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Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease.
Di Donato, Ilaria; Bianchi, Silvia; Gallus, Gian Nicola; Cerase, Alfonso; Taglia, Ilaria; Pescini, Francesca; Nannucci, Serena; Battisti, Carla; Inzitari, Domenico; Pantoni, Leonardo; Zini, Andrea; Federico, Antonio; Dotti, Maria Teresa.
Afiliación
  • Di Donato I; Department of Medicine, Surgery and Neurosciences, Medical School, University of Siena, Siena, Italy.
  • Bianchi S; Department of Medicine, Surgery and Neurosciences, Medical School, University of Siena, Siena, Italy.
  • Gallus GN; Department of Medicine, Surgery and Neurosciences, Medical School, University of Siena, Siena, Italy.
  • Cerase A; Unit NINT Neuroimaging and Neurointervention, Department of Neurological and Sensorineural Sciences, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
  • Taglia I; Department of Medicine, Surgery and Neurosciences, Medical School, University of Siena, Siena, Italy.
  • Pescini F; NEUROFARBA Department, Neuroscience section, University of Florence, Florence, Italy.
  • Nannucci S; NEUROFARBA Department, Neuroscience section, University of Florence, Florence, Italy.
  • Battisti C; Department of Medicine, Surgery and Neurosciences, Medical School, University of Siena, Siena, Italy.
  • Inzitari D; NEUROFARBA Department, Neuroscience section, University of Florence, Florence, Italy.
  • Pantoni L; NEUROFARBA Department, Neuroscience section, University of Florence, Florence, Italy.
  • Zini A; Stroke Unit, Neurology Clinic, Department of Neuroscience, Nuovo Ospedale Civile S. Agostino-Estense, University Hospital of Modena, Modena, Italy.
  • Federico A; Department of Medicine, Surgery and Neurosciences, Medical School, University of Siena, Siena, Italy.
  • Dotti MT; Department of Medicine, Surgery and Neurosciences, Medical School, University of Siena, Siena, Italy.
CNS Neurosci Ther ; 23(9): 759-765, 2017 Sep.
Article en En | MEDLINE | ID: mdl-28782182
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Salud de la Familia / Enfermedades de los Pequeños Vasos Cerebrales / Serina Peptidasa A1 que Requiere Temperaturas Altas / Mutación Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: CNS Neurosci Ther Asunto de la revista: NEUROLOGIA / TERAPEUTICA Año: 2017 Tipo del documento: Article País de afiliación: Italia
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Salud de la Familia / Enfermedades de los Pequeños Vasos Cerebrales / Serina Peptidasa A1 que Requiere Temperaturas Altas / Mutación Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: CNS Neurosci Ther Asunto de la revista: NEUROLOGIA / TERAPEUTICA Año: 2017 Tipo del documento: Article País de afiliación: Italia