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Twenty years of molecular analyses in amyotrophic lateral sclerosis: genetic landscape of Italian patients.
Lamp, Merit; Origone, Paola; Geroldi, Alessandro; Verdiani, Simonetta; Gotta, Fabio; Caponnetto, Claudia; Devigili, Grazia; Verriello, Lorenzo; Scialò, Carlo; Cabona, Corrado; Canosa, Antonio; Vanni, Irene; Bellone, Emilia; Eleopra, Roberto; Mandich, Paola.
Afiliação
  • Lamp M; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, Section of Medical Genetics, University of Genoa, Genoa, Italy; Medical Genetics Unit, Department of Diagnosis, Pathology and Treatments of High Technological Complexity, IRCCS Ospedale Policlinico San M
  • Origone P; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, Section of Medical Genetics, University of Genoa, Genoa, Italy; Medical Genetics Unit, Department of Diagnosis, Pathology and Treatments of High Technological Complexity, IRCCS Ospedale Policlinico San M
  • Geroldi A; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, Section of Medical Genetics, University of Genoa, Genoa, Italy.
  • Verdiani S; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, Section of Medical Genetics, University of Genoa, Genoa, Italy.
  • Gotta F; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, Section of Medical Genetics, University of Genoa, Genoa, Italy; Medical Genetics Unit, Department of Diagnosis, Pathology and Treatments of High Technological Complexity, IRCCS Ospedale Policlinico San M
  • Caponnetto C; Neurology Unit, Department of Neurosciences and Sense Organs, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
  • Devigili G; 1st Neurology Unit, Department of Clinical Neurosciences, IRCCS "CarloBesta" Neurological Institute, Milan, Italy.
  • Verriello L; Neurology Unit, Department of Neurosciences, University Hospital "Santa Maria della Misericordia", Udine, Italy.
  • Scialò C; Neurology Unit, Department of Neurosciences and Sense Organs, IRCCS Ospedale Policlinico San Martino, Genoa, Italy; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, Neurology Unit, University of Genoa, Genoa, Italy.
  • Cabona C; Neurology Unit, Department of Neurosciences and Sense Organs, IRCCS Ospedale Policlinico San Martino, Genoa, Italy; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, Neurology Unit, University of Genoa, Genoa, Italy.
  • Canosa A; Neurology Unit, Department of Neurosciences and Sense Organs, IRCCS Ospedale Policlinico San Martino, Genoa, Italy; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, Neurology Unit, University of Genoa, Genoa, Italy.
  • Vanni I; Lung Cancer Unit, Department of Integrated Oncological Therapies, IRCCS Ospedale Policlinico SanMartino, Genoa, Italy.
  • Bellone E; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, Section of Medical Genetics, University of Genoa, Genoa, Italy; Medical Genetics Unit, Department of Diagnosis, Pathology and Treatments of High Technological Complexity, IRCCS Ospedale Policlinico San M
  • Eleopra R; 1st Neurology Unit, Department of Clinical Neurosciences, IRCCS "CarloBesta" Neurological Institute, Milan, Italy.
  • Mandich P; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, Section of Medical Genetics, University of Genoa, Genoa, Italy; Medical Genetics Unit, Department of Diagnosis, Pathology and Treatments of High Technological Complexity, IRCCS Ospedale Policlinico San M
Neurobiol Aging ; 66: 179.e5-179.e16, 2018 06.
Article em En | MEDLINE | ID: mdl-29525178
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estudos de Associação Genética / Sequenciamento de Nucleotídeos em Larga Escala / Esclerose Lateral Amiotrófica / Mutação Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Neurobiol Aging Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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XML
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estudos de Associação Genética / Sequenciamento de Nucleotídeos em Larga Escala / Esclerose Lateral Amiotrófica / Mutação Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Neurobiol Aging Ano de publicação: 2018 Tipo de documento: Article