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P Kopp

Showing results (171-180 of 214) with videos related to

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The Journal of Urology|March 20, 2018
Unconventional Bladder Preservation: Factors Predicting Failure to Receive Definitive Surgery following Chemotherapy for Nonmetastatic Muscle Invasive Bladder Cancer in the National Cancer DatabaseAkash A Kapadia, Ann Martinez Acevedo, Jen-Jane Liu, et al.
JAMA Surgery|March 19, 2020
Association Between American Board of Surgery Initial Certification and Risk of Receiving Severe Disciplinary Actions Against Medical LicensesJason P Kopp, Beatriz Ibáñez, Andrew T Jones, et al.
Journal of Thrombosis and Haemostasis : JTH|January 28, 2010
Thrombin generation in morbid obesity: significant reduction after weight lossL Ay, H-P Kopp, J-M Brix, et al.
Alcohol (Fayetteville, N.Y.)|January 1, 1986
Frequencies of glyoxalase I phenotypes as biological markers in chronic alcoholismM Ledig, M Doffoel, M Ziessel, et al.
JAMA Surgery|November 7, 2019
Association Between Resident Physician Training Experience and Program-Level Performance on Board ExaminationsRyan J Ellis, Yue-Yung Hu, Andrew T Jones, et al.
Urology|November 7, 2016
Bilateral Testicular Germ Cell Tumors in the Era of Multimodal TherapyRyan P Kopp, Michael Chevinsky, Melanie Bernstein, et al.
Cancer|February 8, 2017
Utility of prospective pathologic evaluation to inform clinical genetic testing for hereditary leiomyomatosis and renal cell carcinomaRyan P Kopp, Kelly L Stratton, Emily Glogowski, et al.
Journal of Endocrinological Investigation|August 12, 1998
Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindredC R Nogueira, C C Leite, E P Chedid, et al.
Journal of Endocrinological Investigation|January 24, 1998
Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindredC R Nogueira, C C Leite, E P Chedid, et al.
Endocrinology|July 1, 1995
The thyrotropin (TSH) receptor transmembrane domain mutation (Pro556-Leu) in the hypothyroid hyt/hyt mouse results in plasma membrane targeting but defective TSH bindingW X Gu, G G Du, P Kopp, et al.
Pageof 22

Showing results (171-180 of 214) with videos related to

Sort By:
Pageof 22
The Journal of Urology|March 20, 2018
Unconventional Bladder Preservation: Factors Predicting Failure to Receive Definitive Surgery following Chemotherapy for Nonmetastatic Muscle Invasive Bladder Cancer in the National Cancer DatabaseAkash A Kapadia, Ann Martinez Acevedo, Jen-Jane Liu, et al.
JAMA Surgery|March 19, 2020
Association Between American Board of Surgery Initial Certification and Risk of Receiving Severe Disciplinary Actions Against Medical LicensesJason P Kopp, Beatriz Ibáñez, Andrew T Jones, et al.
Journal of Thrombosis and Haemostasis : JTH|January 28, 2010
Thrombin generation in morbid obesity: significant reduction after weight lossL Ay, H-P Kopp, J-M Brix, et al.
Alcohol (Fayetteville, N.Y.)|January 1, 1986
Frequencies of glyoxalase I phenotypes as biological markers in chronic alcoholismM Ledig, M Doffoel, M Ziessel, et al.
JAMA Surgery|November 7, 2019
Association Between Resident Physician Training Experience and Program-Level Performance on Board ExaminationsRyan J Ellis, Yue-Yung Hu, Andrew T Jones, et al.
Urology|November 7, 2016
Bilateral Testicular Germ Cell Tumors in the Era of Multimodal TherapyRyan P Kopp, Michael Chevinsky, Melanie Bernstein, et al.
Cancer|February 8, 2017
Utility of prospective pathologic evaluation to inform clinical genetic testing for hereditary leiomyomatosis and renal cell carcinomaRyan P Kopp, Kelly L Stratton, Emily Glogowski, et al.
Journal of Endocrinological Investigation|August 12, 1998
Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindredC R Nogueira, C C Leite, E P Chedid, et al.
Journal of Endocrinological Investigation|January 24, 1998
Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindredC R Nogueira, C C Leite, E P Chedid, et al.
Endocrinology|July 1, 1995
The thyrotropin (TSH) receptor transmembrane domain mutation (Pro556-Leu) in the hypothyroid hyt/hyt mouse results in plasma membrane targeting but defective TSH bindingW X Gu, G G Du, P Kopp, et al.
Pageof 22