Zobrazeno 1 - 10
of 23
pro vyhledávání: '"E., Martínez Góngora"'
Autor:
Carola Seifried, Sánchez-Cruz G, Luis Velázquez-Pérez, E Martínez-Góngora, S Stuckrad-Barre, Ulf Ziemann, Michael Fetter, Georg Auburger, N. Santos-Falcón, B. Viebahn, M. Abele, Ruth Pérez-González, L. Almaguer, Thomas Klockgether, Mercedes Velázquez-Manresa, Nalia Canales
Publikováno v:
Annals of the New York Academy of Sciences. 1039:524-527
We measured in 82 spinocerebellar ataxia type 2 (SCA2) patients and in 80 controls maximal saccade velocity (MSV) and correlated it to polyglutamine expansion size and disease duration. MSV is strongly decreased in SCA2 patients and is influenced mos
Autor:
Carola Seifried, Michael Fetter, Bettina Viebahn, Sánchez-Cruz G, E Martínez-Góngora, Ulf Ziemann, M. Abele, Nalia Canales, Luis Enrique Almaguer, N. Santos-Falcón, Luis Velázquez-Pérez, Mercedes Velázquez-Manresa, Georg Auburger, Ruth Pérez-González, Thomas Klockgether, Sebastian von Stuckrad-Barre
Publikováno v:
Annals of Neurology. 56:444-447
We assessed maximal saccade velocity (MSV) in 82 spinocerebellar ataxia type 2 (SCA2) patients and 80 controls, correlating it to disease duration, polyglutamine expansion size, age at onset, ataxia score, age, and sex. Little overlap with normal val
Autor:
M Paneque Herrera, L Velásquez Pérez, CL Proenza, D. Cuello Almarales, N. Santos Falcón, K Escalona Batallán, Y Rodríguez Almira, E Martínez Góngora, L.E. Almaguer Mederos
Publikováno v:
Clinical Genetics. 74:571-573
Autor:
Ruth Pérez-González, Juan Fernandez-Ruiz, René Drucker-Colín, Yaquelín Medrano, E Martínez-Góngora, Georg Auburger, Luis E. Almaguer-Mederos, Rosalinda Diaz, Luis Velásquez-Perez, Carola Seifried, Nalia Canales, Sánchez-Cruz G
Publikováno v:
Neuropsychologia. 45(12)
Patients with spinocerebellar ataxia type 2 (SCA2), develop severe pontine nuclei, inferior olives, and Purkinje cell degeneration. This form of autosomal dominant cerebellar ataxia is accompanied by progressive ataxia and dysarthria. Although the mo
Autor:
I, Pérez-Avila, J A, Fernández-Vieitez, E, Martínez-Góngora, R, Ochoa-Mastrapa, M G, Velázquez-Manresa
Publikováno v:
Revista de neurologia. 39(10)
Type 2 spinocerebelar ataxia (SCA2) is a neurodegenerative disease with higher prevalence and incidence in Holguín province, Cuba. At present, there is not any drug to counteract the loss of coordinative motor capacities of these patients. Thus phys
Autor:
G, Sánchez-Cruz, L, Velázquez-Pérez, L, Gómez-Peña, E, Martínez-Góngora, G, Castellano-Sánchez, N, Santos-Falcón
Publikováno v:
Revista de neurologia. 33(5)
Dysautonomic features are the clinical signs and symptoms derived from anomalous functioning of the sympathetic or parasympathetic nervous systems in either the peripheral or central parts.To identify the clinical features related to dysautonomia in
Autor:
E Martínez-Góngora, I Pérez-Avila, J A Fernández-Vieitez, R Ochoa-Mastrapa, M G Velázquez-Manresa
Publikováno v:
Revista de Neurología. 39:907
Introduccion. La ataxia espinocerebelosa tipo 2 (SCA2) es una enfermedad neurodegenerativa con una alta prevalencia e incidencia en la provincia de Holguin, Cuba. Hasta ahora no se cuenta con ningun medicamento capaz de contrarrestar la perdida de la
Autor:
E Martínez-Góngora, de la Hoz-Oliveras J, Julio Cesar Rodríguez-Díaz, Sánchez-Cruz G, Paneque-Herrera M, N. Santos-Falcón, Herrera-Dominguez H, Hechevarría-Pupo Rr, Pérez-González, Luis Velázquez-Pérez
Publikováno v:
Revista de Neurología. 33:10
INTRODUCTION A patient with type 2 spino cerebellar ataxia has difficulty in carrying out alternate movements such as pronation and supination. OBJECTIVES. To evaluate the function of an automatized system for measuring disorders of alternate movemen
Autor:
L. E., Almaguer Mederos, D., Almaguer Gotay, Y., González Zaldívar, E., Martínez Góngora, P., Bahr Valcárcel
Publikováno v:
Revista Mexicana de Neurociencia; may/jun2005, Vol. 6 Issue 3, p201-206, 6p
Autor:
Almaguer Mederos, L. E., Proenza, C. L., Almira, Y. Rodríguez, Batallán, K. Escalona, Falcón, N. Santos, E. Martínez Góngora, Almarales, D. Cuello, L. Velásquez Pérez, Herrera, M. Paneque
Publikováno v:
Clinical Genetics; Dec2008, Vol. 74 Issue 6, p571-573, 3p, 1 Chart, 1 Graph