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J C Achermann

Showing results (11-20 of 28) with videos related to

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Journal of Pediatric Urology|April 27, 2013
Persistent unexplained congenital clitoromegaly in females born extremely prematurelyC E Williams, R S Nakhal, J C Achermann, et al.
The Journal of Pediatrics|December 13, 2000
Presymptomatic diagnosis of X-linked adrenal hypoplasia congenita by analysis of DAX1J C Achermann, B L Silverman, R L Habiby, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 11, 2001
Variable presentation of X-linked adrenal hypoplasia congenitaE Wiltshire, J Couper, C Rodda, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 8, 2010
New technologies for the identification of novel genetic markers of disorders of sex development (DSD)A Bashamboo, S Ledig, P Wieacker, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
X-linked adrenal hypoplasia congenita: a mutation in DAX1 expands the phenotypic spectrum in males and femalesS B Seminara, J C Achermann, M Genel, et al.
Clinical Endocrinology|December 14, 1999
The relative roles of continuous growth hormone-releasing hormone (GHRH(1-29)NH2) and intermittent somatostatin(1-14)(SS) in growth hormone (GH) pulse generation: studies in normal and post cranial irradiated individualsJ C Achermann, P C Hindmarsh, I C Robinson, et al.
Clinical Endocrinology|August 6, 1999
Peak and trough growth hormone (GH) concentrations influence growth and serum insulin like growth factor-1 (IGF-1) concentrations in short childrenJ C Achermann, C G Brook, I C Robinson, et al.
Journal of Pediatric Urology|January 28, 2012
Clinical and gonadal features and early surgical management of 45,X/46,XY and 45,X/47,XYY chromosomal mosaicism presenting with genital anomaliesM K Farrugia, N J Sebire, J C Achermann, et al.
The Journal of Clinical Endocrinology and Metabolism|July 10, 2001
Missense mutations cluster within the carboxyl-terminal region of DAX-1 and impair transcriptional repressionJ C Achermann, M Ito, B L Silverman, et al.
Molecular Genetics and Metabolism|August 18, 2001
Molecular and structural analysis of two novel StAR mutations in patients with lipoid congenital adrenal hyperplasiaJ C Achermann, J J Meeks, B Jeffs, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Journal of Pediatric Urology|April 27, 2013
Persistent unexplained congenital clitoromegaly in females born extremely prematurelyC E Williams, R S Nakhal, J C Achermann, et al.
The Journal of Pediatrics|December 13, 2000
Presymptomatic diagnosis of X-linked adrenal hypoplasia congenita by analysis of DAX1J C Achermann, B L Silverman, R L Habiby, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 11, 2001
Variable presentation of X-linked adrenal hypoplasia congenitaE Wiltshire, J Couper, C Rodda, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 8, 2010
New technologies for the identification of novel genetic markers of disorders of sex development (DSD)A Bashamboo, S Ledig, P Wieacker, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
X-linked adrenal hypoplasia congenita: a mutation in DAX1 expands the phenotypic spectrum in males and femalesS B Seminara, J C Achermann, M Genel, et al.
Clinical Endocrinology|December 14, 1999
The relative roles of continuous growth hormone-releasing hormone (GHRH(1-29)NH2) and intermittent somatostatin(1-14)(SS) in growth hormone (GH) pulse generation: studies in normal and post cranial irradiated individualsJ C Achermann, P C Hindmarsh, I C Robinson, et al.
Clinical Endocrinology|August 6, 1999
Peak and trough growth hormone (GH) concentrations influence growth and serum insulin like growth factor-1 (IGF-1) concentrations in short childrenJ C Achermann, C G Brook, I C Robinson, et al.
Journal of Pediatric Urology|January 28, 2012
Clinical and gonadal features and early surgical management of 45,X/46,XY and 45,X/47,XYY chromosomal mosaicism presenting with genital anomaliesM K Farrugia, N J Sebire, J C Achermann, et al.
The Journal of Clinical Endocrinology and Metabolism|July 10, 2001
Missense mutations cluster within the carboxyl-terminal region of DAX-1 and impair transcriptional repressionJ C Achermann, M Ito, B L Silverman, et al.
Molecular Genetics and Metabolism|August 18, 2001
Molecular and structural analysis of two novel StAR mutations in patients with lipoid congenital adrenal hyperplasiaJ C Achermann, J J Meeks, B Jeffs, et al.
Pageof 3