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M G Vogiatzi

Showing results (1-10 of 13) with videos related to

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Pediatrics in Review|March 24, 1998
The short childM G Vogiatzi, K C Copeland
Pediatrics|April 3, 1998
Frequency and necessity of thyroid function tests in neonates and infants with congenital hypothyroidismM G Vogiatzi, J L Kirkland
The Journal of Clinical Endocrinology and Metabolism|July 10, 2001
Long term outcome in adult males with classic congenital adrenal hyperplasiaM S Cabrera, M G Vogiatzi, M I New
The Journal of Clinical Endocrinology and Metabolism|December 17, 1997
Insulin does not stimulate protein synthesis acutely in prepubertal children with insulin-dependent diabetes mellitusM G Vogiatzi, K S Nair, P R Beckett, et al.
Clinical Pediatrics|July 1, 1996
Gastrointestinal symptoms and diabetes mellitus in children and adolescentsM G Vogiatzi, S K Gunn, L D Sherman, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2001
Growth hormone therapy alone or in combination with gonadotropin-releasing hormone analog therapy to improve the height deficit in children with congenital adrenal hyperplasiaJ B Quintos, M G Vogiatzi, M D Harbison, et al.
Metabolism: Clinical and Experimental|August 1, 1996
Dehydroepiandrosterone in morbidly obese adolescents: effects on weight, body composition, lipids, and insulin resistanceM G Vogiatzi, M A Boeck, E Vlachopapadopoulou, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1995
Adrenal crisis in the newborn: details leading to the correct diagnosisM G Vogiatzi, S K Gunn, A E Scheuerle, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|December 10, 2015
Polycythemia is associated with bone loss and reduced osteoblast activity in miceP R Oikonomidou, C Casu, Z Yang, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|October 4, 2017
A novel dominant COL11A1 mutation in a child with Stickler syndrome type II is associated with recurrent fracturesM G Vogiatzi, D Li, L Tian, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Pediatrics in Review|March 24, 1998
The short childM G Vogiatzi, K C Copeland
Pediatrics|April 3, 1998
Frequency and necessity of thyroid function tests in neonates and infants with congenital hypothyroidismM G Vogiatzi, J L Kirkland
The Journal of Clinical Endocrinology and Metabolism|July 10, 2001
Long term outcome in adult males with classic congenital adrenal hyperplasiaM S Cabrera, M G Vogiatzi, M I New
The Journal of Clinical Endocrinology and Metabolism|December 17, 1997
Insulin does not stimulate protein synthesis acutely in prepubertal children with insulin-dependent diabetes mellitusM G Vogiatzi, K S Nair, P R Beckett, et al.
Clinical Pediatrics|July 1, 1996
Gastrointestinal symptoms and diabetes mellitus in children and adolescentsM G Vogiatzi, S K Gunn, L D Sherman, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2001
Growth hormone therapy alone or in combination with gonadotropin-releasing hormone analog therapy to improve the height deficit in children with congenital adrenal hyperplasiaJ B Quintos, M G Vogiatzi, M D Harbison, et al.
Metabolism: Clinical and Experimental|August 1, 1996
Dehydroepiandrosterone in morbidly obese adolescents: effects on weight, body composition, lipids, and insulin resistanceM G Vogiatzi, M A Boeck, E Vlachopapadopoulou, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1995
Adrenal crisis in the newborn: details leading to the correct diagnosisM G Vogiatzi, S K Gunn, A E Scheuerle, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|December 10, 2015
Polycythemia is associated with bone loss and reduced osteoblast activity in miceP R Oikonomidou, C Casu, Z Yang, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|October 4, 2017
A novel dominant COL11A1 mutation in a child with Stickler syndrome type II is associated with recurrent fracturesM G Vogiatzi, D Li, L Tian, et al.
Pageof 2