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Leppert

Showing results (931-940 of 1,307) with videos related to

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Circulation|October 16, 2025
Opportunistic Detection of Coronary Artery Calcium on Noncardiac Chest Computed Tomography: An Emerging Tool for Cardiovascular Disease Prevention: A Scientific Statement From the American Heart AssociationRandi Foraker, Laurence Sperling, Lisa Bratzke, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 3, 2021
Osteoporosis, Fractures, and Bone Mineral Density Screening in Veterans With Kidney Stone DiseaseCalyani Ganesan, I-Chun Thomas, Ruth Romero, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|July 18, 2022
Minocycline treatment in clinically isolated syndrome and serum NfL, GFAP, and metalloproteinase levelsCarlos Camara-Lemarroy, Luanne Metz, Jens Kuhle, et al.
Cancer Research|November 11, 1998
The inducible prostaglandin biosynthetic enzyme, cyclooxygenase 2, is not mutated in patients with attenuated adenomatous polyposis coliL N Spirio, D A Dixon, J Robertson, et al.
Developmental Medicine and Child Neurology|June 4, 1999
Sequential neuromotor examination in children with intrauterine cocaine/polydrug exposureH M Belcher, B K Shapiro, M Leppert, et al.
Nature Communications|February 12, 2020
Serum neurofilament light levels in normal aging and their association with morphologic brain changesMichael Khalil, Lukas Pirpamer, Edith Hofer, et al.
Frontiers in Stroke|July 25, 2025
Identification of Specific Recommendations for Prehospital Stroke Care Associated with Shorter Door-to-CT Times - an analysis of Get with the Guidelines-Stroke registry and prehospital dataLayne Dylla, Hannah M Higgins, Courtney D Wham, et al.
Human Molecular Genetics|June 1, 1992
Genetic linkage of the human gene for phenylethanolamine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21-q22M R Hoehe, R Plaetke, B Otterud, et al.
Genomics|February 10, 1995
Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22.1C A Klanke, Y R Su, D F Callen, et al.
Nature|April 5, 1990
Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3L M Brzustowicz, T Lehner, L H Castilla, et al.
Pageof 131

Showing results (931-940 of 1,307) with videos related to

Sort By:
Pageof 131
Circulation|October 16, 2025
Opportunistic Detection of Coronary Artery Calcium on Noncardiac Chest Computed Tomography: An Emerging Tool for Cardiovascular Disease Prevention: A Scientific Statement From the American Heart AssociationRandi Foraker, Laurence Sperling, Lisa Bratzke, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 3, 2021
Osteoporosis, Fractures, and Bone Mineral Density Screening in Veterans With Kidney Stone DiseaseCalyani Ganesan, I-Chun Thomas, Ruth Romero, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|July 18, 2022
Minocycline treatment in clinically isolated syndrome and serum NfL, GFAP, and metalloproteinase levelsCarlos Camara-Lemarroy, Luanne Metz, Jens Kuhle, et al.
Cancer Research|November 11, 1998
The inducible prostaglandin biosynthetic enzyme, cyclooxygenase 2, is not mutated in patients with attenuated adenomatous polyposis coliL N Spirio, D A Dixon, J Robertson, et al.
Developmental Medicine and Child Neurology|June 4, 1999
Sequential neuromotor examination in children with intrauterine cocaine/polydrug exposureH M Belcher, B K Shapiro, M Leppert, et al.
Nature Communications|February 12, 2020
Serum neurofilament light levels in normal aging and their association with morphologic brain changesMichael Khalil, Lukas Pirpamer, Edith Hofer, et al.
Frontiers in Stroke|July 25, 2025
Identification of Specific Recommendations for Prehospital Stroke Care Associated with Shorter Door-to-CT Times - an analysis of Get with the Guidelines-Stroke registry and prehospital dataLayne Dylla, Hannah M Higgins, Courtney D Wham, et al.
Human Molecular Genetics|June 1, 1992
Genetic linkage of the human gene for phenylethanolamine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21-q22M R Hoehe, R Plaetke, B Otterud, et al.
Genomics|February 10, 1995
Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22.1C A Klanke, Y R Su, D F Callen, et al.
Nature|April 5, 1990
Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3L M Brzustowicz, T Lehner, L H Castilla, et al.
Pageof 131