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Publisher: Wiley-Blackwell

Volume 52, Number 5, May 2000

What's best for the bones in Turner syndrome?
pp. 529-530(2)
Author: Hindmarsh

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A longitudinal study on bone mineral density until adulthood in girls with Turner's syndrome participating in a growth hormone injection frequency-response trial
pp. 531-536(6)
Authors: Sas, Theo C.; de Muinck Keizer-Schrama, Sabine M.; Stijnen, Theo; Asarfi, Anjalie; van Leeuwen, Wibeke J.; van Teunenbroek, Arne; van Rijn, Rick R.; Drop, Stenvert L.

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Pre-treatment IGF-I level is the major determinant of GH dosage in adult GH deficiency
pp. 537-542(6)
Authors: Murray; Howell; Lissett; Shalet

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Increase of adhesion molecules, fibrinogen, type-1 plasminogen activator inhibitor and orosomucoid in growth hormone (GH) deficient adults and their modulation by recombinant human GH replacement
pp. 543-548(6)
Authors: Kvasnička, Jan; Marek, Josef; Kvasnička, Tomáš; Weiss, Vladimír; Marková, Markéta; Štìěpán, Jan; Umlaufová, Anna

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Impaired β-cell function in the presence of reduced insulin sensitivity determines glucose tolerance status in acromegalic patients
pp. 549-555(7)
Authors: Kasayama, Soji; Otsuki, Michio; Takagi, Miki; Saito, Hiroshi; Sumitani, Satoru; Kouhara, Haruhiko; Koga, Masafumi; Saitoh, Youichi; Ohnishi, Takanori; Arita, Norio

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Increased risk for endocrine autoimmunity in Italian type 2 diabetic patients with GAD65 autoantibodies
pp. 565-573(9)
Authors: Gambelunghe, Giovanni; Forini, Francesca; Laureti, Stefano; Murdolo, Giuseppe; Toraldo, Gianluca; Santeusanio, Fausto; Brunetti, Paolo; Sanjeevi, Carani B.; Falorni, Alberto

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Vitamin D receptor gene polymorphisms influence susceptibility to type 1 diabetes mellitus in the Taiwanese population
pp. 575-580(6)
Authors: Chang, Tien-Jyun; Lei, Hsien-Hsien; Yeh, Jih-I; Chiu, Ken C.; Lee, Kuan-Ching; Chen, Mei-Chu; Tai, Tong-Yuan; Chuang, Lee-Ming

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Oestrogen-receptor-α gene polymorphism affects response in bone mineral density to oestrogen in post-menopausal women
pp. 581-585(5)
Authors: Ongphiphadhanakul; Chanprasertyothin; Payatikul; Tung, S. Sae; Piaseu; Chailurkit; Chansirikarn; Puavilai; Rajatanavin

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Spironolactone as a single agent for long-term therapy of hirsute patients
pp. 587-594(8)
Authors: Spritzer, Poli Mara; Lisboa, Karen O.; Mattiello, Simone; Lhullier, Francisco

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Cardiovascular disease in women with polycystic ovary syndrome at long-term follow-up: a retrospective cohort study
pp. 595-600(6)
Authors: Wild, Sarah; Pierpoint, Tracey; McKeigue, Paul; Jacobs, Howard

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Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
pp. 601-607(7)
Authors: Bachega, Tânia A. S. S.; Billerbeck, Ana E. C.; Marcondes, José A. M.; Madureira, Guiomar; Arnhold, Ivo J. P.; Mendonca, Berenice B.

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Growth hormone and prolactin are secreted more irregularly in patients with Cushing's disease
pp. 625-632(8)
Authors: Veldman, Ronald Groote; Frölich, Marijke; Pincus, Steve M.; Veldhuis, Johannes D.; Roelfsema, Ferdinand

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Assessment of disease activity in Graves' ophthalmopathy by orbital ultrasonography and clinical parameters
pp. 641-646(6)
Authors: Gerding, Martin N.; Prummel, Mark F.; Wiersinga, Wilmar M.

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Soluble interleukin-1 receptor antagonist concentration in patients with Graves' ophthalmopathy is neither related to cigarette smoking nor predictive of subsequent response to glucocorticoids
pp. 647-651(5)
Authors: Bartalena, Luigi; Manetti, Luca; Tanda, Maria Laura; Dell'unto, Enrica; Mazzi, Barbara; Rocchi, Roberto; Barbesino, Giuseppe; Pinchera, Aldo; Marcocci, Claudio

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Embolization in combination with radioiodine therapy for bone metastases from differentiated thyroid carcinoma
pp. 653-659(7)
Authors: van Tol, K. M.; Hew, J. M.; Jager, P. L.; Vermey, A.; Dullaart, R. P. F.; Links, T. P.

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Combined pituitary hormone deficiency and pituitary hypoplasia due to a mutation of the Pit-1 gene
pp. 661-665(5)
Authors: Frisch, Herwig; Kim, Christiane; Häusler, Gabriele; Pfäffle, Roland

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Combined pituitary hormone deficiency and pituitary hypoplasia due to a mutation of the Pit-1 gene
pp. 661-665(5)
Authors: Frisch, Herwig; Kim, Christiane; Häusler, Gabriele; Pfäffle, Roland

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