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Increased chitotriosidase 1 concentration following nusinersen treatment in spinal muscular atrophy.
Freigang, Maren; Steinacker, Petra; Wurster, Claudia Diana; Schreiber-Katz, Olivia; Osmanovic, Alma; Petri, Susanne; Koch, Jan Christoph; Rostásy, Kevin; Falkenburger, Björn; Ludolph, Albert Christian; Otto, Markus; Hermann, Andreas; Günther, René.
Afiliación
  • Freigang M; Department of Neurology, Technische Universität Dresden, Dresden, Germany.
  • Steinacker P; Department of Neurology, Ulm University, Ulm, Germany.
  • Wurster CD; Department of Neurology, Ulm University, Ulm, Germany.
  • Schreiber-Katz O; Department of Neurology, Hannover Medical School, Hannover, Germany.
  • Osmanovic A; Department of Neurology, Hannover Medical School, Hannover, Germany.
  • Petri S; Department of Neurology, Hannover Medical School, Hannover, Germany.
  • Koch JC; Department of Neurology, University Medicine Göttingen, Göttingen, Germany.
  • Rostásy K; Department of Pediatric Neurology, Children's Hospital Datteln, University Witten/Herdecke, Datteln, Germany.
  • Falkenburger B; Department of Neurology, Technische Universität Dresden, Dresden, Germany.
  • Ludolph AC; German Center for Neurodegenerative Diseases (DZNE) Dresden, Dresden, Germany.
  • Otto M; Department of Neurology, Ulm University, Ulm, Germany.
  • Hermann A; German Center for Neurodegenerative Diseases (DZNE) Ulm, Ulm, Germany.
  • Günther R; Department of Neurology, Ulm University, Ulm, Germany.
Orphanet J Rare Dis ; 16(1): 330, 2021 07 28.
Article en En | MEDLINE | ID: mdl-34321067
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oligonucleótidos / Atrofia Muscular Espinal Tipo de estudio: Clinical_trials / Observational_studies Límite: Adult / Child / Humans Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2021 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oligonucleótidos / Atrofia Muscular Espinal Tipo de estudio: Clinical_trials / Observational_studies Límite: Adult / Child / Humans Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2021 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido