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One Year of Newborn Screening for SMA - Results of a German Pilot Project.
Vill, Katharina; Kölbel, Heike; Schwartz, Oliver; Blaschek, Astrid; Olgemöller, Bernhard; Harms, Erik; Burggraf, Siegfried; Röschinger, Wulf; Durner, Jürgen; Gläser, Dieter; Nennstiel, Uta; Wirth, Brunhilde; Schara, Ulrike; Jensen, Beate; Becker, Marc; Hohenfellner, Katharina; Müller-Felber, Wolfgang.
Afiliação
  • Vill K; Department of Pediatric Neurology and Developmental Medicine, Dr. v. Hauner Children's Hospital, LMU - University of Munich, Munich, Germany.
  • Kölbel H; Department of Pediatric Neurology, Developmental Neurology and Social Pediatrics, University of Essen, Germany.
  • Schwartz O; Department of Pediatric Neurology, Muenster University Hospital, Münster, Germany.
  • Blaschek A; Department of Pediatric Neurology and Developmental Medicine, Dr. v. Hauner Children's Hospital, LMU - University of Munich, Munich, Germany.
  • Olgemöller B; Previously Labor Becker, Olgemöller & Kollegen, Munich, Germany.
  • Harms E; Department of Pediatric Medicine, Previously Muenster University Hospital, Münster, Germany.
  • Burggraf S; Labor Becker & Kollegen, Munich, Germany.
  • Röschinger W; Labor Becker & Kollegen, Munich, Germany.
  • Durner J; Labor Becker & Kollegen, Munich, Germany.
  • Gläser D; Genetikum®, Center for Human Genetics, Neu-Ulm, Germany.
  • Nennstiel U; Screening Center of the Bavarian Health and Food Safety Authority, Oberschleissheim, Germany.
  • Wirth B; Institute of Human Genetics, University of Cologne, Cologne, Germany.
  • Schara U; Department of Pediatric Neurology, Developmental Neurology and Social Pediatrics, University of Essen, Germany.
  • Jensen B; Department of Pediatric Neurology, Muenster University Hospital, Münster, Germany.
  • Becker M; Labor Becker & Kollegen, Munich, Germany.
  • Hohenfellner K; RoMed Klinikum Rosenheim, Department of Pedriatric Nephrology, Rosenheim, Germany.
  • Müller-Felber W; Department of Pediatric Neurology and Developmental Medicine, Dr. v. Hauner Children's Hospital, LMU - University of Munich, Munich, Germany.
J Neuromuscul Dis ; 6(4): 503-515, 2019.
Article em En | MEDLINE | ID: mdl-31594245

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Atrofias Musculares Espinais da Infância / Deleção de Sequência / Doenças Neurodegenerativas Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Limite: Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: J Neuromuscul Dis Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Atrofias Musculares Espinais da Infância / Deleção de Sequência / Doenças Neurodegenerativas Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Limite: Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: J Neuromuscul Dis Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Holanda