Search Results - "Stanhope, Richard G."

Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization by Quinton, Richard, Duke, Véronique M., Robertson, Alexis, Kirk, Jeremy M. W., Matfin, Glenn, De Zoysa, Priyal A., Azcona, Christina, MacColl, Gavin S., Jacobs, Howard S., Conway, Gerard S., Besser, Michael, Stanhope, Richard G., Bouloux, Pierre-Marc G.

“…OBJECTIVE The association of idiopathic hypogonadotrophic hypogonadism (IHH) with congenital olfactory deficit defines Kallmann's syndrome (KS). Although a…”
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Is the Thyrotropin-Releasing Hormone Test Necessary in the Diagnosis of Central Hypothyroidism in Children by Mehta, Ameeta, Hindmarsh, Peter C., Stanhope, Richard G., Brain, Caroline E., Preece, Michael A., Dattani, Mehul T.

“…To determine the value of the TRH test, we analyzed the unstimulated serum T4 and TSH concentrations in 54 children with central hypothyroidism. A TRH test was…”
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Phenotypic variability in 17β-hydroxysteroid dehydrogenase-3 deficiency and diagnostic pitfalls by Lee, Yung Seng, Kirk, Jeremy M. W., Stanhope, Richard G., Johnston, Derek I., Harland, Sharon, Auchus, Richard J., Andersson, Stefan, Hughes, Ieuan A.

“…Summary Objective  17β‐hydroxysteroid dehydrogenase type 3 isoenzyme (17β‐HSD3) is required to produce testosterone for male sex differentiation. Mutations in…”
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A frameshift mutation in MC4R associated with dominantly inherited human obesity by O'Rahilly, Stephen, Yeo, Giles S.H, Farooqi, I. Sadaf, Aminian, Shiva, Halsall, David J, Stanhope, Richard G

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The role of growth hormone in determining birth size and early postnatal growth, using congenital growth hormone deficiency (GHD) as a model by Mehta, Ameeta, Hindmarsh, Peter C., Stanhope, Richard G., Turton, James P. G., Cole, Tim J., Preece, Michael A., Dattani, Mehul T.

“…Summary Objective  The role of GH in early human growth is unclear. Congenital GH deficiency (CGHD) provides a useful tool to explore this putative role. We…”
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Routine neuroimaging in classical isolated gonadotrophin deficiency is of limited clinical value by Quinton, Richard, Beirne, Paul, Bouloux, Pierre-M. G., Stanhope, Richard G., Conway, Gerard S.

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Phenotypic variability in 17beta-hydroxysteroid dehydrogenase-3 deficiency and diagnostic pitfalls by Lee, Yung Seng, Kirk, Jeremy M W, Stanhope, Richard G, Johnston, Derek I, Harland, Sharon, Auchus, Richard J, Andersson, Stefan, Hughes, Ieuan A

“…17beta-hydroxysteroid dehydrogenase type 3 isoenzyme (17beta-HSD3) is required to produce testosterone for male sex differentiation. Mutations in the HSD17B3…”
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Quality of life and psychological outcome in patients treated for craniopharyngioma by Toumba, Meropi, Stanhope, Richard

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