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Persistent pulmonary arterial hypertension in the newborn (PPHN): a frequent manifestation of TMEM70 defective patients.
Catteruccia, Michela; Verrigni, Daniela; Martinelli, Diego; Torraco, Alessandra; Agovino, Teresa; Bonafé, Luisa; D'Amico, Adele; Donati, Maria Alice; Adorisio, Rachele; Santorelli, Filippo Maria; Carrozzo, Rosalba; Bertini, Enrico; Dionisi-Vici, Carlo.
Afiliação
  • Catteruccia M; Unit for Neuromuscular and Neurodegenerative Disorders, Laboratory of Molecular Medicine, Bambino Gesù Children's Hospital, Rome, Italy. Electronic address: michela.catteruccia@gmail.com.
  • Verrigni D; Unit for Neuromuscular and Neurodegenerative Disorders, Laboratory of Molecular Medicine, Bambino Gesù Children's Hospital, Rome, Italy.
  • Martinelli D; Unit of Metabolism, Bambino Gesù Children's Hospital, Rome, Italy.
  • Torraco A; Unit for Neuromuscular and Neurodegenerative Disorders, Laboratory of Molecular Medicine, Bambino Gesù Children's Hospital, Rome, Italy.
  • Agovino T; Metabolic and Muscular Unit, Neuroscience Department, Meyer Children's Hospital, Florence, Italy.
  • Bonafé L; Division of Molecular Pediatrics, Lausanne University Hospital, 1011 Lausanne, Switzerland.
  • D'Amico A; Unit for Neuromuscular and Neurodegenerative Disorders, Laboratory of Molecular Medicine, Bambino Gesù Children's Hospital, Rome, Italy.
  • Donati MA; Metabolic and Muscular Unit, Neuroscience Department, Meyer Children's Hospital, Florence, Italy.
  • Adorisio R; Heart Failure Unit, Department of Pediatric Cardiology and Cardiac Surgery, Bambino Gesù Children's Hospital, Rome Italy.
  • Santorelli FM; UOC Neurogenetica e Malattie Neuromuscolari, IRCCS Fondazione Stella Maris, Pisa, Italy.
  • Carrozzo R; Unit for Neuromuscular and Neurodegenerative Disorders, Laboratory of Molecular Medicine, Bambino Gesù Children's Hospital, Rome, Italy.
  • Bertini E; Unit for Neuromuscular and Neurodegenerative Disorders, Laboratory of Molecular Medicine, Bambino Gesù Children's Hospital, Rome, Italy.
  • Dionisi-Vici C; Unit of Metabolism, Bambino Gesù Children's Hospital, Rome, Italy.
Mol Genet Metab ; 111(3): 353-359, 2014 Mar.
Article em En | MEDLINE | ID: mdl-24485043
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cardiomiopatia Hipertrófica / Doenças Mitocondriais / Proteínas Mitocondriais / Hipertensão Pulmonar / Proteínas de Membrana Limite: Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2014 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cardiomiopatia Hipertrófica / Doenças Mitocondriais / Proteínas Mitocondriais / Hipertensão Pulmonar / Proteínas de Membrana Limite: Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2014 Tipo de documento: Article