Zobrazeno 1 - 10
of 127
pro vyhledávání: '"Gutiérrez-Molina M"'
Autor:
Pascual-Castroviejo, I., Hernández-Moneo, J.L., Pascual-Pascual, S.I., Viaño, J., Gutiérrez-Molina, M., Velazquez-Fragua, R., Quiñones Tapia, D., Morales Bastos, C.
Publikováno v:
In Neurología (English Edition) November-December 2013 28(9):550-557
Autor:
Pascual-Castroviejo, I., Hernández-Moneo, J.L., Pascual-Pascual, S.I., Viaño, J., Gutiérrez-Molina, M., Velazquez-Fragua, R., Quiñones Tapia, D., Morales Bastos, C.
Publikováno v:
In Neurología November-December 2013 28(9):550-557
Autor:
Pascual-Castroviejo, I., Pascual-Pascual, S.I., Velázquez-Fragua, R., Viaño, J., Carceller, F., Hernández-Moneo, J.L., Gutiérrez-Molina, M., Morales, C.
Publikováno v:
In Neurología (English Edition) 2010 25(5):314-321
Autor:
Pascual-Castroviejo, I., Pascual-Pascual, S.I., Velázquez-Fragua, R., Viaño, J., Carceller, F., Hernández-Moneo, J.L., Gutiérrez-Molina, M., Morales, C.
Publikováno v:
In Neurología 2010 25(5):314-321
Autor:
Saceda-Gutiérrez, J.M., Isla-Guerrero, A.J., Pérez-López, C., Ortega-Martínez, R., Gómez de la Riva, A., Gandia-González, M.L., Gutiérrez-Molina, M., Rey-Herranz, J.A.
Publikováno v:
In Neurocirugía 2007 18(6):496-504
Autor:
Ríos Blanco, J.J., Gómez Cerezo, J., Suárez García, I., Vázquez Rodríguez, J.J., Barbado Hernández, F.J., Gutiérrez Molina, M.
Publikováno v:
In Revista clinica espanola November 2000 200(11):597-601
Autor:
Pascual-Castroviejo, I., Van Der Knaap, M. S., Pronk, J. C., García-Segura, J. M., Gutiérrez-Molina, M., Pascual-Pascual, S. I.
Publikováno v:
Pascual-Castroviejo, I, Van Der Knaap, M S, Pronk, J C, García-Segura, J M, Gutiérrez-Molina, M & Pascual-Pascual, S I 2005, ' Vacuolating megalencephalic leukoencephalopathy : 24 Year follow-up of two siblings ', Neurologia, vol. 20, no. 1, pp. 33-40 .
Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is an autosomal recessive disorder with a chronic progressive course. The gene, MLC1, has been localized on chromosome 22qtell and 26 different mutations have been described. We report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10172::e6123eab8d6e7830216d4c5d7887ebd8
https://research.vumc.nl/en/publications/81a88a7c-0670-4c63-a3f2-5427fc14f87f
https://research.vumc.nl/en/publications/81a88a7c-0670-4c63-a3f2-5427fc14f87f
Autor:
Martínez-Bermejo A, López-Martín V, Jose Serratosa, Gutiérrez-Molina M, Gómez-Garre P, Arcas J, Tendero A, Roche C, Pérez-Mies B
Publikováno v:
Europe PubMed Central
Lafora s disease is a type of progressive myoclonic epilepsy with bad prognosis. Until now diagnosis was based on finding characteristic intracytoplasmatic polyglucosan bodies in biopsies of sweat secreting cells in the skin. Recently the gene respon
Autor:
Arpa J, Javier Garcia-Planells, Soler R, Cruz Martínez A, Mj, Sarriá Lucas, López-Pajares R, Gutiérrez Molina M, Santiago S, Palau A, Palau F
Publikováno v:
Europe PubMed Central
ResearcherID
ResearcherID
We have carried out electrophysiological studies and sural nerve biopsy evaluation in a Spanish family with genetically proven Machado-Joseph disease (SCA3/MJD) phenotype III.Two symptomatic and other two asymptomatic members of the family were clini
Autor:
Javier Arpa, Gutiérrez-Molina M, Tatay J, Yolanda Campos, Pérez-Conde Mc, Lacasa T, Martin-Casanueva Ma, Joaquín Arenas, Cruz-Martínez A, Barreiro P, López-Pajares R, Morales Mc
Publikováno v:
Scopus-Elsevier
Objectives - We analyzed the percentage of mitochondrial DNA (mtDNA) heteroplasmy in blood samples of 13 individuals belonging to a three family generation of myoclonic epilepsy with ragged-red fibers (MERRF) and compared the 5 affected patients and