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Experienced complaints, activity limitations and loss of motor capacities in patients with pure hereditary spastic paraplegia: a web-based survey in the Netherlands.
van Lith, Bas J H; Kerstens, Hans C J W; van den Bemd, Laura A C; der Sanden, Maria W G Nijhuis-van; Weerdesteyn, Vivian; Smeets, Rob J E M; Fheodoroff, Klemens; van de Warrenburg, Bart P C; Geurts, Alexander C H.
Afiliación
  • van Lith BJH; Department of Rehabilitation, Donders Institute for Brain, Cognition and Behaviour, Radboud university medical center, PO Box 9101, 6500, HB, Nijmegen, The Netherlands. Bas.vanLith@Radboudumc.nl.
  • Kerstens HCJW; HAN University of Applied Sciences, PO Box 6960, 6503, GL, Nijmegen, The Netherlands.
  • van den Bemd LAC; Radboud Institute for Health Sciences, Scientific Institute for Quality of Healthcare, Radboud university medical center, PO Box 9101, 6500, HB, Nijmegen, The Netherlands.
  • der Sanden MWGN; Department of Rehabilitation, Sint Maartenskliniek, PO Box 9011, 6500, GM, Nijmegen, The Netherlands.
  • Weerdesteyn V; Radboud Institute for Health Sciences, Scientific Institute for Quality of Healthcare, Radboud university medical center, PO Box 9101, 6500, HB, Nijmegen, The Netherlands.
  • Smeets RJEM; Department of Rehabilitation, Donders Institute for Brain, Cognition and Behaviour, Radboud university medical center, PO Box 9101, 6500, HB, Nijmegen, The Netherlands.
  • Fheodoroff K; Department of Rehabilitation Medicine, Maastricht University, Research School CAPHRI, PO Box 616, 6200, MD, Maastricht, the Netherlands.
  • van de Warrenburg BPC; Gailtal-Klinik, Radnigerstrasse 12, 9620, Hermagor, Austria.
  • Geurts ACH; Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud university medical center, PO Box 9101, 6500, HB, Nijmegen, The Netherlands.
Orphanet J Rare Dis ; 15(1): 64, 2020 03 04.
Article en En | MEDLINE | ID: mdl-32131864
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos