Genome sequencing uncovers phenocopies in primary progressive multiple sclerosis.

Jia, Xiaoming; Madireddy, Lohith; Caillier, Stacy; Santaniello, Adam; Esposito, Federica; Comi, Giancarlo; Stuve, Olaf; Zhou, Yuan; Taylor, Bruce; Kilpatrick, Trevor; Martinelli-Boneschi, Filippo; Cree, Bruce A C; Oksenberg, Jorge R; Hauser, Stephen L; Baranzini, Sergio E

Jia, Xiaoming; Madireddy, Lohith; Caillier, Stacy; Santaniello, Adam; Esposito, Federica; Comi, Giancarlo; Stuve, Olaf; Zhou, Yuan; Taylor, Bruce; Kilpatrick, Trevor; Martinelli-Boneschi, Filippo; Cree, Bruce A C; Oksenberg, Jorge R; Hauser, Stephen L; Baranzini, Sergio E.

Afiliación

Jia X; UCSF Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA.
Madireddy L; Department of Neurology, University of California San Francisco, San Francisco, CA.
Caillier S; UCSF Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA.
Santaniello A; Department of Neurology, University of California San Francisco, San Francisco, CA.
Esposito F; UCSF Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA.
Comi G; Department of Neurology, University of California San Francisco, San Francisco, CA.
Stuve O; UCSF Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA.
Zhou Y; Department of Neurology, University of California San Francisco, San Francisco, CA.
Taylor B; Laboratory of Human Genetics of Neurological Disorders, Institute of Experimental Neurology (INSpe), Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy.
Kilpatrick T; Department of Neurology and Neuro-rehabilitation, San Raffaele Scientific Institute, Milan, Italy.
Martinelli-Boneschi F; Laboratory of Human Genetics of Neurological Disorders, Institute of Experimental Neurology (INSpe), Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy.
Cree BAC; Department of Neurology and Neuro-rehabilitation, San Raffaele Scientific Institute, Milan, Italy.
Oksenberg JR; Department of Neurology and Neurotherapeutics, University of Texas Southwestern Medical, Dallas, TX.
Hauser SL; Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.
Baranzini SE; Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.

Ann Neurol ; 84(1): 51-63, 2018 07.

Article en En | MEDLINE | ID: mdl-29908077

Asunto(s)

Estudio de Asociación del Genoma Completo; Esclerosis Múltiple Crónica Progresiva/genética; Esclerosis Múltiple Crónica Progresiva/fisiopatología; Mutación/genética; Adolescente; Adulto; Anciano; Niño; Preescolar; Estudios de Cohortes; Quistes/genética; Femenino; Genotipo; Enfermedades Desmielinizantes del Sistema Nervioso Central Hereditarias/genética; Humanos; Cinesinas; Masculino; Proteínas de la Membrana/genética; Proteínas de Transporte de Membrana/genética; Metaanálisis como Asunto; Persona de Mediana Edad; Paraplejía/genética; Fenotipo; Adulto Joven

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Esclerosis Múltiple Crónica Progresiva / Estudio de Asociación del Genoma Completo / Mutación Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Neurol Año: 2018 Tipo del documento: Article País de afiliación: Canadá

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google