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Svetlana Ten

Showing results (31-40 of 56) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|August 25, 2005
Phenotypic features associated with mutations in steroidogenic acute regulatory proteinAmrit Bhangoo, Wen-Xia Gu, Steven Pavlakis, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 22, 2008
Novel mutation in cytochrome P450c17 causes complete combined 17alpha-hydroxylase/17,20-lyase deficiencyAmrit Bhangoo, Javier Aisenberg, Amy Chartoffe, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 18, 2008
Resting energy expenditure in insulin resistance falls with decompensation of insulin secretion in obese childrenSvetlana Ten, Amrit Bhangoo, Neesha Ramchandani, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 28, 2007
Effect of metformin and rosiglitazone in a prepubertal boy with Alström syndromeSunil K Sinha, Amrit Bhangoo, Henry Anhalt, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|January 11, 2011
Isolated mild clitoral hypertrophy may reveal 46,XY disorders of sex development in infancy due to 17βHSD-3 defect confirmed by molecular analysisMinu M George, Sunil Sinha, Irene Mamkin, et al.
The Journal of Clinical Endocrinology and Metabolism|August 9, 2012
Role of 11βHSD type 2 enzyme activity in essential hypertension and children with chronic kidney disease (CKD)Anil Mongia, Risa Vecker, Minu George, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 8, 2012
The prevalence of non-alcoholic fatty liver disease and metabolic syndrome in obese childrenRishi Gupta, Amrit Bhangoo, Nicole A V Matthews, et al.
The Journal of Clinical Endocrinology and Metabolism|January 6, 2006
Clinical case seminar: a novel LHX3 mutation presenting as combined pituitary hormonal deficiencyAmrit P S Bhangoo, Chad S Hunter, Jesse J Savage, et al.
International Journal of Pediatric Endocrinology|October 15, 2011
Unique phenotype in a patient with CHARGE syndromeShobhit Jain, Hyung-Goo Kim, Felicitas Lacbawan, et al.
The Journal of Clinical Investigation|January 10, 2002
Multiple immuno-regulatory defects in type-1 diabetesAnjli Kukreja, Giulia Cost, John Marker, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

Sort By:
Pageof 6
The Journal of Clinical Endocrinology and Metabolism|August 25, 2005
Phenotypic features associated with mutations in steroidogenic acute regulatory proteinAmrit Bhangoo, Wen-Xia Gu, Steven Pavlakis, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 22, 2008
Novel mutation in cytochrome P450c17 causes complete combined 17alpha-hydroxylase/17,20-lyase deficiencyAmrit Bhangoo, Javier Aisenberg, Amy Chartoffe, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 18, 2008
Resting energy expenditure in insulin resistance falls with decompensation of insulin secretion in obese childrenSvetlana Ten, Amrit Bhangoo, Neesha Ramchandani, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 28, 2007
Effect of metformin and rosiglitazone in a prepubertal boy with Alström syndromeSunil K Sinha, Amrit Bhangoo, Henry Anhalt, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|January 11, 2011
Isolated mild clitoral hypertrophy may reveal 46,XY disorders of sex development in infancy due to 17βHSD-3 defect confirmed by molecular analysisMinu M George, Sunil Sinha, Irene Mamkin, et al.
The Journal of Clinical Endocrinology and Metabolism|August 9, 2012
Role of 11βHSD type 2 enzyme activity in essential hypertension and children with chronic kidney disease (CKD)Anil Mongia, Risa Vecker, Minu George, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 8, 2012
The prevalence of non-alcoholic fatty liver disease and metabolic syndrome in obese childrenRishi Gupta, Amrit Bhangoo, Nicole A V Matthews, et al.
The Journal of Clinical Endocrinology and Metabolism|January 6, 2006
Clinical case seminar: a novel LHX3 mutation presenting as combined pituitary hormonal deficiencyAmrit P S Bhangoo, Chad S Hunter, Jesse J Savage, et al.
International Journal of Pediatric Endocrinology|October 15, 2011
Unique phenotype in a patient with CHARGE syndromeShobhit Jain, Hyung-Goo Kim, Felicitas Lacbawan, et al.
The Journal of Clinical Investigation|January 10, 2002
Multiple immuno-regulatory defects in type-1 diabetesAnjli Kukreja, Giulia Cost, John Marker, et al.
Pageof 6