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E Herman

Showing results (481-490 of 696) with videos related to

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American Journal of Orthopedics (Belle Mead, N.J.)|December 5, 2002
Issues in surgical treatment of thoraco-lumbar injuries associated with spinal cord injuries in children and adolescentsHaluk Altiok, Anis Mekhail, Lawrence C Vogel, et al.
American Journal of Medical Genetics. Part A|September 11, 2003
Left-sided CHILD syndrome caused by a nonsense mutation in the NSDHL geneMarybeth Hummel, David Cunningham, Charles J Mullett, et al.
Biochemical and Biophysical Research Communications|April 25, 2006
Pbx1 and Meis1 regulate activity of the Xenopus laevis Zic3 promoter through a highly conserved regionLisa E Kelly, Tessa L Carrel, Gail E Herman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 7, 2009
The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephalyElizabeth A Varga, Matthew Pastore, Thomas Prior, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|May 1, 1996
Gastric antral vascular ectasia: a case report and review of the literatureB E Herman, J J Vargo, S Baum, et al.
The Journal of Surgical Research|December 6, 2025
Implemented Interventions for Surgeon Well-Being: A Scoping ReviewRodney Ahdoot, Alexandra E Herman, Bhuvan Pottepalem, et al.
JAMA|March 15, 2003
Newborns killed or left to die by a parent: a population-based studyMarcia E Herman-Giddens, Jamie B Smith, Manjoo Mittal, et al.
The Journal of Craniofacial Surgery|April 1, 1993
Effects of skeletal fixation on craniofacial imagingB L Eppley, C Sparks, E Herman, et al.
Human Mutation|January 17, 2002
Characterization of mutations in fifty North American patients with X-linked myotubular myopathyGail E Herman, Kevin Kopacz, Wei Zhao, et al.
Human Molecular Genetics|November 3, 2009
Significant contributions of the extraembryonic membranes and maternal genotype to the placental pathology in heterozygous Nsdhl deficient female embryosDavid Cunningham, Tiffany Talabere, Natalie Bir, et al.
Pageof 70

Showing results (481-490 of 696) with videos related to

Sort By:
Pageof 70
American Journal of Orthopedics (Belle Mead, N.J.)|December 5, 2002
Issues in surgical treatment of thoraco-lumbar injuries associated with spinal cord injuries in children and adolescentsHaluk Altiok, Anis Mekhail, Lawrence C Vogel, et al.
American Journal of Medical Genetics. Part A|September 11, 2003
Left-sided CHILD syndrome caused by a nonsense mutation in the NSDHL geneMarybeth Hummel, David Cunningham, Charles J Mullett, et al.
Biochemical and Biophysical Research Communications|April 25, 2006
Pbx1 and Meis1 regulate activity of the Xenopus laevis Zic3 promoter through a highly conserved regionLisa E Kelly, Tessa L Carrel, Gail E Herman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 7, 2009
The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephalyElizabeth A Varga, Matthew Pastore, Thomas Prior, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|May 1, 1996
Gastric antral vascular ectasia: a case report and review of the literatureB E Herman, J J Vargo, S Baum, et al.
The Journal of Surgical Research|December 6, 2025
Implemented Interventions for Surgeon Well-Being: A Scoping ReviewRodney Ahdoot, Alexandra E Herman, Bhuvan Pottepalem, et al.
JAMA|March 15, 2003
Newborns killed or left to die by a parent: a population-based studyMarcia E Herman-Giddens, Jamie B Smith, Manjoo Mittal, et al.
The Journal of Craniofacial Surgery|April 1, 1993
Effects of skeletal fixation on craniofacial imagingB L Eppley, C Sparks, E Herman, et al.
Human Mutation|January 17, 2002
Characterization of mutations in fifty North American patients with X-linked myotubular myopathyGail E Herman, Kevin Kopacz, Wei Zhao, et al.
Human Molecular Genetics|November 3, 2009
Significant contributions of the extraembryonic membranes and maternal genotype to the placental pathology in heterozygous Nsdhl deficient female embryosDavid Cunningham, Tiffany Talabere, Natalie Bir, et al.
Pageof 70