Gatto, Emilia Mabel

PRODUCCION CIENTÍFICO TECNOLÓGICA

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Artículo Clinical and genetic characteristics in patients with Huntington's Disease from Argentina

Gatto, Emilia Mabel; Parisi, Virginia; Persi, Gabriel; Converso, Daniela Paola ; Etcheverry, José Luis; Varela, Viviana ; Alba, Liliana; Fretchel, Gustavo (Elsevier, 2012-02)
Artículo Deficits in temporal processing correlate with clinical progression in Huntington's disease

Agostino, Patricia ; Gatto, Emilia Mabel; Cesarini, M.; Etcheverry, J.L.; Sanguinetti, A.; Golombek, Diego Andrés (Wiley Blackwell Publishing, Inc, 2017-02)
Artículo Intrafamilial variable phenotype including corticobasal syndrome in a family with p.P301L mutation in the MAPT gene: first report in South America

Gatto, Emilia Mabel; Allegri, Ricardo Francisco ; Da Prat, Gustavo; Chrem Mendez, Patricio Alexis; Hanna, David S.; Dorschner, Michael O.; Surace, Ezequiel Ignacio ; Zabetian, Cyrus P.; Mata, Ignacio F. (Elsevier Science Inc, 2016-12)
Artículo Overexpression of neutrophil neuronal nitric oxide synthase in Parkinson's disease

Gatto, Emilia Mabel; Riobó, Natalia A.; Carreras, Maria Cecilia ; Cherñavsky, Alejandra Claudia ; Rubio, Andrea; Satz, M. Leonardo; Poderoso, Juan José (Academic Press Inc Elsevier Science, 2000-06)
Artículo Pantothenate kinase-associated neurodegeneration: Novel mutations in the PANK2 gene in an argentinean young woman

Gatto, Emilia Mabel; Etcheverry, Jose L.; Converso, Daniela Paola ; Bidinost, Carla; Rosa, Alberto Luis (Wiley-liss, div John Wiley & Sons Inc., 2010-10-15)
Artículo The LRRK2 G2019S mutation in a series of Argentinean patients with Parkinson's disease: Clinical and demographic characteristics

Gatto, Emilia Mabel; Parisi, Virginia; Converso, Daniela Paola ; Poderoso, Juan José ; Carreras, Maria Cecilia ; Martí Massó, José Félix; Paisán Ruiz, Coro (Elsevier Ireland, 2013-03)

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