Literature DB >> 5820859

Pathology of muscular hypotonia in the Prader-Willi syndrome. Light and electron microscopic study.

A K Afifi, H Zellweger.   

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Year:  1969        PMID： 5820859     DOI： 10.1016/0022-510x(69)90058-6

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


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  4 in total

1.  The Prader-Willi syndrome with a 15/15 translocation. Case report and review of the literature.

Authors:  C J Hawkey; A Smithies
Journal:  J Med Genet       Date:  1976-04       Impact factor: 6.318

2.  A possible role for electron microscopy in detection of carriers of Duchenne type muscular dystrophy.

Authors:  A K Afifi; R A Bergman; H Zellweger
Journal:  J Neurol Neurosurg Psychiatry       Date:  1973-08       Impact factor: 10.154

3.  Prader-Willi syndrome: current understanding of cause and diagnosis.

Authors:  M G Butler
Journal:  Am J Med Genet       Date:  1990-03

4.  One Year of Recombinant Human Growth Hormone Treatment in Adults with Prader-Willi Syndrome Improves Body Composition, Motor Skills and Brain Functional Activity in the Cerebellum.

Authors:  Laia Casamitjana; Laura Blanco-Hinojo; Olga Giménez-Palop; Jesús Pujol; Gerard Martínez-Vilavella; Susanna Esteba-Castillo; Rocío Pareja; Valentín Freijo; Laura Vigil; Joan Deus; Assumpta Caixàs
Journal:  J Clin Med       Date:  2022-03-25       Impact factor: 4.241
  4 in total

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