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Publisher: Wiley-Blackwell

Volume 59, Number 2, August 2003

Recent concerns surrounding HRT
pp. 145-155(11)
Authors: Armitage, Mary; Nooney, Janet; Evans, Stephen

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Frequent association between MEN 2A and cutaneous lichen amyloidosis
pp. 156-161(6)
Authors: Verga, Uberta; Fugazzola, Laura; Cambiaghi, Stefano; Pritelli, Chiara; Alessi, Elvio; Cortelazzi, Donatella; Gangi, Emanuela; Beck-Peccoz, Paolo

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Musculoskeletal manifestations in patients with thyroid disease
pp. 162-167(6)
Authors: Cakir, Mehtap; Samanci, Nehir; Balci, Nilufer; Balci, Mustafa Kemal

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The effect of pegvisomant-induced serum IGF-I normalization on serum leptin levels in patients with acromegaly
pp. 168-174(7)
Authors: Parkinson, C.; Whatmore, A. J.; Yates, A. P.; Drake, W. M.; Brabant, G.; Clayton, P. E.; Trainer, P. J.

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Variants in the aromatase gene and on the Y-chromosome are not associated with adult height or insulin resistance in a UK population
pp. 175-179(5)
Authors: Weedon, Michael N.; Turner, Martina; Knight, Beatrice; Clark, Penny; Hattersley, Andrew T.; Frayling, Timothy M.

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Mutational analyses of RB and BRCA2 as candidate tumour suppressor genes in parathyroid carcinoma
pp. 180-189(10)
Authors: Shattuck, Trisha M.; Kim, Teresa S.; Costa, Jessica; Yandell, David W.; Imanishi, Yasuo; Palanisamy, Nallasivam; Gaz, Randall D.; Shoback, Dolores; Clark, Orlo H.; Monchik, John M.; Wierman, Margaret E.; Hollenberg, Anthony; Tojo, Katsuyoshi; Chaganti, R. S. K.; Arnold, Andrew

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Thyroglobulin epitope recognition in a post iodine-supplemented Sri Lankan population
pp. 190-197(8)
Authors: Okosieme, O. E.; Premawardhana, L. D. K. E.; Jayasinghe, A.; de Silva, D. G. H.; Smyth, P. P. A.; Parkes, A. B.; Lejeune, P. J.; Ruf, J.; Lazarus, J. H.

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Partial iodide organification defect caused by a novel mutation of the thyroid peroxidase gene in three siblings
pp. 198-206(9)
Authors: Kotani, Tomio; Umeki, Kazumi; Kawano, Jun–ichi; Suganuma, Tatsuo; Hishinuma, Akira; Ieiri, Tamio; Harada, Shohei

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Detection and localization of chemokine gene expression in autoimmune thyroid disease
pp. 207-213(7)
Authors: Kemp, E. Helen; Metcalfe, Russell A.; Smith, Karen A.; Woodroofe, M. Nicola; Watson, Philip F.; Weetman, Anthony P.

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The pituitary–testicular axis in Klinefelter's syndrome and in oligo-azoospermic patients with and without deletions of the Y chromosome long arm
pp. 214-222(9)
Authors: Tomasi, Paolo A.; Oates, Robert; Brown, Laura; Delitala, Giuseppe; Page, David C.

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Grey-scale analysis allows a quantitative evaluation of thyroid echogenicity in the patients with Hashimoto's thyroiditis
pp. 223-229(7)
Authors: Mazziotti, Gherardo; Sorvillo, Francesca; Iorio, Sergio; Carbone, Antonella; Romeo, Antonio; Piscopo, Marco; Capuano, Salvatore; Capuano, Ermanno; Amato, Giovanni; Carella, Carlo

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Recombinant human TSH testing is a valuable tool for differential diagnosis of congenital hypothyroidism duringl-thyroxine replacement
pp. 230-236(7)
Authors: Fugazzola, Laura; Persani, Luca; Mannavola, Deborah; Reschini, Eugenio; Vannucchi, Guia; Weber, Giovanna; Beck-Peccoz, Paolo

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The N363S polymorphism in the glucocorticoid receptor gene is associated with overweight in subjects with type 2 diabetes mellitus
pp. 237-241(5)
Authors: Roussel, Ronan; Reis, André F.; Dubois-Laforgue, Danièle; Bellanné-Chantelot, Christine; Timsit, José; Velho, Gilberto

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Increased Interleukin-6 levels in pituitary-deficient patients are independently related to their carotid intima-media thickness
pp. 242-250(9)
Authors: Leonsson, M.; Hulthe, J.; Johannsson, G.; Wiklund, O.; Wikstrand, J.; Bengtsson, B. Å.; Oscarsson, J.

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The effectiveness of arginine + GHRH test compared with GHRH + GHRP-6 test in diagnosing growth hormone deficiency in adults
pp. 251-257(7)
Authors: Popovic, Vera; Pekic, Sandra; Doknic, Mirjana; Micic, Dragan; Damjanovic, Svetozar; Zarkovic, Milos; Aimaretti, Gianluca; Corneli, Ginerva; Ghigo, Ezio; Deiguez, Carlos; Casanueva, Felipe F.

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The effect of body weight and weight loss on thyroid volume and function in obese women
pp. 258-262(5)
Authors: Sari, Ramazan; Balci, Mustafa Kemal; Altunbas, Hasan; Karayalcin, Umit

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Novel missense mutation (Arg432Cys) in a patient with steroid sulphatase-deficiency
pp. 263-264(2)
Authors: González-Huerta, L. M.; Riviera-Vega, M. R.; Kofman-Alfeuro, S. H.; Cuevas-Covarrubias, S. A.

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Psychological well-being of patients onl-thyroxine
pp. 264-265(2)
Authors: Edwards, C. M. B.; Cox, J. P. D.; Robinson, S.

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