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G B Cutler

Showing results (31-40 of 268) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|January 1, 1993
Treatment of familial male precocious puberty with spironolactone, testolactone, and deslorelinL Laue, J Jones, K M Barnes, et al.
The Journal of Pediatrics|January 1, 1996
Thyroid abnormalities in children infected with human immunodeficiency virusS Hirschfeld, L Laue, G B Cutler, et al.
The New England Journal of Medicine|April 22, 1999
Hypogonadotropic hypogonadism in a female caused by an X-linked recessive mutation in the DAX1 geneD P Merke, T Tajima, J Baron, et al.
Annals of Internal Medicine|February 1, 1995
Pituitary tumor hemorrhage in Cushing diseaseL B Mercado-Asis, E H Oldfield, G B Cutler
The Journal of Pediatrics|October 1, 1990
Growth and neuroendocrine dysfunction in children with acquired immunodeficiency syndromeL Laue, P A Pizzo, K Butler, et al.
Annals of Internal Medicine|August 1, 1982
Late-onset 21-hydroxylase deficiencyG P Chrousos, A Munabi, G B Cutler, et al.
Radiology|November 1, 1984
Pituitary and ovarian abnormalities demonstrated by CT and ultrasound in children with features of the McCune-Albright syndromeK G Rieth, F Comite, T H Shawker, et al.
The Journal of Clinical Endocrinology and Metabolism|October 13, 1998
A randomized, cross-over trial of once-daily versus twice-daily parathyroid hormone 1-34 in treatment of hypoparathyroidismK K Winer, J A Yanovski, B Sarani, et al.
The Journal of Pediatrics|January 1, 1985
Effect of hydrocortisone dose schedule on adrenal steroid secretion in congenital adrenal hyperplasiaJ Winterer, G P Chrousos, D L Loriaux, et al.
Hormone Research|July 1, 1982
Late-onset 21-hydroxylase deficiency is an allelic variant of congenital adrenal hyperplasia characterized by attenuated clinical expression and different HLA haplotype associationsG P Chrousos, D L Loriaux, D Mann, et al.
Pageof 27

Showing results (31-40 of 268) with videos related to

Sort By:
Pageof 27
The Journal of Clinical Endocrinology and Metabolism|January 1, 1993
Treatment of familial male precocious puberty with spironolactone, testolactone, and deslorelinL Laue, J Jones, K M Barnes, et al.
The Journal of Pediatrics|January 1, 1996
Thyroid abnormalities in children infected with human immunodeficiency virusS Hirschfeld, L Laue, G B Cutler, et al.
The New England Journal of Medicine|April 22, 1999
Hypogonadotropic hypogonadism in a female caused by an X-linked recessive mutation in the DAX1 geneD P Merke, T Tajima, J Baron, et al.
Annals of Internal Medicine|February 1, 1995
Pituitary tumor hemorrhage in Cushing diseaseL B Mercado-Asis, E H Oldfield, G B Cutler
The Journal of Pediatrics|October 1, 1990
Growth and neuroendocrine dysfunction in children with acquired immunodeficiency syndromeL Laue, P A Pizzo, K Butler, et al.
Annals of Internal Medicine|August 1, 1982
Late-onset 21-hydroxylase deficiencyG P Chrousos, A Munabi, G B Cutler, et al.
Radiology|November 1, 1984
Pituitary and ovarian abnormalities demonstrated by CT and ultrasound in children with features of the McCune-Albright syndromeK G Rieth, F Comite, T H Shawker, et al.
The Journal of Clinical Endocrinology and Metabolism|October 13, 1998
A randomized, cross-over trial of once-daily versus twice-daily parathyroid hormone 1-34 in treatment of hypoparathyroidismK K Winer, J A Yanovski, B Sarani, et al.
The Journal of Pediatrics|January 1, 1985
Effect of hydrocortisone dose schedule on adrenal steroid secretion in congenital adrenal hyperplasiaJ Winterer, G P Chrousos, D L Loriaux, et al.
Hormone Research|July 1, 1982
Late-onset 21-hydroxylase deficiency is an allelic variant of congenital adrenal hyperplasia characterized by attenuated clinical expression and different HLA haplotype associationsG P Chrousos, D L Loriaux, D Mann, et al.
Pageof 27