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R Greenberg

Showing results (721-730 of 844) with videos related to

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Diseases of the Colon and Rectum|May 1, 1997
Preliminary report on the Mount Sinai Hospital Inflammatory Bowel Disease Genetics ProjectR S McLeod, A H Steinhart, K A Siminovitch, et al.
Journal of the National Cancer Institute|June 24, 1998
Exposure to breast milk in infancy and adult breast cancer riskL Titus-Ernstoff, K M Egan, P A Newcomb, et al.
Urologic Oncology|January 23, 2024
The association between frailty, hypogonadism, and postoperative outcomes among men undergoing radical cystectomyDaniel R Greenberg, Stephen Rhodes, Hriday P Bhambhvani, et al.
Journal of Surgical Oncology|April 30, 2024
Hypogonadism, frailty, and postoperative outcomes among men undergoing radical nephrectomyDaniel R Greenberg, Stephen P Rhodes, Alon Lazarovich, et al.
Human Molecular Genetics|November 5, 1999
CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasiaG Zhou, Y Chen, L Zhou, et al.
Journal of Clinical Medicine|June 26, 2025
The Impact of a Formalized Fertility Preservation Program on Access to Care and Sperm Cryopreservation Among Transgender and Nonbinary Patients Assigned Male at BirthDaniel R Greenberg, Faraz N Longi, Sarah C Cromack, et al.
Journal of Endocrinological Investigation|February 22, 2024
Novel reference range values for serum testosterone: a cross-sectional study of 200,000 malesRichard J Fantus, Daniel R Greenberg, Cecilia Chang, et al.
The New England Journal of Medicine|May 8, 1998
Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase geneC A Stanley, Y K Lieu, B Y Hsu, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1988
Fludarabine monophosphate: a potentially useful agent in chronic lymphocytic leukemiaM R Grever, K J Kopecky, C A Coltman, et al.
American Journal of Human Genetics|March 31, 2000
Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) geneL B Meira, J M Graham, C R Greenberg, et al.
Pageof 85

Showing results (721-730 of 844) with videos related to

Sort By:
Pageof 85
Diseases of the Colon and Rectum|May 1, 1997
Preliminary report on the Mount Sinai Hospital Inflammatory Bowel Disease Genetics ProjectR S McLeod, A H Steinhart, K A Siminovitch, et al.
Journal of the National Cancer Institute|June 24, 1998
Exposure to breast milk in infancy and adult breast cancer riskL Titus-Ernstoff, K M Egan, P A Newcomb, et al.
Urologic Oncology|January 23, 2024
The association between frailty, hypogonadism, and postoperative outcomes among men undergoing radical cystectomyDaniel R Greenberg, Stephen Rhodes, Hriday P Bhambhvani, et al.
Journal of Surgical Oncology|April 30, 2024
Hypogonadism, frailty, and postoperative outcomes among men undergoing radical nephrectomyDaniel R Greenberg, Stephen P Rhodes, Alon Lazarovich, et al.
Human Molecular Genetics|November 5, 1999
CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasiaG Zhou, Y Chen, L Zhou, et al.
Journal of Clinical Medicine|June 26, 2025
The Impact of a Formalized Fertility Preservation Program on Access to Care and Sperm Cryopreservation Among Transgender and Nonbinary Patients Assigned Male at BirthDaniel R Greenberg, Faraz N Longi, Sarah C Cromack, et al.
Journal of Endocrinological Investigation|February 22, 2024
Novel reference range values for serum testosterone: a cross-sectional study of 200,000 malesRichard J Fantus, Daniel R Greenberg, Cecilia Chang, et al.
The New England Journal of Medicine|May 8, 1998
Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase geneC A Stanley, Y K Lieu, B Y Hsu, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1988
Fludarabine monophosphate: a potentially useful agent in chronic lymphocytic leukemiaM R Grever, K J Kopecky, C A Coltman, et al.
American Journal of Human Genetics|March 31, 2000
Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) geneL B Meira, J M Graham, C R Greenberg, et al.
Pageof 85