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A Ganguly

Showing results (151-160 of 168) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|November 1, 1984
Elevated urinary excretion of 18-oxocortisol in glucocorticoid-suppressible aldosteronismC E Gomez-Sanchez, M Montgomery, A Ganguly, et al.
AJNR. American Journal of Neuroradiology|July 16, 2011
Cerebral CT perfusion using an interventional C-arm imaging system: cerebral blood flow measurementsA Ganguly, A Fieselmann, M Marks, et al.
Molecular Genetics and Metabolism|October 11, 2001
Aberrant mRNA splicing associated with coding region mutations in children with carnitine-acylcarnitine translocase deficiencyB Y Hsu, V Iacobazzi, Z Wang, et al.
The New England Journal of Medicine|May 15, 1997
BRCA1 mutations in women attending clinics that evaluate the risk of breast cancerF J Couch, M L DeShano, M A Blackwood, et al.
Metabolism: Clinical and Experimental|June 1, 1982
The renin-angiotensin-aldosterone system and hypertension in primary hyperparathyroidismA Ganguly, M H Weinberger, J M Passmore, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 2013
Genotype and phenotype correlations in 417 children with congenital hyperinsulinismK E Snider, S Becker, L Boyajian, et al.
Matrix (Stuttgart, Germany)|April 1, 1992
Three new polymorphisms at the COL1A2 locusD Strobel, T Tsuneyoshi, H Kuivaniemi, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2001
Hyperinsulinism/hyperammonemia syndrome in children with regulatory mutations in the inhibitory guanosine triphosphate-binding domain of glutamate dehydrogenaseC MacMullen, J Fang, B Y Hsu, et al.
Annals of Internal Medicine|March 1, 1979
Primary aldosteronism: diagnosis, localization, and treatmentM H Weinberger, C E Grim, J W Hollifield, et al.
Nature Genetics|September 11, 1992
Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthaseR P Lifton, R G Dluhy, M Powers, et al.
Pageof 17

Showing results (151-160 of 168) with videos related to

Sort By:
Pageof 17
The Journal of Clinical Endocrinology and Metabolism|November 1, 1984
Elevated urinary excretion of 18-oxocortisol in glucocorticoid-suppressible aldosteronismC E Gomez-Sanchez, M Montgomery, A Ganguly, et al.
AJNR. American Journal of Neuroradiology|July 16, 2011
Cerebral CT perfusion using an interventional C-arm imaging system: cerebral blood flow measurementsA Ganguly, A Fieselmann, M Marks, et al.
Molecular Genetics and Metabolism|October 11, 2001
Aberrant mRNA splicing associated with coding region mutations in children with carnitine-acylcarnitine translocase deficiencyB Y Hsu, V Iacobazzi, Z Wang, et al.
The New England Journal of Medicine|May 15, 1997
BRCA1 mutations in women attending clinics that evaluate the risk of breast cancerF J Couch, M L DeShano, M A Blackwood, et al.
Metabolism: Clinical and Experimental|June 1, 1982
The renin-angiotensin-aldosterone system and hypertension in primary hyperparathyroidismA Ganguly, M H Weinberger, J M Passmore, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 2013
Genotype and phenotype correlations in 417 children with congenital hyperinsulinismK E Snider, S Becker, L Boyajian, et al.
Matrix (Stuttgart, Germany)|April 1, 1992
Three new polymorphisms at the COL1A2 locusD Strobel, T Tsuneyoshi, H Kuivaniemi, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2001
Hyperinsulinism/hyperammonemia syndrome in children with regulatory mutations in the inhibitory guanosine triphosphate-binding domain of glutamate dehydrogenaseC MacMullen, J Fang, B Y Hsu, et al.
Annals of Internal Medicine|March 1, 1979
Primary aldosteronism: diagnosis, localization, and treatmentM H Weinberger, C E Grim, J W Hollifield, et al.
Nature Genetics|September 11, 1992
Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthaseR P Lifton, R G Dluhy, M Powers, et al.
Pageof 17