Search Results - "Vidal, Lídice"

The new mutation, E46K, of α-synuclein causes parkinson and Lewy body dementia by Zarranz, Juan J., Alegre, Javier, Gómez-Esteban, Juan C., Lezcano, Elena, Ros, Raquel, Ampuero, Israel, Vidal, Lídice, Hoenicka, Janet, Rodriguez, Olga, Atarés, Begoña, Llorens, Verónica, Tortosa, Estrella Gomez, del Ser, Teodoro, Muñoz, David G., de Yebenes, Justo G.

“…Familial parkinsonism and dementia with cortical and subcortical Lewy bodies is uncommon, and no genetic defect has been reported in the previously described…”
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Genetic linkage of autosomal dominant progressive supranuclear palsy to 1q31.1 by Ros, Raquel, Gómez Garre, Pilar, Hirano, Michio, Tai, Yen F., Ampuero, Israel, Vidal, Lídice, Rojo, Ana, Fontan, Aurora, Vazquez, Ana, Fanjul, Samira, Hernandez, Jaime, Cantarero, Susana, Hoenicka, Janet, Jones, Alison, Ahsan, R. Laila, Pavese, Nicola, Piccini, Paola, Brooks, David J., Perez-Tur, Jordi, Nyggard, Torbjorn, de Yébenes, Justo G.

“…Progressive supranuclear palsy (PSP) is a disorder of unknown pathogenesis. Familial clusters of PSP have been reported related to mutations of protein tau. We…”
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Molecular findings in familial Parkinson disease in Spain by Hoenicka, Janet, Vidal, Lídice, Morales, Blas, Ampuero, Israel, Jiménez-Jiménez, F Javier, Berciano, Jose, del Ser, Teodoro, Jiménez, Adriano, Ruíz, Pedro G, de Yébenes, Justo G

“…Several genetic errors in alpha-synuclein (Park1) and ubiquitin carboxyl-terminal-hydrolase L1(Park5) genes cause autosomal dominant familial Parkinson…”
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Familial focal dystonia by Jiménez-Jiménez, Félix Javier, Martínez-Castrillo, Juan Carlos, Barón-Rubio, Manuel, Zurdo, José Martin, de Toledo-Heras, Maria, Vidal, Lídice, Hoenicka, Janette

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Steele-Richardson-Olszewski syndrome in a patient with a single C212Y mutation in the parkin protein by Morales, Blas, Martínez, Armando, Gonzalo, Isabel, Vidal, Lidice, Ros, Raquel, Gomez-Tortosa, Estrella, Rabano, Alberto, Ampuero, Israel, Sánchez, Marina, Hoenicka, Janet, García de Yébenes, Justo

“…Steele‐Richardson‐Olszewski syndrome (SROS) is a neurodegenerative disorder of unknown aetiology, most frequently sporadic. Familial cases of SROS have been…”
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Evaluación conductual del modelo de lesión unilateral en ratas con 6-hidroxidopamina. Correlación entre las rotaciones inducidas por D anfetamina, apomorfina y la prueba de habilidades manuales by Pavón Fuentes, Nancy, Vidal, Lídice, Álvarez Fonseca, Pío, Blanco Lezcano, Lisette, Torres Montoya, Abel, Rodríguez, Aliet, Macías González, Raúl

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Trasplante simultáneo de células mesencefálicas fetales en striatum y globus pallidus de ratas con lesión por 6-hidroxidopamina by Álvarez Fonseca, Pío, Blanco Lezcano, Lisette, Pavón Fuentes, Nancy, Vidal, Lídice, Castellano Benítez, Orlando, Castillo Díaz, Lázara, García Cruz, Andrés, Rosillo Martí, Juan Carlos, Macías González, Raúl

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Factores que desencadenan la muerte neuronal en enfermedades neurodegenerativas by Pavón Fuentes, Nancy, Vidal, Lídice, Blanco Lezcano, Lisette, Álvarez Fonseca, Pío, Torres Montoya, Abel, Lorigados Pedre, Lourdes, Álvarez González, Lázaro, Macías González, Raúl

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