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Peter C Hindmarsh

Showing results (81-90 of 93) with videos related to

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BMJ (Clinical Research Ed.)|April 16, 2011
Effect of oxandrolone and timing of pubertal induction on final height in Turner's syndrome: randomised, double blind, placebo controlled trialEmma Jane Gault, Rebecca J Perry, Tim J Cole, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|July 28, 2016
No relationship between prenatal androgen exposure and autistic traits: convergent evidence from studies of children with congenital adrenal hyperplasia and of amniotic testosterone concentrations in typically developing childrenKarson T F Kung, Debra Spencer, Vickie Pasterski, et al.
Clinical Endocrinology|January 17, 2007
Severe loss-of-function mutations in the adrenocorticotropin receptor (ACTHR, MC2R) can be found in patients diagnosed with salt-losing adrenal hypoplasiaLin Lin, Peter C Hindmarsh, Louise A Metherell, et al.
American Journal of Human Genetics|March 27, 2012
Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weightMiho Ishida, David Monk, Andrew J Duncan, et al.
Clinical Endocrinology|October 27, 2011
Association of the (CA)n repeat polymorphism of insulin-like growth factor-I and -202 A/C IGF-binding protein-3 promoter polymorphism with adult height in patients with severe growth hormone deficiencyMaria Consolata Miletta, Ursina A Scheidegger, Mara Giordano, et al.
Clinical Endocrinology|June 21, 2005
Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD)James P G Turton, Ameeta Mehta, Jamal Raza, et al.
Archives of Disease in Childhood|April 12, 2023
Emergency and perioperative management of adrenal insufficiency in children and young people: British Society for Paediatric Endocrinology and Diabetes consensus guidanceTalat Mushtaq, Salma R Ali, Nabil Boulos, et al.
The Journal of Clinical Endocrinology and Metabolism|July 2, 2009
Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiencyKyriaki S Alatzoglou, James P Turton, Daniel Kelberman, et al.
Journal of the Endocrine Society|November 24, 2022
A Single-Center, Observational Study of 607 Children and Young People Presenting With Differences of Sex Development (DSD)Elim Man, Imran Mushtaq, Angela Barnicoat, et al.
Cell|November 12, 2013
KSR2 mutations are associated with obesity, insulin resistance, and impaired cellular fuel oxidationLaura R Pearce, Neli Atanassova, Matthew C Banton, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
BMJ (Clinical Research Ed.)|April 16, 2011
Effect of oxandrolone and timing of pubertal induction on final height in Turner's syndrome: randomised, double blind, placebo controlled trialEmma Jane Gault, Rebecca J Perry, Tim J Cole, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|July 28, 2016
No relationship between prenatal androgen exposure and autistic traits: convergent evidence from studies of children with congenital adrenal hyperplasia and of amniotic testosterone concentrations in typically developing childrenKarson T F Kung, Debra Spencer, Vickie Pasterski, et al.
Clinical Endocrinology|January 17, 2007
Severe loss-of-function mutations in the adrenocorticotropin receptor (ACTHR, MC2R) can be found in patients diagnosed with salt-losing adrenal hypoplasiaLin Lin, Peter C Hindmarsh, Louise A Metherell, et al.
American Journal of Human Genetics|March 27, 2012
Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weightMiho Ishida, David Monk, Andrew J Duncan, et al.
Clinical Endocrinology|October 27, 2011
Association of the (CA)n repeat polymorphism of insulin-like growth factor-I and -202 A/C IGF-binding protein-3 promoter polymorphism with adult height in patients with severe growth hormone deficiencyMaria Consolata Miletta, Ursina A Scheidegger, Mara Giordano, et al.
Clinical Endocrinology|June 21, 2005
Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD)James P G Turton, Ameeta Mehta, Jamal Raza, et al.
Archives of Disease in Childhood|April 12, 2023
Emergency and perioperative management of adrenal insufficiency in children and young people: British Society for Paediatric Endocrinology and Diabetes consensus guidanceTalat Mushtaq, Salma R Ali, Nabil Boulos, et al.
The Journal of Clinical Endocrinology and Metabolism|July 2, 2009
Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiencyKyriaki S Alatzoglou, James P Turton, Daniel Kelberman, et al.
Journal of the Endocrine Society|November 24, 2022
A Single-Center, Observational Study of 607 Children and Young People Presenting With Differences of Sex Development (DSD)Elim Man, Imran Mushtaq, Angela Barnicoat, et al.
Cell|November 12, 2013
KSR2 mutations are associated with obesity, insulin resistance, and impaired cellular fuel oxidationLaura R Pearce, Neli Atanassova, Matthew C Banton, et al.
Pageof 10