Navegar por autor "García Murias, María"

Mostrando ítems 1-7 de 7

A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy

2011- San Millan Tejado, Beatriz; Carracedo Álvarez, Ángel; Sobrido Gómez, María Jesús; Blanco Arias, Patricia; García Murias, María; [et al.]
'Costa da Morte' ataxia is spinocerebellar ataxia 36: Clinical and genetic characterization

2012- Carracedo Álvarez, Ángel; Sobrido Gómez, María Jesús; Blanco Arias, Patricia; García Murias, María; Quintans Castro, Beatriz; [et al.]
First SCA36 patients in Europe: Clinical, physiological and imaging details of 10 families

2012- Carracedo Álvarez, Ángel; Sobrido Gómez, María Jesús; Blanco Arias, Patricia; Cacheiro Martínez, Pilar; García Murias, María; [et al.]
Molecular Basis, Diagnostic Challenges and Therapeutic Approaches of Alport Syndrome: A Primer for Clinicians

2021- MartInez Pulleiro, Raquel; García Murias, María; Fidalgo Díaz, Manuel; García González , Miguel Ángel
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice

2013- Carracedo Álvarez, Ángel; Sobrido Gómez, María Jesús; García Murias, María; Prieto González, José María; Ordoñez Ugalde, Andrés [et al.]
Neuropsychological assessment in SCA36: 'Costa da Morte' ataxia

2014- Pumar Cebreiro, José Manuel; Carracedo Álvarez, Ángel; Labella Caballero, Torcuato; Sobrido Gómez, María Jesús; Fernández Prieto, Montserrat; [et al.]
Neuropsychological assessment in SCA36: 'Costa da Morte' ataxia

2014- Pumar Cebreiro, José Manuel; Carracedo Álvarez, Ángel; Sobrido Gómez, María Jesús; Fernández Prieto, Montserrat; Pardo Pérez, María; [et al.]