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H Mandel

Showing results (121-130 of 188) with videos related to

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Annals of Work Exposures and Health|October 24, 2018
Ambient Fine Aerosol Concentrations in Multiple Metrics in Taconite Mining OperationsTran Huynh, Gurumurthy Ramachandran, Harrison Quick, et al.
Professional Psychology, Research and Practice|January 26, 2016
Serving Transgender Youth: Challenges, Dilemmas and Clinical ExamplesAmy C Tishelman, Randi Kaufman, Laura Edwards-Leeper, et al.
Clinical Genetics|December 15, 2015
Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenitaN Ekhilevitch, A Kurolap, D Oz-Levi, et al.
Journal of Occupational and Environmental Medicine|July 24, 1998
An epidemiologic investigation of reproductive hormones in men with occupational exposure to perfluorooctanoic acidG W Olsen, F D Gilliland, M M Burlew, et al.
American Journal of Perinatology|April 1, 1997
Corticosteroid binding globulin, total serum cortisol, and stress in extremely low-birth-weight infantsC E Hanna, P L Jett, M R Laird, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Further studies on erythrocyte thiamin transport and phosphorylation in seven patients with thiamin-responsive megaloblastic anaemiaG Rindi, C Patrini, U Laforenza, et al.
Annals of Work Exposures and Health|December 5, 2021
Reconstructing Historical Exposures to Respirable Dust and Respirable Silica in the Taconite Mining Industry for 1955-2010Yuan Shao, Jooyeon Hwang, Richard F MacLehose, et al.
Archives of Internal Medicine|April 1, 1988
Preparation for practice in internal medicine. A study of ten years of residency graduatesJ H Mandel, E C Rich, M G Luxenberg, et al.
Human Molecular Genetics|May 1, 1997
Profound biotinidase deficiency caused by a point mutation that creates a downstream cryptic 3' splice acceptor site within an exon of the human biotinidase geneR J Pomponio, T R Reynolds, H Mandel, et al.
Human Genetics|December 18, 1998
Refined mapping of the gene for thiamine-responsive megaloblastic anemia syndrome and evidence for genetic homogeneityT Raz, T Barrett, R Szargel, et al.
Pageof 19

Showing results (121-130 of 188) with videos related to

Sort By:
Pageof 19
Annals of Work Exposures and Health|October 24, 2018
Ambient Fine Aerosol Concentrations in Multiple Metrics in Taconite Mining OperationsTran Huynh, Gurumurthy Ramachandran, Harrison Quick, et al.
Professional Psychology, Research and Practice|January 26, 2016
Serving Transgender Youth: Challenges, Dilemmas and Clinical ExamplesAmy C Tishelman, Randi Kaufman, Laura Edwards-Leeper, et al.
Clinical Genetics|December 15, 2015
Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenitaN Ekhilevitch, A Kurolap, D Oz-Levi, et al.
Journal of Occupational and Environmental Medicine|July 24, 1998
An epidemiologic investigation of reproductive hormones in men with occupational exposure to perfluorooctanoic acidG W Olsen, F D Gilliland, M M Burlew, et al.
American Journal of Perinatology|April 1, 1997
Corticosteroid binding globulin, total serum cortisol, and stress in extremely low-birth-weight infantsC E Hanna, P L Jett, M R Laird, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Further studies on erythrocyte thiamin transport and phosphorylation in seven patients with thiamin-responsive megaloblastic anaemiaG Rindi, C Patrini, U Laforenza, et al.
Annals of Work Exposures and Health|December 5, 2021
Reconstructing Historical Exposures to Respirable Dust and Respirable Silica in the Taconite Mining Industry for 1955-2010Yuan Shao, Jooyeon Hwang, Richard F MacLehose, et al.
Archives of Internal Medicine|April 1, 1988
Preparation for practice in internal medicine. A study of ten years of residency graduatesJ H Mandel, E C Rich, M G Luxenberg, et al.
Human Molecular Genetics|May 1, 1997
Profound biotinidase deficiency caused by a point mutation that creates a downstream cryptic 3' splice acceptor site within an exon of the human biotinidase geneR J Pomponio, T R Reynolds, H Mandel, et al.
Human Genetics|December 18, 1998
Refined mapping of the gene for thiamine-responsive megaloblastic anemia syndrome and evidence for genetic homogeneityT Raz, T Barrett, R Szargel, et al.
Pageof 19