Literature DB >> 5416261

Studies on a patient with hypokalemic familial periodic paralysis.

A M Gordon, J R Green, D Lagunoff.   

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Year:  1970        PMID： 5416261     DOI： 10.1016/0002-9343(70)90114-2

Source DB:  PubMed          Journal:  Am J Med        ISSN： 0002-9343            Impact factor:   4.965


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  4 in total

1.  Clinical and ultrastructural observations in a kindred with normo-hyperkalaemic periodic paralysis.

Authors:  T S Danowski; E R Fisher; C Vidalon; J W Vester; R Thompson; S Nolan; T Stephan; J H Sunder
Journal:  J Med Genet       Date:  1975-03       Impact factor: 6.318

2.  Familial thyrotoxic periodic paralysis.

Authors:  W M Kufs; M McBiles; T Jurney
Journal:  West J Med       Date:  1989-04

3.  Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis.

Authors:  R H Boerman; R A Ophoff; T P Links; R van Eijk; L A Sandkuijl; A Elbaz; J E Vale-Santos; A R Wintzen; J C van Deutekom; D E Isles
Journal:  J Med Genet       Date:  1995-01       Impact factor: 6.318

4.  Effects of potassium depletion and insulin on resting and stimulated skeletal rat muscle.

Authors:  R Dengler; W W Hofmann; R Rüdel
Journal:  J Neurol Neurosurg Psychiatry       Date:  1979-09       Impact factor: 10.154
  4 in total

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