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H Barros

Showing results (191-200 of 201) with videos related to

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BJOG : an International Journal of Obstetrics and Gynaecology|March 16, 2017
Changes in management policies for extremely preterm births and neonatal outcomes from 2003 to 2012: two population-based studies in ten European regionsM Bonet, M Cuttini, A Piedvache, et al.
Plos One|December 7, 2021
Effects of population mobility on the COVID-19 spread in BrazilEduarda T C Chagas, Pedro H Barros, Isadora Cardoso-Pereira, et al.
HIV Medicine|December 6, 2011
Population mobility and the changing epidemics of HIV-2 in PortugalA C Carvalho, E Valadas, L França, et al.
Journal of Epidemiology and Community Health|August 15, 2009
The European Perinatal Health Report: comparing the health and care of pregnant women and newborn babies in EuropeJennifer Zeitlin, Ashna Mohangoo, Marina Cuttini, et al.
American Journal of Human Genetics|October 2, 2012
Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutationBeatriz Garcia-Diaz, Mario H Barros, Simone Sanna-Cherchi, et al.
ACS Omega|April 28, 2025
Synthesis of BaSiH<sub>6</sub> Hydridosilicate at High Pressures-A Bridge to BaSiH<sub>8</sub> PolyhydrideDoreen C Beyer, Kristina Spektor, Olga Yu Vekilova, et al.
Archives of Biochemistry and Biophysics|April 4, 2019
Mutations of Cys and Ser residues in the α5-subunit of the 20S proteasome from Saccharomyces cerevisiae affects gating and chronological lifespanJanaína M M Leme, Erina Ohara, Verônica F Santiago, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 13, 2018
Metabolic studies of a patient harbouring a novel S487L mutation in the catalytic subunit of AMPKJuliana Harumi Arita, Mário H Barros, Felipe Gustavo Ravagnani, et al.
American Journal of Human Genetics|March 6, 2008
ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiencyClotilde Lagier-Tourenne, Meriem Tazir, Luis Carlos López, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|February 21, 2019
Impact of maternal body mass index and gestational weight gain on pregnancy complications: an individual participant data meta-analysis of European, North American and Australian cohortsS Santos, E Voerman, P Amiano, et al.
Pageof 21

Showing results (191-200 of 201) with videos related to

Sort By:
Pageof 21
BJOG : an International Journal of Obstetrics and Gynaecology|March 16, 2017
Changes in management policies for extremely preterm births and neonatal outcomes from 2003 to 2012: two population-based studies in ten European regionsM Bonet, M Cuttini, A Piedvache, et al.
Plos One|December 7, 2021
Effects of population mobility on the COVID-19 spread in BrazilEduarda T C Chagas, Pedro H Barros, Isadora Cardoso-Pereira, et al.
HIV Medicine|December 6, 2011
Population mobility and the changing epidemics of HIV-2 in PortugalA C Carvalho, E Valadas, L França, et al.
Journal of Epidemiology and Community Health|August 15, 2009
The European Perinatal Health Report: comparing the health and care of pregnant women and newborn babies in EuropeJennifer Zeitlin, Ashna Mohangoo, Marina Cuttini, et al.
American Journal of Human Genetics|October 2, 2012
Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutationBeatriz Garcia-Diaz, Mario H Barros, Simone Sanna-Cherchi, et al.
ACS Omega|April 28, 2025
Synthesis of BaSiH<sub>6</sub> Hydridosilicate at High Pressures-A Bridge to BaSiH<sub>8</sub> PolyhydrideDoreen C Beyer, Kristina Spektor, Olga Yu Vekilova, et al.
Archives of Biochemistry and Biophysics|April 4, 2019
Mutations of Cys and Ser residues in the α5-subunit of the 20S proteasome from Saccharomyces cerevisiae affects gating and chronological lifespanJanaína M M Leme, Erina Ohara, Verônica F Santiago, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 13, 2018
Metabolic studies of a patient harbouring a novel S487L mutation in the catalytic subunit of AMPKJuliana Harumi Arita, Mário H Barros, Felipe Gustavo Ravagnani, et al.
American Journal of Human Genetics|March 6, 2008
ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiencyClotilde Lagier-Tourenne, Meriem Tazir, Luis Carlos López, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|February 21, 2019
Impact of maternal body mass index and gestational weight gain on pregnancy complications: an individual participant data meta-analysis of European, North American and Australian cohortsS Santos, E Voerman, P Amiano, et al.
Pageof 21