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Neuroimage
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August 10, 2014
Simplified gyral pattern in severe developmental microcephalies? New insights from allometric modeling for spatial and spectral analysis of gyrification
D Germanaud, J Lefèvre, C Fischer, et al.
Memorias Do Instituto Oswaldo Cruz
|
September 18, 2008
Prevalence and clinical aspects of respiratory syncytial virus A and B groups in children seen at Hospital de Clínicas of Uberlândia, MG, Brazil
T F M Oliveira, G R O Freitas, L Z G Ribeiro, et al.
European Journal of Human Genetics : EJHG
|
October 22, 2015
West syndrome caused by homozygous variant in the evolutionary conserved gene encoding the mitochondrial elongation factor GUF1
Ali Abdullah Alfaiz, Verena Müller, Nadia Boutry-Kryza, et al.
American Journal of Medical Genetics
|
August 18, 2000
Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation
T Bienvenu, V des Portes, N McDonell, et al.
The Brazilian Journal of Infectious Diseases : an Official Publication of the Brazilian Society of Infectious Diseases
|
February 22, 2015
High degree of concordance between flow cytometry and geno2pheno methods for HIV-1 tropism determination in proviral DNA
Alex José Leite Torres, Luis Fernando de Macedo Brígido, Marcos Herculano Nunes Abrahão, et al.
American Journal of Human Genetics
|
May 27, 2004
Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardation
Kristine Freude, Kirsten Hoffmann, Lars-Riff Jensen, et al.
Neurogenetics
|
August 8, 2008
The location of DCX mutations predicts malformation severity in X-linked lissencephaly
Pierre-Louis Leger, Isabelle Souville, Nathalie Boddaert, et al.
Journal of Neuroscience Research
|
June 3, 2017
Overexpression of α-synuclein in an astrocyte cell line promotes autophagy inhibition and apoptosis
Adolfo Garcia Erustes, Fernanda Yakel Stefani, Juliana Yoshie Terashima, et al.
BMC Nursing
|
July 2, 2025
Social representations of COVID-19 by the nursing team of an intensive care unit
Rafael Celestino da Silva, Bruna Gonçalves Ribeiro Araujo, Letícia Braga Portes Alves Rentz, et al.
Brazilian Journal of Otorhinolaryngology
|
August 3, 2025
Adenoid hypertrophy is directly associated with the severity of OSA in obese children: A pilot study
Victor Hugo da Costa Ferreira, Carolina Sponchiado Miura, Bruna de Alencar Custodio Lupoli, et al.
Page
of 67
Search research articles
Search
Showing results (541-550 of 669) with videos related to
Sort By:
Page
of 67
Neuroimage
|
August 10, 2014
Simplified gyral pattern in severe developmental microcephalies? New insights from allometric modeling for spatial and spectral analysis of gyrification
D Germanaud, J Lefèvre, C Fischer, et al.
Memorias Do Instituto Oswaldo Cruz
|
September 18, 2008
Prevalence and clinical aspects of respiratory syncytial virus A and B groups in children seen at Hospital de Clínicas of Uberlândia, MG, Brazil
T F M Oliveira, G R O Freitas, L Z G Ribeiro, et al.
European Journal of Human Genetics : EJHG
|
October 22, 2015
West syndrome caused by homozygous variant in the evolutionary conserved gene encoding the mitochondrial elongation factor GUF1
Ali Abdullah Alfaiz, Verena Müller, Nadia Boutry-Kryza, et al.
American Journal of Medical Genetics
|
August 18, 2000
Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation
T Bienvenu, V des Portes, N McDonell, et al.
The Brazilian Journal of Infectious Diseases : an Official Publication of the Brazilian Society of Infectious Diseases
|
February 22, 2015
High degree of concordance between flow cytometry and geno2pheno methods for HIV-1 tropism determination in proviral DNA
Alex José Leite Torres, Luis Fernando de Macedo Brígido, Marcos Herculano Nunes Abrahão, et al.
American Journal of Human Genetics
|
May 27, 2004
Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardation
Kristine Freude, Kirsten Hoffmann, Lars-Riff Jensen, et al.
Neurogenetics
|
August 8, 2008
The location of DCX mutations predicts malformation severity in X-linked lissencephaly
Pierre-Louis Leger, Isabelle Souville, Nathalie Boddaert, et al.
Journal of Neuroscience Research
|
June 3, 2017
Overexpression of α-synuclein in an astrocyte cell line promotes autophagy inhibition and apoptosis
Adolfo Garcia Erustes, Fernanda Yakel Stefani, Juliana Yoshie Terashima, et al.
BMC Nursing
|
July 2, 2025
Social representations of COVID-19 by the nursing team of an intensive care unit
Rafael Celestino da Silva, Bruna Gonçalves Ribeiro Araujo, Letícia Braga Portes Alves Rentz, et al.
Brazilian Journal of Otorhinolaryngology
|
August 3, 2025
Adenoid hypertrophy is directly associated with the severity of OSA in obese children: A pilot study
Victor Hugo da Costa Ferreira, Carolina Sponchiado Miura, Bruna de Alencar Custodio Lupoli, et al.
Page
of 67