ISSN 0300-0664 (Print); ISSN 1365-2265 (Online)
Publisher: Wiley-Blackwell
Primary hyperparathyroidism and the skeleton pp. 1-19(19) Author: Mosekilde, Leif
Clinical and biochemical characteristics of normotensive patients with primary aldosteronism: a comparison with hypertensive cases pp. 20-28(9) Authors: Médeau, Virginie; Moreau, François; Trinquart, Ludovic; Clemessy, Maud; Wémeau, Jean-Louis; Vantyghem, Marie Christine; Plouin, Pierre-François; Reznik, Yves
Parathyroid response to vitamin D insufficiency: relations to bone, body composition and to lifestyle characteristics pp. 29-35(7) Authors: Rejnmark, Lars; Vestergaard, Peter; Brot, Christine; Mosekilde, Leif
The G/G genotype of a single nucleotide polymorphism at –1066 of c-Jun N-terminal kinase 1 gene (MAPK8) does not affect type 2 diabetes susceptibility despite the specific binding of AP2α pp. 36-44(9) Authors: Osawa, Haruhiko; Yamada, Kazuya; Tabara, Yasuharu; Ochi, Masaaki; Onuma, Hiroshi; Nishida, Wataru; Shimizu, Ikki; Kawamoto, Ryuichi; Fujii, Yasuhisa; Miki, Tetsuro; Ohashi, Jun; Makino, Hideichi
Variation in Niemann–Pick C1-like 1 gene as a determinant of apolipoprotein B-100 kinetics and response to statin therapy in centrally obese men pp. 45-51(7) Authors: Chan, Dick C.; Watts, Gerald F.; Wang, Jian; Hegele, Robert A.; van Bockxmeer, Frank M.; Barrett, P. Hugh R.
The evaluation of metabolic parameters and insulin sensitivity for a more robust diagnosis of the polycystic ovary syndrome pp. 52-60(9) Authors: Amato, Marco Calogero; Galluzzo, Aldo; Finocchiaro, Sara; Criscimanna, Angela; Giordano, Carla
A novel phenotypic expression associated with a new mutation in LMNA gene, characterized by partial lipodystrophy, insulin resistance, aortic stenosis and hypertrophic cardiomyopathy pp. 61-68(8) Authors: Araújo-Vilar, David; Lado-Abeal, Joaquin; Palos-Paz, Fernando; Lattanzi, Giovanna; Bandín, Manuel A.; Bellido, Diego; Domínguez-Gerpe, Lourdes; Calvo, Carlos; Pérez, Oscar; Ramazanova, Alia; Martínez-Sánchez, Noelia; Victoria, Berta; Costa-Freitas, Ana Teresa
Serum levels of the adipokine visfatin are increased in pre-eclampsia pp. 69-73(5) Authors: Fasshauer, Mathias; Waldeyer, Theresa; Seeger, Jeannette; Schrey, Susanne; Ebert, Thomas; Kratzsch, Jurgen; Lossner, Ulrike; Bluher, Matthias; Stumvoll, Michael; Faber, Renaldo; Stepan, Holger
Serum resistin is positively correlated with the accumulation of metabolic syndrome factors in type 2 diabetes pp. 74-80(7) Authors: Osawa, Haruhiko; Ochi, Masaaki; Tabara, Yasuharu; Kato, Kenichi; Yamauchi, Junko; Takata, Yasunori; Nishida, Wataru; Onuma, Hiroshi; Shimizu, Ikki; Fujii, Yasuhisa; Miki, Tetsuro; Ohashi, Jun; Makino, Hideichi
Familial prevalence and age of RET germline mutations: implications for screening pp. 81-87(7) Authors: Machens, Andreas; Dralle, Henning
Insulin, adiponectin, IGFBP-1 levels and body composition in small for gestational age born non-obese children during prepubertal ages pp. 88-92(5) Authors: Sancakli, Ozlem; Darendeliler, Feyza; Bas, Firdevs; Gokcay, Gulbin; Disci, Rian; Aki, Semih; Eskiyurt, Nurten
Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole pp. 93-98(6) Authors: Almeida, Madson Queiroz; Brito, Vinicius Nahime; Lins, Thereza Selma S.; Guerra-Junior, Gil; de Castro, Margaret; Antonini, Sonir Roberto; Arnhold, Ivo Jorge Prado; Mendonca, Berenice Bilharinho; Latronico, Ana Claudia
Polymorphisms of the ghrelin/obestatin gene and ghrelin levels in Chinese children with short stature pp. 99-104(6) Authors: Zou, Chao Chun; Huang, Ke; Liang, Li; Zhao, Zheng Yan
Gonadotrophic status in adolescents with pituitary stalk interruption syndrome pp. 105-111(7) Authors: Rottembourg, Diane; Linglart, Agnès; Adamsbaum, Catherine; Lahlou, Najiba; Teinturier, Cécile; Bougnères, Pierre; Carel, Jean-Claude
Facial and pituitary morphology are related in Dutch patients with GH deficiency pp. 112-116(5) Authors: de Graaff, L. C. G.; Baan, J.; Govaerts, L. C. P.; Hokken-Koelega, A. C. S.
Role for postoperative cortisol response to desmopressin in predicting the risk for recurrent Cushing's disease pp. 117-122(6) Authors: Romanholi, Daniella Jesus Patrick Carminatti; Machado, Marcio Carlos; Pereira, Camila Canteiro; Danilovic, Debora Seguro; Pereira, Maria Adelaide Albergaria; Cescato, Valter Angelo S.; Neto, Malebranche Berardo C. Cunha; Musolino, Nina Rosa Castro; de Mendonça, Berenice Bilharinho; Salgado, Luiz Roberto
Previous radiotherapy negatively influences quality of life during 4 years of follow-up in patients cured from acromegaly pp. 123-128(6) Authors: van der Klaauw, Agatha A.; Biermasz, Nienke R.; Hoftijzer, Hendrieke C.; Pereira, Alberto M.; Romijn, Johannes A.
Heritability of blood concentrations of sex-steroids in relation to body composition in young adult male siblings pp. 129-135(7) Authors: Bogaert, Veerle; Taes, Youri; Konings, Peter; Van Steen, Kristel; De Bacquer, Dirk; Goemaere, Stefan; Zmierczak, Hans; Crabbe, Patricia; Kaufman, Jean-Marc
Influence of iodine on the reference interval of TSH and the optimal interval of TSH: results of a follow-up study in areas with different iodine intakes pp. 136-141(6) Authors: Guan, Haixia; Shan, Zhongyan; Teng, Xiaochun; Li, Yushu; Teng, Di; Jin, Ying; Yu, Xiaohui; Fan, Chenling; Chong, Wei; Yang, Fan; Dai, Hong; Yu, Yang; Li, Jia; Chen, Yanyan; Zhao, Dong; Shi, Xiaoguang; Hu, Fengnan; Mao, Jinyuan; Gu, Xiaolan; Yang, Rong; Chen, Wei; Tong, Yajie; Wang, Weibo; Gao, Tianshu; Li, Chenyang; Teng, Weiping
A novel therapeutic paradigm to treat congenital hypothyroidism pp. 142-147(6) Authors: Mathai, Sarah; Cutfield, Wayne S.; Gunn, Alistair J.; Webster, Dianne; Jefferies, Craig; Robinson, Elizabeth; Hofman, Paul
Primary cell cultures from anaplastic thyroid cancer obtained by fine-needle aspiration used for chemosensitivity tests pp. 148-152(5) Authors: Antonelli, Alessandro; Ferrari, Silvia Martina; Fallahi, Poupak; Berti, Piero; Materazzi, Gabriele; Barani, Lucio; Marchetti, Ivo; Ferrannini, Ele; Miccoli, Paolo
Sizes of abdominal organs in adults with severe short stature due to severe, untreated, congenital GH deficiency caused by a homozygous mutation in the GHRH receptor gene pp. 153-158(6) Authors: Oliveira, Carla R. P.; Salvatori, Roberto; Nóbrega, Luciana M. A.; Carvalho, Erick O. M.; Menezes, Menilson; Farias, Catarine T.; Britto, Allan V. O.; Pereira, Rossana M. C.; Aguiar-Oliveira, Manuel H.
Assessment of the efficacy and safety of intravenous conivaptan in patients with euvolaemic hyponatraemia: subgroup analysis of a randomized, controlled study pp. 159-168(10) Authors: Verbalis, Joseph G.; Zeltser, David; Smith, Neila; Barve, Abhijit; Andoh, Masakazu
Conventional withdrawal of thyroid hormone before radioiodine therapy in differentiated thyroid carcinoma: how frequently are adequately raised TSH levels attained? pp. 169-170(2) Authors: McLaughlin, C. M.; Hunter, S. J.; Bell, P. M.; McCance, D. R.; Sheridan, B.; Atkinson, A. B.
Complex disease phenotype revealed by GH deficiency associated with a novel and unusual defect in the GH-1 gene pp. 170-172(3) Authors: Iughetti, Lorenzo; Sobrier, Marie-Laure; Predieri, Barbara; Netchine, Irene; Carani, Cesare; Bernasconi, Sergio; Balli, Fiorella; Amselem, Serge
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