Diagnosis of Congenital Muscular Dystrophy

Open Access

|Apr 1996

Connolly AM Pestronk A Planer GJ Yue J Mehta S Choksi R Congenital muscular dystrophy syndromes distinguished by alkaline and acid phosphatase, merosin, and dystrophin staining Neurology 1996 Mar 46 3 810 14 10.1212/WNL.46.3.810 8618688
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Kobayashi O Hayashi Y Arahata K Ozawa E Nonaka I Congenital muscular dystrophy: Clinical and pathologic study of 50 patients with the classical (Occidental) merosin-positive form Neurology 1996 Mar 46 3 815 8 10.1212/WNL.46.3.815 8618689
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North KN Miller G Iannaccone ST Clemens PR Chad DA Bella I Cognitive dysfunction as the major presenting feature of Becker’s muscular dystrophy Neurology 1996 Feb 46 2 461 5 10.1212/WNL.46.2.461 8614513
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Language: English

Page range: 31 - 32

Published on: Apr 1, 1996

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

© 1996 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.