

1

1 reference

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2 November 2019

page(s)

33-38

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

2 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900401-4

7 January 2021

The periodic paralyses

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900401-4

7 January 2021

Permanent muscle weakness in familial hypokalaemic periodic paralysis. Clinical, radiological and pathological aspects

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900401-4

7 January 2021

Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900401-4

7 January 2021

Assignment of the human gene for the alpha 1 subunit of the skeletal muscle DHP-sensitive Ca2+ channel (CACNL1A3) to chromosome 1q31-q32

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900401-4

7 January 2021

A calcium channel mutation causing hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900401-4

7 January 2021

Intermittent muscular weakness, extrasystoles, and multiple developmental anomalies. A new syndrome?

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900401-4

7 January 2021

Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900401-4

7 January 2021

Potentially fatal cardiac dysrhythmia and hyperkalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900401-4

7 January 2021

Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900401-4

7 January 2021

Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900401-4

7 January 2021

The structure of the gene encoding the human skeletal muscle alpha 1 subunit of the dihydropyridine-sensitive L-type calcium channel (CACNL1A3)

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900401-4

7 January 2021

Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900401-4

7 January 2021

Calcium and ischemic injury

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900401-4

7 January 2021

The sarcoplasmic reticulum in thyrotoxic hypoxalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900401-4

7 January 2021

Mitochondrial calcium overload: A general mechanism for cell-necrosis in muscle diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900401-4

7 January 2021

10.1016/S0960-8966(96)00401-4

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9132138%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference