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Newborn screening for spinal muscular atrophy in Germany: clinical results after 2 years.

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Title: Newborn screening for spinal muscular atrophy in Germany: clinical results after 2 years.
Authors: Vill K; Dr. v. Hauner Children's Hospital, Department of Pediatric Neurology and Developmental Medicine, LMU - University of Munich, Lindwurmstraße 4, 80337, München, Germany., Schwartz O; Department of Pediatric Neurology, Münster University Hospital, Münster, Germany., Blaschek A; Dr. v. Hauner Children's Hospital, Department of Pediatric Neurology and Developmental Medicine, LMU - University of Munich, Lindwurmstraße 4, 80337, München, Germany., Gläser D; Center for Human Genetics, Genetikum®, Neu-Ulm, Germany., Nennstiel U; Screening Center of the Bavarian Health and Food Safety Authority, Oberschleißheim, Germany., Wirth B; Institute of Human Genetics, Center for Molecular Genetics Cologne and Center for Rare Diseases, University of Cologne, Cologne, Germany., Burggraf S; Labor Becker und Kollegen, Munich, Germany., Röschinger W; Labor Becker und Kollegen, Munich, Germany., Becker M; Labor Becker und Kollegen, Munich, Germany., Czibere L; Labor Becker und Kollegen, Munich, Germany., Durner J; Labor Becker und Kollegen, Munich, Germany.; Department of Operative/Restorative Dentistry, Periodontology and Pedodontics, LMU - University of Munich, München, Germany., Eggermann K; Institute of Human Genetics, Medical Faculty, RWTH Aachen University, Aachen, Germany., Olgemöller B; Formerly Labor Becker, Olgemöller und Kollegen, Munich, Germany., Harms E; Department of Pediatrics, Muenster University Hospital, Münster, Germany., Schara U; Department of Pediatric Neurology, Developmental Neurology and Social Pediatrics, University of Essen, Essen, Germany., Kölbel H; Department of Pediatric Neurology, Developmental Neurology and Social Pediatrics, University of Essen, Essen, Germany., Müller-Felber W; Dr. v. Hauner Children's Hospital, Department of Pediatric Neurology and Developmental Medicine, LMU - University of Munich, Lindwurmstraße 4, 80337, München, Germany. Wolfgang.mueller-felber@med.uni-muenchen.de.
Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2021 Mar 31; Vol. 16 (1), pp. 153. Date of Electronic Publication: 2021 Mar 31.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Newborn screening for spinal muscular atrophy in Germany: clinical results after 2 years.
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  Data: <searchLink fieldCode="AU" term="%22Vill+K%22">Vill K</searchLink>; Dr. v. Hauner Children's Hospital, Department of Pediatric Neurology and Developmental Medicine, LMU - University of Munich, Lindwurmstraße 4, 80337, München, Germany.<br /><searchLink fieldCode="AU" term="%22Schwartz+O%22">Schwartz O</searchLink>; Department of Pediatric Neurology, Münster University Hospital, Münster, Germany.<br /><searchLink fieldCode="AU" term="%22Blaschek+A%22">Blaschek A</searchLink>; Dr. v. Hauner Children's Hospital, Department of Pediatric Neurology and Developmental Medicine, LMU - University of Munich, Lindwurmstraße 4, 80337, München, Germany.<br /><searchLink fieldCode="AU" term="%22Gläser+D%22">Gläser D</searchLink>; Center for Human Genetics, Genetikum®, Neu-Ulm, Germany.<br /><searchLink fieldCode="AU" term="%22Nennstiel+U%22">Nennstiel U</searchLink>; Screening Center of the Bavarian Health and Food Safety Authority, Oberschleißheim, Germany.<br /><searchLink fieldCode="AU" term="%22Wirth+B%22">Wirth B</searchLink>; Institute of Human Genetics, Center for Molecular Genetics Cologne and Center for Rare Diseases, University of Cologne, Cologne, Germany.<br /><searchLink fieldCode="AU" term="%22Burggraf+S%22">Burggraf S</searchLink>; Labor Becker und Kollegen, Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Röschinger+W%22">Röschinger W</searchLink>; Labor Becker und Kollegen, Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Becker+M%22">Becker M</searchLink>; Labor Becker und Kollegen, Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Czibere+L%22">Czibere L</searchLink>; Labor Becker und Kollegen, Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Durner+J%22">Durner J</searchLink>; Labor Becker und Kollegen, Munich, Germany.; Department of Operative/Restorative Dentistry, Periodontology and Pedodontics, LMU - University of Munich, München, Germany.<br /><searchLink fieldCode="AU" term="%22Eggermann+K%22">Eggermann K</searchLink>; Institute of Human Genetics, Medical Faculty, RWTH Aachen University, Aachen, Germany.<br /><searchLink fieldCode="AU" term="%22Olgemöller+B%22">Olgemöller B</searchLink>; Formerly Labor Becker, Olgemöller und Kollegen, Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Harms+E%22">Harms E</searchLink>; Department of Pediatrics, Muenster University Hospital, Münster, Germany.<br /><searchLink fieldCode="AU" term="%22Schara+U%22">Schara U</searchLink>; Department of Pediatric Neurology, Developmental Neurology and Social Pediatrics, University of Essen, Essen, Germany.<br /><searchLink fieldCode="AU" term="%22Kölbel+H%22">Kölbel H</searchLink>; Department of Pediatric Neurology, Developmental Neurology and Social Pediatrics, University of Essen, Essen, Germany.<br /><searchLink fieldCode="AU" term="%22Müller-Felber+W%22">Müller-Felber W</searchLink>; Dr. v. Hauner Children's Hospital, Department of Pediatric Neurology and Developmental Medicine, LMU - University of Munich, Lindwurmstraße 4, 80337, München, Germany. Wolfgang.mueller-felber@med.uni-muenchen.de.
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  Data: <searchLink fieldCode="JN" term="%22101266602%22">Orphanet journal of rare diseases</searchLink> [Orphanet J Rare Dis] 2021 Mar 31; Vol. 16 (1), pp. 153. <i>Date of Electronic Publication: </i>2021 Mar 31.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101266602 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1750-1172 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217501172%22">17501172 </searchLink><i>NLM ISO Abbreviation: </i>Orphanet J Rare Dis <i>Subsets: </i>MEDLINE
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