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Primary Carnitine Deficiency - A Rare Treatable Cause of Cardiomyopathy and Massive Hepatomegaly.
Deswal, Shivani; Bijarnia-Mahay, Sunita; Manocha, Vinamr; Hara, Keiichi; Shigematsu, Yosuke; Saxena, Renu; Verma, Ishwar C.
Afiliación
  • Deswal S; Department of Pediatrics, PGIMER and Dr. RML Hospital, New Delhi, India. shivanipaeds@gmail.com.
  • Bijarnia-Mahay S; Institute of Medical Genetics & Genomics, Sir Ganga Ram Hospital, New Delhi, India.
  • Manocha V; Department of Pediatrics, PGIMER and Dr. RML Hospital, New Delhi, India.
  • Hara K; Department of Pediatrics, The National Hospital Organization Kure Medical Center, Aoyama-Cho, Kure City, Hiroshima, Japan.
  • Shigematsu Y; Department of Pediatrics, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.
  • Saxena R; Institute of Medical Genetics & Genomics, Sir Ganga Ram Hospital, New Delhi, India.
  • Verma IC; Institute of Medical Genetics & Genomics, Sir Ganga Ram Hospital, New Delhi, India.
Indian J Pediatr ; 84(1): 83-85, 2017 Jan.
Article en En | MEDLINE | ID: mdl-27581592
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Carnitina / Hiperamonemia / Hepatomegalia / Enfermedades Musculares / Cardiomiopatías Idioma: En Revista: Indian J Pediatr Año: 2017 Tipo del documento: Article País de afiliación: India
Texto completo
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Carnitina / Hiperamonemia / Hepatomegalia / Enfermedades Musculares / Cardiomiopatías Idioma: En Revista: Indian J Pediatr Año: 2017 Tipo del documento: Article País de afiliación: India