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Reply to: "Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion".
De la Casa-Fages, Beatriz; Fernández-Eulate, Gorka; Gamez, Josep; Barahona-Hernando, Raúl; Morís, Germán; García-Barcina, María; Infante, Jon; Zulaica, Miren; Fernández-Pelayo, Uxoa; Muñoz-Oreja, Mikel; Urtasun, Miguel; Olaskoaga, Ander; Zelaya, Victoria; Jericó, Ivonne; Saez-Villaverde, Raquel; Catalina, Irene; Sola, Emma; Martínez-Sáez, Elena; Pujol, Aurora; Ruiz, Montserrat; Schlüter, Agatha; Spinazzola, Antonella; Muñoz-Blanco, Jose Luis; Grandas, Francisco; Holt, Ian; Álvarez, Victoria; López de Munaín, Adolfo.
Afiliação
  • De la Casa-Fages B; Department of Neurology, Hospital General Universitario Gregorio Marañon, Madrid, Spain.
  • Fernández-Eulate G; Movement Disorders Unit, National Referral Center for Rare Diseases with Movement Disorders, Hospital General Universitario Gregorio Marañon, Madrid, Spain.
  • Gamez J; Neurosciences Area, Instituto Investigacion Sanitaria Gregorio Marañon, Madrid, Spain.
  • Barahona-Hernando R; Department of Neurology, Hospital Universitario Donostia, San Sebastian, Spain.
  • Morís G; Department of Neurosciences, Instituto Biodonostia, San Sebastian, Spain.
  • García-Barcina M; Department of Neurology, Hospital General Universitari Vall d'Hebron-Universitat Autònoma de Barcelona-Vall d'Hebron Research Institute (UAB-VHIR), Barcelona, Spain.
  • Infante J; European Reference Network on Rare Neurological Diseases, Hospital General Universitari Vall d'Hebron-UAB, Barcelona, Spain.
  • Zulaica M; Department of Neurology, Hospital General Universitario Gregorio Marañon, Madrid, Spain.
  • Fernández-Pelayo U; Amyotrophic Lateral Sclerosis (ALS)-Neuromuscular Unit, Hospital General Universitario Gregorio Marañon, Madrid, Spain.
  • Muñoz-Oreja M; Department of Neurology, Hospital Ruber Juan Bravo, Grupo Quironsalud, Madrid, Spain.
  • Urtasun M; Instituto de Investigación Biosanitaria del Principado de Asturias, Oviedo, Spain.
  • Olaskoaga A; Department of Neurology, Hospital Universitario Central de Asturias, Oviedo, Spain.
  • Zelaya V; Genetics Unit, Hospital Universitario Basurto, Bilbao, Spain.
  • Jericó I; Department of Neurology, Hospital Universitario Marques de Valdecilla-Instituto de Investigación Marqués de Valdecilla (IDIVAL), University of Cantabria, Santander, Spain.
  • Saez-Villaverde R; Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas, Institute Carlos III, Santander, Spain.
  • Catalina I; Department of Neurosciences, Instituto Biodonostia, San Sebastian, Spain.
  • Sola E; Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas, Institute Carlos III, Santander, Spain.
  • Martínez-Sáez E; Department of Neurosciences, Instituto Biodonostia, San Sebastian, Spain.
  • Pujol A; Department of Neurosciences, Instituto Biodonostia, San Sebastian, Spain.
  • Ruiz M; Department of Neurology, Hospital Universitario Donostia, San Sebastian, Spain.
  • Schlüter A; Hospital de Zumarraga, Zumarraga, Spain.
  • Spinazzola A; Department of Pathology, Complejo Hospitalario de Navarra, Pamplona, Spain.
  • Muñoz-Blanco JL; Department of Neurology, Complejo Hospitalario de Navarra, Pamplona, Spain.
  • Grandas F; Department of Genetics, Hospital Universitario Donostia, San Sebastian, Spain.
  • Holt I; Department of Neurology, Hospital General Universitario Gregorio Marañon, Madrid, Spain.
  • Álvarez V; Amyotrophic Lateral Sclerosis (ALS)-Neuromuscular Unit, Hospital General Universitario Gregorio Marañon, Madrid, Spain.
  • López de Munaín A; Department of Pathology, Hospital General Universitario Gregorio Maranon, Madrid, Spain.
Mov Disord ; 34(12): 1932-1933, 2019 12.
Article em En | MEDLINE | ID: mdl-31845766
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Transtornos Parkinsonianos Limite: Humans Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Espanha
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Transtornos Parkinsonianos Limite: Humans Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Espanha