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Diseases of the Colon and Rectum
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May 1, 1997
Preliminary report on the Mount Sinai Hospital Inflammatory Bowel Disease Genetics Project
R 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 risk
L 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 cystectomy
Daniel 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 nephrectomy
Daniel 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 dysplasia
G 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 Birth
Daniel 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 males
Richard 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 gene
C 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 leukemia
M 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) gene
L B Meira, J M Graham, C R Greenberg, et al.
Page
of 85
Search research articles
Search
Showing results (721-730 of 844) with videos related to
Sort By:
Page
of 85
Diseases of the Colon and Rectum
|
May 1, 1997
Preliminary report on the Mount Sinai Hospital Inflammatory Bowel Disease Genetics Project
R 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 risk
L 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 cystectomy
Daniel 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 nephrectomy
Daniel 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 dysplasia
G 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 Birth
Daniel 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 males
Richard 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 gene
C 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 leukemia
M 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) gene
L B Meira, J M Graham, C R Greenberg, et al.
Page
of 85