Literature DB >> 13823698

Unusual familial occurrence of myasthenia gravis.

F F FOLDES, P G McNALL.   

Abstract

Entities:  

Keywords:  MYASTHENIA GRAVIS/genetics

Mesh：

Year:  1960        PMID： 13823698     DOI： 10.1001/jama.1960.63030040024021c

Source DB:  PubMed          Journal:  JAMA        ISSN： 0098-7484            Impact factor:   56.272


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  6 in total

1.  The clinical study and HLA genotyping of 112 familial myasthenia gravis patients.

Authors:  B Bu; M Yang; J Xu; F Gong; X Jiang; X Nie
Journal:  J Tongji Med Univ       Date:  1999

2.  Genetic study of sample of 70 patients with myasthenia gravis.

Authors:  A Jacob; E R Clack; A E Emery
Journal:  J Med Genet       Date:  1968-12       Impact factor: 6.318

3.  Whole-exome sequencing reveals a rare interferon gamma receptor 1 mutation associated with myasthenia gravis.

Authors:  Guoyan Qi; Peng Liu; Shanshan Gu; Hongxia Yang; Huimin Dong; Yinping Xue
Journal:  Neurol Sci       Date:  2018-02-13       Impact factor: 3.307

4.  Immune disease and HLA associations with myasthenia gravis.

Authors:  P O Behan
Journal:  J Neurol Neurosurg Psychiatry       Date:  1980-07       Impact factor: 10.154

5.  Familial myasthenia gravis.

Authors:  C B Warrier; T D Pillai
Journal:  Br Med J       Date:  1967-09-30

6.  A genetic study of infantile and juvenile myasthenia gravis.

Authors:  S Bundey
Journal:  J Neurol Neurosurg Psychiatry       Date:  1972-02       Impact factor: 10.154
  6 in total

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