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Wambach

Showing results (241-250 of 285) with videos related to

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JAMA Psychiatry|February 2, 2017
Effect of Disorder-Specific vs Nonspecific Psychotherapy for Chronic Depression: A Randomized Clinical TrialElisabeth Schramm, Levente Kriston, Ingo Zobel, et al.
Journal of the International Neuropsychological Society : JINS|October 22, 2011
Dysexecutive functioning in mild cognitive impairment: derailment in temporal gradientsJoel Eppig, Denene Wambach, Christine Nieves, et al.
Journal of the International Neuropsychological Society : JINS|September 2, 2011
Verbal serial list learning in mild cognitive impairment: a profile analysis of interference, forgetting, and errorsDavid J Libon, Mark W Bondi, Catherine C Price, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 9, 2023
Provision and availability of genomic medicine services in Level IV neonatal intensive care unitsMonica H Wojcik, Katharine P Callahan, Austin Antoniou, et al.
American Journal of Respiratory Cell and Molecular Biology|May 6, 2026
Lentiviral-mediated gene complementation to rescue pathogenic ABCA3 variantsAshley L Cooney, Shakayla Lamer, Ping Yang, et al.
Pediatric Research|March 5, 2008
Population and disease-based prevalence of the common mutations associated with surfactant deficiencyTami H Garmany, Jennifer A Wambach, Hillary B Heins, et al.
Biorxiv : the Preprint Server for Biology|September 5, 2025
Lentiviral-mediated gene complementation rescues pathogenic <i>ABCA3</i> variantsAshley L Cooney, Shakayla Lamer, Ping Yang, et al.
Pediatric Research|July 4, 2018
Functional characterization of biallelic RTTN variants identified in an infant with microcephaly, simplified gyral pattern, pontocerebellar hypoplasia, and seizuresJennifer A Wambach, Daniel J Wegner, Ping Yang, et al.
American Journal of Medical Genetics. Part A|May 1, 2021
Biallelic ASCC1 variants including a novel intronic variant result in expanded phenotypic spectrum of spinal muscular atrophy with congenital bone fractures 2 (SMABF2)Kristen K Rosano, Daniel J Wegner, Marwan Shinawi, et al.
Clinical Epigenetics|April 10, 2019
Novel parent-of-origin-specific differentially methylated loci on chromosome 16Katharina V Schulze, Przemyslaw Szafranski, Harry Lesmana, et al.
Pageof 29

Showing results (241-250 of 285) with videos related to

Sort By:
Pageof 29
JAMA Psychiatry|February 2, 2017
Effect of Disorder-Specific vs Nonspecific Psychotherapy for Chronic Depression: A Randomized Clinical TrialElisabeth Schramm, Levente Kriston, Ingo Zobel, et al.
Journal of the International Neuropsychological Society : JINS|October 22, 2011
Dysexecutive functioning in mild cognitive impairment: derailment in temporal gradientsJoel Eppig, Denene Wambach, Christine Nieves, et al.
Journal of the International Neuropsychological Society : JINS|September 2, 2011
Verbal serial list learning in mild cognitive impairment: a profile analysis of interference, forgetting, and errorsDavid J Libon, Mark W Bondi, Catherine C Price, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 9, 2023
Provision and availability of genomic medicine services in Level IV neonatal intensive care unitsMonica H Wojcik, Katharine P Callahan, Austin Antoniou, et al.
American Journal of Respiratory Cell and Molecular Biology|May 6, 2026
Lentiviral-mediated gene complementation to rescue pathogenic ABCA3 variantsAshley L Cooney, Shakayla Lamer, Ping Yang, et al.
Pediatric Research|March 5, 2008
Population and disease-based prevalence of the common mutations associated with surfactant deficiencyTami H Garmany, Jennifer A Wambach, Hillary B Heins, et al.
Biorxiv : the Preprint Server for Biology|September 5, 2025
Lentiviral-mediated gene complementation rescues pathogenic <i>ABCA3</i> variantsAshley L Cooney, Shakayla Lamer, Ping Yang, et al.
Pediatric Research|July 4, 2018
Functional characterization of biallelic RTTN variants identified in an infant with microcephaly, simplified gyral pattern, pontocerebellar hypoplasia, and seizuresJennifer A Wambach, Daniel J Wegner, Ping Yang, et al.
American Journal of Medical Genetics. Part A|May 1, 2021
Biallelic ASCC1 variants including a novel intronic variant result in expanded phenotypic spectrum of spinal muscular atrophy with congenital bone fractures 2 (SMABF2)Kristen K Rosano, Daniel J Wegner, Marwan Shinawi, et al.
Clinical Epigenetics|April 10, 2019
Novel parent-of-origin-specific differentially methylated loci on chromosome 16Katharina V Schulze, Przemyslaw Szafranski, Harry Lesmana, et al.
Pageof 29