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Low prevalence of known pathogenic mutations in dominant PD genes: A Swedish multicenter study.
Puschmann, Andreas; Jiménez-Ferrer, Itzia; Lundblad-Andersson, Elin; Mårtensson, Emma; Hansson, Oskar; Odin, Per; Widner, Håkan; Brolin, Kajsa; Mzezewa, Ropafadzo; Kristensen, Jonas; Soller, Maria; Rödström, Emil Ygland; Ross, Owen A; Toft, Mathias; Breedveld, Guido J; Bonifati, Vincenzo; Brodin, Lovisa; Zettergren, Anna; Sydow, Olof; Linder, Jan; Wirdefeldt, Karin; Svenningsson, Per; Nissbrandt, Hans; Belin, Andrea Carmine; Forsgren, Lars; Swanberg, Maria.
Afiliação
  • Puschmann A; Lund University, Skåne University Hospital, Department of Clinical Sciences Lund, Neurology, Lund, Sweden. Electronic address: Andreas.Puschmann@med.lu.se.
  • Jiménez-Ferrer I; Lund University, Department of Experimental Medical Science, Lund, Sweden.
  • Lundblad-Andersson E; Department of Clinical Genetics and Pathology, Division of Laboratory Medicine, Office for Medical Services, Region Skåne, Sweden.
  • Mårtensson E; Department of Clinical Genetics and Pathology, Division of Laboratory Medicine, Office for Medical Services, Region Skåne, Sweden.
  • Hansson O; Clinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Sweden; Memory Clinic, Skåne University Hospital, Malmö, Sweden.
  • Odin P; Lund University, Skåne University Hospital, Department of Clinical Sciences Lund, Neurology, Lund, Sweden.
  • Widner H; Lund University, Skåne University Hospital, Department of Clinical Sciences Lund, Neurology, Lund, Sweden.
  • Brolin K; Lund University, Department of Experimental Medical Science, Lund, Sweden.
  • Mzezewa R; Lund University, Department of Experimental Medical Science, Lund, Sweden.
  • Kristensen J; Department of Clinical Genetics and Pathology, Division of Laboratory Medicine, Office for Medical Services, Region Skåne, Sweden.
  • Soller M; Department of Clinical Genetics and Pathology, Division of Laboratory Medicine, Office for Medical Services, Region Skåne, Sweden.
  • Rödström EY; Lund University, Skåne University Hospital, Department of Clinical Sciences Lund, Neurology, Lund, Sweden.
  • Ross OA; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, 32224, USA.
  • Toft M; Department of Neurology, Oslo University Hospital, Oslo, Norway.
  • Breedveld GJ; Erasmus MC, University Medical Center Rotterdam, Department of Clinical Genetics, Rotterdam, The Netherlands.
  • Bonifati V; Erasmus MC, University Medical Center Rotterdam, Department of Clinical Genetics, Rotterdam, The Netherlands.
  • Brodin L; Department of Clinical Neuroscience, Karolinska University Hospital, Stockholm, Sweden.
  • Zettergren A; Department of Psychiatry and Neurochemistry, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Sydow O; Department of Clinical Neuroscience, Karolinska University Hospital, Stockholm, Sweden.
  • Linder J; Department of Pharmacology and Clinical Neuroscience, Umeå University, Umeå, Sweden.
  • Wirdefeldt K; Department of Clinical Neuroscience, Karolinska University Hospital, Stockholm, Sweden; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Svenningsson P; Department of Clinical Neuroscience, Karolinska University Hospital, Stockholm, Sweden.
  • Nissbrandt H; Department of Psychiatry and Neurochemistry, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Belin AC; Department of Neuroscience, Karolinska Institutet, Solna, Sweden.
  • Forsgren L; Department of Pharmacology and Clinical Neuroscience, Umeå University, Umeå, Sweden.
  • Swanberg M; Lund University, Department of Experimental Medical Science, Lund, Sweden.
Parkinsonism Relat Disord ; 66: 158-165, 2019 09.
Article em En | MEDLINE | ID: mdl-31422003
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Predisposição Genética para Doença Tipo de estudo: Clinical_trials / Prevalence_studies / Risk_factors_studies Limite: Humans País/Região como assunto: Europa Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Predisposição Genética para Doença Tipo de estudo: Clinical_trials / Prevalence_studies / Risk_factors_studies Limite: Humans País/Região como assunto: Europa Idioma: En Ano de publicação: 2019 Tipo de documento: Article