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Archives of Neurology
|
November 19, 2003
Magnetic resonance imaging abnormalities in familial temporal lobe epilepsy with auditory auras
Eliane Kobayashi, Neide F Santos, Fabio R Torres, et al.
Epilepsy Research
|
August 18, 2006
THE SCN2A gene is not a likely candidate for familial mesial temporal lobe epilepsy
Cláudia Vianna Maurer-Morelli, Rodrigo Secolin, Rafael Breglio Marchesini, et al.
Arquivos De Neuro-Psiquiatria
|
April 11, 2007
Linkage study of voltage-gated potassium channels in familial mesial temporal lobe epilepsy
Cláudia Vianna Maurer-Morelli, Rafael Breglio Marchesini, Rodrigo Secolin, et al.
Oncology Letters
|
June 17, 2014
SLC23A2-05 (rs4987219) and KRAS-LCS6 (rs61764370) polymorphisms in patients with squamous cell carcinoma of the head and neck
Marília Bueno Santiago, Fernando Augusto DE Lima Marson, Rodrigo Secolin, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
July 26, 2021
Slowly progressive behavioral frontotemporal dementia syndrome in a family co-segregating the C9orf72 expansion and a Synaptophysin mutation
Joana Prota, Liara Rizzi, Luciana Bonadia, et al.
Archives of Oral Biology
|
March 20, 2012
Genetic association study between Interleukin 10 gene and dental implant loss
Suzane C Pigossi, Fabiano Alvim-Pereira, Cláudia C Montes, et al.
Genomics
|
April 2, 2008
LINKGEN: a new algorithm to process data in genetic linkage studies
Rodrigo Secolin, Cristiane S Rocha, Fábio R Torres, et al.
Psychiatric Genetics
|
April 24, 2010
Family-based association study for bipolar affective disorder
Rodrigo Secolin, Cláudio E M Banzato, Maria C M Oliveira, et al.
Plos One
|
July 2, 2015
Neurocysticercotic Calcifications and Hippocampal Sclerosis: A Case-Control Study
Mateus de Oliveira Taveira, Marcia Elisabete Morita, Clarissa Lin Yasuda, et al.
Genetics and Molecular Biology
|
June 4, 2011
Interactions of polymorphisms in different clock genes associated with circadian phenotypes in humans
Mario Pedrazzoli, Rodrigo Secolin, Luiz Otávio Bastos Esteves, et al.
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of 5
Search research articles
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Showing results (11-20 of 48) with videos related to
Sort By:
Page
of 5
Archives of Neurology
|
November 19, 2003
Magnetic resonance imaging abnormalities in familial temporal lobe epilepsy with auditory auras
Eliane Kobayashi, Neide F Santos, Fabio R Torres, et al.
Epilepsy Research
|
August 18, 2006
THE SCN2A gene is not a likely candidate for familial mesial temporal lobe epilepsy
Cláudia Vianna Maurer-Morelli, Rodrigo Secolin, Rafael Breglio Marchesini, et al.
Arquivos De Neuro-Psiquiatria
|
April 11, 2007
Linkage study of voltage-gated potassium channels in familial mesial temporal lobe epilepsy
Cláudia Vianna Maurer-Morelli, Rafael Breglio Marchesini, Rodrigo Secolin, et al.
Oncology Letters
|
June 17, 2014
SLC23A2-05 (rs4987219) and KRAS-LCS6 (rs61764370) polymorphisms in patients with squamous cell carcinoma of the head and neck
Marília Bueno Santiago, Fernando Augusto DE Lima Marson, Rodrigo Secolin, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
July 26, 2021
Slowly progressive behavioral frontotemporal dementia syndrome in a family co-segregating the C9orf72 expansion and a Synaptophysin mutation
Joana Prota, Liara Rizzi, Luciana Bonadia, et al.
Archives of Oral Biology
|
March 20, 2012
Genetic association study between Interleukin 10 gene and dental implant loss
Suzane C Pigossi, Fabiano Alvim-Pereira, Cláudia C Montes, et al.
Genomics
|
April 2, 2008
LINKGEN: a new algorithm to process data in genetic linkage studies
Rodrigo Secolin, Cristiane S Rocha, Fábio R Torres, et al.
Psychiatric Genetics
|
April 24, 2010
Family-based association study for bipolar affective disorder
Rodrigo Secolin, Cláudio E M Banzato, Maria C M Oliveira, et al.
Plos One
|
July 2, 2015
Neurocysticercotic Calcifications and Hippocampal Sclerosis: A Case-Control Study
Mateus de Oliveira Taveira, Marcia Elisabete Morita, Clarissa Lin Yasuda, et al.
Genetics and Molecular Biology
|
June 4, 2011
Interactions of polymorphisms in different clock genes associated with circadian phenotypes in humans
Mario Pedrazzoli, Rodrigo Secolin, Luiz Otávio Bastos Esteves, et al.
Page
of 5