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Saul Lindo Samanamud
Saul Lindo Samanamud
School of Human Medicine - UNICAMP
Verified email at dac.unicamp.br
Title
Cited by
Cited by
Year
Clinical and molecular features of late onset Huntington disease in a Peruvian cohort
MR Cornejo-Olivas, MA Inca-Martinez, K Espinoza-Huertas, D Veliz-Otani, ...
Journal of Huntington's disease 4 (1), 99-105, 2015
332015
Clinical and molecular studies reveal a PSEN1 mutation (L153V) in a Peruvian family with early-onset Alzheimer's disease
MR Cornejo-Olivas, CE Yu, P Mazzetti, IF Mata, M Meza, ...
Neuroscience letters 563, 140-143, 2014
152014
Spinocerebellar Ataxia Type 10 or SCA10 in Peruvian Population. First Report of Three Families (PD2. 006)
MC Olivas, I Cornejo-Herrera, S Lindo-Samanamud, R Castilhos, ...
Neurology 80 (7 Supplement), PD2. 006-PD2. 006, 2013
42013
Enfermedad de Kennedy en el Perú: Primeros casos con diagnóstico molecular
V Gómez-Calero, M Cornejo-Olivas, O Ortega, V Marca, ...
Revista Peruana de Medicina Experimental y Salud Pública 30, 331-335, 2013
22013
Estrategia de genotipado del gen FMR1: Método de diagnóstico alternativo para el Síndrome X Frágil y otras enfermedades por expansión de trinucleotidos
S Lindo-Samanamud, M Cornejo-Olivas, O Ortega, V Marca, ...
Revista Medica Herediana 24 (4), 269-276, 2013
12013
Asociación entre el polimorfismo genético de la apolipoproteína E (ApoE) y la enfermedad de Parkinson
V Marca, O Acosta, L Torres, O Ortega, M Cornejo-Olivas, ...
Anales de la Facultad de Medicina 74 (3), 169-174, 2013
12013
Kennedy disease in Peru: first cases with molecular diagnosis
V Gómez-Calero, M Cornejo-Olivas, O Ortega, V Marca, ...
Revista Peruana de Medicina Experimental y Salud Publica 30 (2), 331-335, 2013
12013
Clinical and Molecular Studies Reveal a PSEN1 Mutation (L153V) in a Peruvian Family with Early-Onset Alzheimer's Disease (P05. 072)
MC Olivas, J Leverenz, S Lindo-Samanamud, I Mata, PM Soler, ...
Neurology 78 (1 Supplement), P05. 072-P05. 072, 2012
12012
Clinical and Molecular Features of Myotonic Dystrophy Type 1 in Peru (P5. 066)
K Milla-Neyra, M Inca-Martinez, O Ortega-Davila, V Marca, ...
Neurology 86 (16_supplement), P5. 066, 2016
2016
Clinical and Molecular Features of Late Onset Huntington Disease in a Peruvian Cohort
MR Velit-Salazar, IF Cornejo-Herrera, MA Inca-Martinez, P Mora-Alferez, ...
IOS Press, 2015
2015
Allelic distribution of the normal ATXN3 gene in a Peruvian mestizo population
MR Cornejo-Olivas, KA Espinoza-Huertas, S Lindo-Samanamud, ...
MOVEMENT DISORDERS 29, S470-S470, 2014
2014
Association between apolipoprotein E (ApoE) genetic polymorphism and Parkinson's disease.
V Marca, O Acosta, L Torres, O Ortega, M Cornejo-Olivas, ...
2013
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