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I Lopes

Showing results (211-220 of 240) with videos related to

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American Journal of Human Genetics|October 3, 1998
Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24H A Phillips, I E Scheffer, K M Crossland, et al.
Epilepsy Research|March 27, 1999
Congenital malformations due to antiepileptic drugsS Kaneko, D Battino, E Andermann, et al.
Cellular and Molecular Neurobiology|January 21, 2022
Modulating Expression of Endogenous Interleukin 1 Beta in the Acute Phase of the Pilocarpine Model of Epilepsy May Change Animal SurvivalV D B Pascoal, R B Marchesini, M C P Athié, et al.
Neurology|March 31, 2010
Relationship between environmental factors and gray matter atrophy in refractory MTLEC L Yasuda, M E Morita, A Alessio, et al.
Nature Genetics|October 15, 1998
Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsyB A Minassian, J R Lee, J A Herbrick, et al.
ACS Applied Materials & Interfaces|June 29, 2021
Bacterial Photoinactivation Using PLGA Electrospun ScaffoldsAline O Pereira, Isabella M I Lopes, Thiago R Silva, et al.
Neurology|January 1, 1996
Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patientsI Silveira, I Lopes-Cendes, S Kish, et al.
Arquivos De Neuro-Psiquiatria|June 18, 1998
Frequency of the different mutations causing spinocerebellar ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a large group of Brazilian patientsI Lopes-Cendes, H G Teive, M E Calcagnotto, et al.
Clinical Endocrinology|March 21, 2021
Genetic and clinical aspects of paediatric pheochromocytomas and paragangliomasJanaina Petenuci, Augusto G Guimaraes, Gustavo F C Fagundes, et al.
American Journal of Human Genetics|January 3, 2001
Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype studyC Gaspar, I Lopes-Cendes, S Hayes, et al.
Pageof 24

Showing results (211-220 of 240) with videos related to

Sort By:
Pageof 24
American Journal of Human Genetics|October 3, 1998
Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24H A Phillips, I E Scheffer, K M Crossland, et al.
Epilepsy Research|March 27, 1999
Congenital malformations due to antiepileptic drugsS Kaneko, D Battino, E Andermann, et al.
Cellular and Molecular Neurobiology|January 21, 2022
Modulating Expression of Endogenous Interleukin 1 Beta in the Acute Phase of the Pilocarpine Model of Epilepsy May Change Animal SurvivalV D B Pascoal, R B Marchesini, M C P Athié, et al.
Neurology|March 31, 2010
Relationship between environmental factors and gray matter atrophy in refractory MTLEC L Yasuda, M E Morita, A Alessio, et al.
Nature Genetics|October 15, 1998
Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsyB A Minassian, J R Lee, J A Herbrick, et al.
ACS Applied Materials & Interfaces|June 29, 2021
Bacterial Photoinactivation Using PLGA Electrospun ScaffoldsAline O Pereira, Isabella M I Lopes, Thiago R Silva, et al.
Neurology|January 1, 1996
Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patientsI Silveira, I Lopes-Cendes, S Kish, et al.
Arquivos De Neuro-Psiquiatria|June 18, 1998
Frequency of the different mutations causing spinocerebellar ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a large group of Brazilian patientsI Lopes-Cendes, H G Teive, M E Calcagnotto, et al.
Clinical Endocrinology|March 21, 2021
Genetic and clinical aspects of paediatric pheochromocytomas and paragangliomasJanaina Petenuci, Augusto G Guimaraes, Gustavo F C Fagundes, et al.
American Journal of Human Genetics|January 3, 2001
Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype studyC Gaspar, I Lopes-Cendes, S Hayes, et al.
Pageof 24