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A Ganguly

Showing results (121-130 of 168) with videos related to

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The Journal of Urology|December 1, 1981
Hyperaldosteronism due to unsuspected adrenal carcinoma: discovery during investigation of hypertension in a young womanC E Grim, A Ganguly, M N Yum, et al.
The American Journal of Medicine|February 1, 1976
Cushing's syndrome in a patient with an empty sella turcica and a microadenoma of the adenohypophysisA Ganguly, J B Stanchfield, T S Roberts, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1983
Differing effects of metoclopramide and adrenocorticotropin on plasma aldosterone levels in glucocorticoid-suppressible hyperaldosteronism and other forms of hyperaldosteronismA Ganguly, J H Pratt, M H Weinberger, et al.
The New England Journal of Medicine|September 6, 1979
Computerized tomographic scanning and primary aldosteronismA Ganguly, J H Pratt, H Y Yune, et al.
Annals of the Royal College of Surgeons of England|July 29, 2010
The benefits of on-site cytology with ultrasound-guided fine needle aspiration in a one-stop neck lump clinicA Ganguly, T E Giles, P A Smith, et al.
Archives of Internal Medicine|May 1, 1979
Detection of adrenal tumors by computerized tomographic scan in endocrine hypertensionA Ganguly, J H Pratt, H Y Yune, et al.
Journal of Steroid Biochemistry|March 1, 1989
18-oxocortisol: effect of dexamethasone, ACTH and sodium restrictionC E Gomez-Sanchez, P G Zager, M F Foecking, et al.
Indian Journal of Pathology & Microbiology|December 1, 1994
Bombay 'O' group blood (Oh phenotype) in two subjects in a family at CalcuttaS Chakraborty, V N Bhatia, B Mukherjee, et al.
Pediatric Blood & Cancer|July 31, 2025
Increasing Paternal Age Associated With Elevated Risk of De Novo Mutations in Offspring Diagnosed With Sporadic Bilateral RetinoblastomaMaral Adel Fahmideh, Arupa A Ganguly, Tiffany M Chambers, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 15, 1991
Mutation in a gene for type I procollagen (COL1A2) in a woman with postmenopausal osteoporosis: evidence for phenotypic and genotypic overlap with mild osteogenesis imperfectaL D Spotila, C D Constantinou, L Sereda, et al.
Pageof 17

Showing results (121-130 of 168) with videos related to

Sort By:
Pageof 17
The Journal of Urology|December 1, 1981
Hyperaldosteronism due to unsuspected adrenal carcinoma: discovery during investigation of hypertension in a young womanC E Grim, A Ganguly, M N Yum, et al.
The American Journal of Medicine|February 1, 1976
Cushing's syndrome in a patient with an empty sella turcica and a microadenoma of the adenohypophysisA Ganguly, J B Stanchfield, T S Roberts, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1983
Differing effects of metoclopramide and adrenocorticotropin on plasma aldosterone levels in glucocorticoid-suppressible hyperaldosteronism and other forms of hyperaldosteronismA Ganguly, J H Pratt, M H Weinberger, et al.
The New England Journal of Medicine|September 6, 1979
Computerized tomographic scanning and primary aldosteronismA Ganguly, J H Pratt, H Y Yune, et al.
Annals of the Royal College of Surgeons of England|July 29, 2010
The benefits of on-site cytology with ultrasound-guided fine needle aspiration in a one-stop neck lump clinicA Ganguly, T E Giles, P A Smith, et al.
Archives of Internal Medicine|May 1, 1979
Detection of adrenal tumors by computerized tomographic scan in endocrine hypertensionA Ganguly, J H Pratt, H Y Yune, et al.
Journal of Steroid Biochemistry|March 1, 1989
18-oxocortisol: effect of dexamethasone, ACTH and sodium restrictionC E Gomez-Sanchez, P G Zager, M F Foecking, et al.
Indian Journal of Pathology & Microbiology|December 1, 1994
Bombay 'O' group blood (Oh phenotype) in two subjects in a family at CalcuttaS Chakraborty, V N Bhatia, B Mukherjee, et al.
Pediatric Blood & Cancer|July 31, 2025
Increasing Paternal Age Associated With Elevated Risk of De Novo Mutations in Offspring Diagnosed With Sporadic Bilateral RetinoblastomaMaral Adel Fahmideh, Arupa A Ganguly, Tiffany M Chambers, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 15, 1991
Mutation in a gene for type I procollagen (COL1A2) in a woman with postmenopausal osteoporosis: evidence for phenotypic and genotypic overlap with mild osteogenesis imperfectaL D Spotila, C D Constantinou, L Sereda, et al.
Pageof 17