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Congenital myopathy due to myosin heavy chain 2 mutation presenting as chronic aspiration pneumonia in infancy.
Tsabari, R; Daum, H; Kerem, E; Fellig, Y; Dor, T.
Affiliation
  • Tsabari R; Department of Pediatrics, Pediatric Pulmonology and Cystic Fibrosis Center, Hadassah-Hebrew University Medical Center Jerusalem, Israel.
  • Daum H; Department of Genetics and Metabolic Diseases, Hadassah-Hebrew University Medical Center Jerusalem, Israel.
  • Kerem E; Department of Pediatrics, Pediatric Pulmonology and Cystic Fibrosis Center, Hadassah-Hebrew University Medical Center Jerusalem, Israel.
  • Fellig Y; Department of Pathology, Hadassah-Hebrew-University-Medical-Center Jerusalem, Israel.
  • Dor T; Neuropediatric Unit, Hadassah-Hebrew University Medical Center Jerusalem, Israel. Electronic address: talyad@hadassah.org.il.
Neuromuscul Disord ; 27(10): 947-950, 2017 Oct.
Article in En | MEDLINE | ID: mdl-28729039
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pneumonia, Aspiration / Myosin Heavy Chains / Mutation / Myotonia Congenita Type of study: Diagnostic_studies Limits: Child / Humans / Infant / Male Language: En Journal: Neuromuscul Disord Journal subject: NEUROLOGIA Year: 2017 Document type: Article Affiliation country: Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pneumonia, Aspiration / Myosin Heavy Chains / Mutation / Myotonia Congenita Type of study: Diagnostic_studies Limits: Child / Humans / Infant / Male Language: En Journal: Neuromuscul Disord Journal subject: NEUROLOGIA Year: 2017 Document type: Article Affiliation country: Country of publication: