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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
1999-2-25
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pubmed:abstractText |
X-linked myotubular myopathy (MTM1) is a rare developmental disorder of skeletal muscle characterized by the presence of central nuclei in biopsy specimens from affected male subjects. Until recently, the disorder was usually fatal within the first year of life. This study was undertaken to determine the outcome in long-term survivors (>1 year of age) with MTM1.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0022-3476
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
134
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
206-14
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:9931531-Adolescent,
pubmed-meshheading:9931531-Adult,
pubmed-meshheading:9931531-Child,
pubmed-meshheading:9931531-Child, Preschool,
pubmed-meshheading:9931531-Cognition,
pubmed-meshheading:9931531-Gastrointestinal Diseases,
pubmed-meshheading:9931531-Genetic Linkage,
pubmed-meshheading:9931531-Growth,
pubmed-meshheading:9931531-Hematologic Diseases,
pubmed-meshheading:9931531-Humans,
pubmed-meshheading:9931531-Infant,
pubmed-meshheading:9931531-Male,
pubmed-meshheading:9931531-Muscle, Skeletal,
pubmed-meshheading:9931531-Muscular Diseases,
pubmed-meshheading:9931531-Mutation,
pubmed-meshheading:9931531-Prognosis,
pubmed-meshheading:9931531-Protein Tyrosine Phosphatases,
pubmed-meshheading:9931531-Protein Tyrosine Phosphatases, Non-Receptor,
pubmed-meshheading:9931531-Psychomotor Performance,
pubmed-meshheading:9931531-Respiratory Tract Diseases,
pubmed-meshheading:9931531-Survivors,
pubmed-meshheading:9931531-X Chromosome
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pubmed:year |
1999
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pubmed:articleTitle |
Medical complications in long-term survivors with X-linked myotubular myopathy.
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pubmed:affiliation |
Children's Hospital Research Foundation, Columbus, OH 43206, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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