Literature DB >> 10227611

Mutations of sodium channels in periodic paralysis: can they explain the disease and predict treatment?

R C Griggs, L J Ptácek.   

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Year:  1999        PMID： 10227611     DOI： 10.1212/wnl.52.7.1309

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  3 in total

1.  Phenotypic variation of a Thr704Met mutation in skeletal sodium channel gene in a family with paralysis periodica paramyotonica.

Authors:  J Kim; Y Hahn; E H Sohn; Y J Lee; J H Yun; J M Kim; J H Chung
Journal:  J Neurol Neurosurg Psychiatry       Date:  2001-05       Impact factor: 10.154

2.  Different flecainide sensitivity of hNav1.4 channels and myotonic mutants explained by state-dependent block.

Authors:  Jean-François Desaphy; Annamaria De Luca; Maria Paola Didonna; Alfred L George; Diana Camerino Conte; Annamaria D E Luca
Journal:  J Physiol       Date:  2003-11-07       Impact factor: 5.182

3.  Differential diagnosis of hyperkalemia: an update to a complex problem.

Authors:  T Eleftheriadis; K Leivaditis; G Antoniadi; V Liakopoulos
Journal:  Hippokratia       Date:  2012-10       Impact factor: 0.471
  3 in total

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