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I Lopes

Showing results (171-180 of 240) with videos related to

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European Journal of Human Genetics : EJHG|April 10, 1999
Study of three intragenic polymorphisms in the Machado-Joseph disease gene (MJD1) in relation to genetic instability of the (CAG)n tractP Maciel, C Gaspar, L Guimarães, et al.
Journal of Hazardous Materials|August 30, 2011
Screening evaluation of the ecotoxicity and genotoxicity of soils contaminated with organic and inorganic nanoparticles: the role of ageingR Pereira, T A P Rocha-Santos, F E Antunes, et al.
Acta Endocrinologica (Bucharest, Romania : 2005)|March 9, 2026
LIPOHYPERTHROPHY: NEW TECHNOLOGY, OLD PROBLEMSJ V Rocha, M Vaz Lopes, M de Griné Severino, et al.
Epilepsy Research|November 1, 1995
Genetic linkage studies in familial frontal epilepsy: exclusion of the human chromosome regions homologous to the El-1 mouse locusI Lopes-Cendes, H A Phillips, I E Scheffer, et al.
Brain : a Journal of Neurology|February 1, 1995
Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorderI E Scheffer, K P Bhatia, I Lopes-Cendes, et al.
Journal of Pediatric Urology|January 5, 2019
The evaluation of vesicoureteral reflux among children using contrast-enhanced ultrasound: a literature reviewM E Chua, J K Kim, J S Mendoza, et al.
Microbial Ecology|March 24, 2021
Effects of stress exposure in captivity on physiology and infection in avian hosts: no evidence of increased Borrelia burgdorferi s.l. infectivity to vector ticksA C Norte, P M Araújo, L Augusto, et al.
Environmental Science and Pollution Research International|May 6, 2015
Assessing the ecotoxicity of metal nano-oxides with potential for wastewater treatmentV Nogueira, I Lopes, T A P Rocha-Santos, et al.
Lancet (London, England)|February 26, 1994
Autosomal dominant frontal epilepsy misdiagnosed as sleep disorderI E Scheffer, K P Bhatia, I Lopes-Cendes, et al.
European Journal of Neurology|January 26, 2016
Non-motor symptoms in patients with hereditary spastic paraplegia caused by SPG4 mutationsK R Servelhere, I Faber, J A M Saute, et al.
Pageof 24

Showing results (171-180 of 240) with videos related to

Sort By:
Pageof 24
European Journal of Human Genetics : EJHG|April 10, 1999
Study of three intragenic polymorphisms in the Machado-Joseph disease gene (MJD1) in relation to genetic instability of the (CAG)n tractP Maciel, C Gaspar, L Guimarães, et al.
Journal of Hazardous Materials|August 30, 2011
Screening evaluation of the ecotoxicity and genotoxicity of soils contaminated with organic and inorganic nanoparticles: the role of ageingR Pereira, T A P Rocha-Santos, F E Antunes, et al.
Acta Endocrinologica (Bucharest, Romania : 2005)|March 9, 2026
LIPOHYPERTHROPHY: NEW TECHNOLOGY, OLD PROBLEMSJ V Rocha, M Vaz Lopes, M de Griné Severino, et al.
Epilepsy Research|November 1, 1995
Genetic linkage studies in familial frontal epilepsy: exclusion of the human chromosome regions homologous to the El-1 mouse locusI Lopes-Cendes, H A Phillips, I E Scheffer, et al.
Brain : a Journal of Neurology|February 1, 1995
Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorderI E Scheffer, K P Bhatia, I Lopes-Cendes, et al.
Journal of Pediatric Urology|January 5, 2019
The evaluation of vesicoureteral reflux among children using contrast-enhanced ultrasound: a literature reviewM E Chua, J K Kim, J S Mendoza, et al.
Microbial Ecology|March 24, 2021
Effects of stress exposure in captivity on physiology and infection in avian hosts: no evidence of increased Borrelia burgdorferi s.l. infectivity to vector ticksA C Norte, P M Araújo, L Augusto, et al.
Environmental Science and Pollution Research International|May 6, 2015
Assessing the ecotoxicity of metal nano-oxides with potential for wastewater treatmentV Nogueira, I Lopes, T A P Rocha-Santos, et al.
Lancet (London, England)|February 26, 1994
Autosomal dominant frontal epilepsy misdiagnosed as sleep disorderI E Scheffer, K P Bhatia, I Lopes-Cendes, et al.
European Journal of Neurology|January 26, 2016
Non-motor symptoms in patients with hereditary spastic paraplegia caused by SPG4 mutationsK R Servelhere, I Faber, J A M Saute, et al.
Pageof 24