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G Horovitz

Showing results (81-90 of 95) with videos related to

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Neuroimage|October 1, 2015
Meta-analysis of real-time fMRI neurofeedback studies using individual participant data: How is brain regulation mediated?Kirsten Emmert, Rotem Kopel, James Sulzer, et al.
Elife|August 28, 2015
NUDT21-spanning CNVs lead to neuropsychiatric disease and altered MeCP2 abundance via alternative polyadenylationVincenzo A Gennarino, Callison E Alcott, Chun-An Chen, et al.
International Journal of Molecular Sciences|August 12, 2023
Genotypic-Phenotypic Correlations of Hereditary Hyperferritinemia-Cataract Syndrome: Case Series of Three Brazilian FamiliesOlivia A Zin, Luiza M Neves, Daniela P Cunha, et al.
Genes|January 25, 2025
Genotype-Phenotype Correlations of Nance-Horan Syndrome in Male and Female Carriers of a Novel VariantOlivia A Zin, Luiza M Neves, Fabiana L Motta, et al.
MMWR. Morbidity and Mortality Weekly Report|January 29, 2016
Possible Association Between Zika Virus Infection and Microcephaly - Brazil, 2015Lavinia Schuler-Faccini, Erlane M Ribeiro, Ian M L Feitosa, et al.
Journal of Community Genetics|May 10, 2024
The cost of genetic diagnosis of suspected hereditary pediatric cataracts with whole-exome sequencing from a middle-income country perspective: a mixed costing analysisLuiza M Neves, Márcia Pinto, Olivia A Zin, et al.
Journal of Inherited Metabolic Disease|October 13, 2009
Clinical and biochemical studies in mucopolysaccharidosis type II carriersI V D Schwartz, L L C Pinto, G Breda, et al.
Molecular Genetics and Metabolism|March 8, 2021
Long-term impact of early initiation of enzyme replacement therapy in 34 MPS VI patients: A resurvey studyDafne D G Horovitz, Emília K E A Leão, Erlane M Ribeiro, et al.
Journal of Inherited Metabolic Disease|June 12, 2016
ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomaliesEva Morava, Vera Tiemes, Christian Thiel, et al.
Molecular Genetics and Metabolism|March 29, 2013
Enzyme replacement therapy with galsulfase in 34 children younger than five years of age with MPS VIDafne D G Horovitz, Tatiana S P C Magalhães, Angelina Acosta, et al.
Pageof 10

Showing results (81-90 of 95) with videos related to

Sort By:
Pageof 10
Neuroimage|October 1, 2015
Meta-analysis of real-time fMRI neurofeedback studies using individual participant data: How is brain regulation mediated?Kirsten Emmert, Rotem Kopel, James Sulzer, et al.
Elife|August 28, 2015
NUDT21-spanning CNVs lead to neuropsychiatric disease and altered MeCP2 abundance via alternative polyadenylationVincenzo A Gennarino, Callison E Alcott, Chun-An Chen, et al.
International Journal of Molecular Sciences|August 12, 2023
Genotypic-Phenotypic Correlations of Hereditary Hyperferritinemia-Cataract Syndrome: Case Series of Three Brazilian FamiliesOlivia A Zin, Luiza M Neves, Daniela P Cunha, et al.
Genes|January 25, 2025
Genotype-Phenotype Correlations of Nance-Horan Syndrome in Male and Female Carriers of a Novel VariantOlivia A Zin, Luiza M Neves, Fabiana L Motta, et al.
MMWR. Morbidity and Mortality Weekly Report|January 29, 2016
Possible Association Between Zika Virus Infection and Microcephaly - Brazil, 2015Lavinia Schuler-Faccini, Erlane M Ribeiro, Ian M L Feitosa, et al.
Journal of Community Genetics|May 10, 2024
The cost of genetic diagnosis of suspected hereditary pediatric cataracts with whole-exome sequencing from a middle-income country perspective: a mixed costing analysisLuiza M Neves, Márcia Pinto, Olivia A Zin, et al.
Journal of Inherited Metabolic Disease|October 13, 2009
Clinical and biochemical studies in mucopolysaccharidosis type II carriersI V D Schwartz, L L C Pinto, G Breda, et al.
Molecular Genetics and Metabolism|March 8, 2021
Long-term impact of early initiation of enzyme replacement therapy in 34 MPS VI patients: A resurvey studyDafne D G Horovitz, Emília K E A Leão, Erlane M Ribeiro, et al.
Journal of Inherited Metabolic Disease|June 12, 2016
ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomaliesEva Morava, Vera Tiemes, Christian Thiel, et al.
Molecular Genetics and Metabolism|March 29, 2013
Enzyme replacement therapy with galsulfase in 34 children younger than five years of age with MPS VIDafne D G Horovitz, Tatiana S P C Magalhães, Angelina Acosta, et al.
Pageof 10