Literature DB >> 5345117

Neurogenic muscular atrophy simulating facioscapulohumeral muscular dystrophy with particular reference to the heterogeneity of Kugelberg-Welander disease.

T Furukawa, H Tsukagoshi, H Sugita, Y Toyokura.   

Abstract

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Year:  1969        PMID： 5345117     DOI： 10.1016/0022-510x(69)90082-3

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN： 0022-510X            Impact factor:   3.181


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  4 in total

Review 1.  The nosology of the spinal muscular atrophies.

Authors:  A E Emery
Journal:  J Med Genet       Date:  1971-12       Impact factor: 6.318

2.  Chronic spinal muscular atrophy of facioscapulohumeral type.

Authors:  T Furukawa; Y Toyokura
Journal:  J Med Genet       Date:  1976-08       Impact factor: 6.318

3.  Morpholino treatment improves muscle function and pathology of Pitx1 transgenic mice.

Authors:  Sachchida Nand Pandey; Yi-Chien Lee; Toshifumi Yokota; Yi-Wen Chen
Journal:  Mol Ther       Date:  2013-11-14       Impact factor: 11.454

4.  Conditional over-expression of PITX1 causes skeletal muscle dystrophy in mice.

Authors:  Sachchida N Pandey; Jennifer Cabotage; Rongye Shi; Manjusha Dixit; Margret Sutherland; Jian Liu; Stephanie Muger; Scott Q Harper; Kanneboyina Nagaraju; Yi-Wen Chen
Journal:  Biol Open       Date:  2012-05-25       Impact factor: 2.422
  4 in total

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