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Publisher: Wiley-Blackwell

Volume 76, Number 5, 1 May 2012

What is active acromegaly and which parameters do we have?
pp. 609-614(6)
Authors: Neggers, S. J. C. M. M.; Biermasz, N. R.; Lely, A. J.

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Metabolite profiling as a future tool in the prediction of type 2 diabetes mellitus*
pp. 615-616(2)
Authors: Karakas, Mahir; Koenig, Wolfgang

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Predicting the onset of Addison’s disease: ACTH, renin, cortisol and 21‐hydroxylase autoantibodies
pp. 617-624(8)
Authors: Baker, Peter R.; Nanduri, Priyaanka; Gottlieb, Peter A.; Yu, Liping; Klingensmith, Georgeanna J.; Eisenbarth, George S.; Barker, Jennifer M.

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Identification and characterization of C106R, a novel mutation in the DNA‐binding domain of GCMB, in a family with autosomal‐dominant hypoparathyroidism
pp. 625-633(9)
Authors: Yi, Hyon‐Seung; Eom, Young Sil; Park, Ie Byung; Lee, Sangho; Hong, Suntaek; Jüppner, Harald; Mannstadt, Michael; Lee, Sihoon

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Bone turnover markers predict changes in bone mineral density after parathyroidectomy in patients with renal hyperparathyroidism
pp. 634-642(9)
Authors: Lu, Kuo‐Cheng; Ma, Wen‐Ya; Yu, Jyh‐Cherng; Wu, Chia‐Chao; Chu, Pauling

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Stable bone mineral density over 6 years in HIV‐infected men treated with highly active antiretroviral therapy (HAART)
pp. 643-648(6)
Authors: Bolland, Mark J; Grey, Andrew; Horne, Anne M; Briggs, Simon E; Thomas, Mark G; Ellis‐Pegler, Rod B; Gamble, Greg D; Reid, Ian R

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Coagulation and fibrinolytic disturbances are related to carotid intima thickness and arterial blood pressure in Turner syndrome
pp. 649-656(8)
Authors: Gravholt, Claus H.; Mortensen, Kristian H.; Andersen, Niels H.; Ibsen, Liselotte; Ingerslev, Jørgen; Hjerrild, Britta E.

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Urinary mRNA markers of epithelial–mesenchymal transition correlate with progression of diabetic nephropathy
pp. 657-664(8)
Authors: Zheng, Min; Lv, Lin‐Li; Cao, Yu‐Han; Zhang, Jian‐Dong; Wu, Min; Ma, Kun‐Ling; Phillips, Aled O.; Liu, Bi‐Cheng

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The association of specific metabolites of lipid metabolism with markers of oxidative stress, inflammation and arterial stiffness in men with newly diagnosed type 2 diabetes
pp. 674-682(9)
Authors: Ha, Chang Young; Kim, Ji Young; Paik, Jean Kyung; Kim, Oh Yoen; Paik, Yong‐Han; Lee, Eun Jig; Lee, Jong Ho

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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 deficiency
pp. 683-690(8)
Authors: Miletta, Maria Consolata; Scheidegger, Ursina A.; Giordano, Mara; Bozzola, Mauro; Pagani, Sara; Bona, Gianni; Dattani, Mehul; Hindmarsh, Peter C.; Petkovic, Vibor; Oser‐Meier, Monika; Flück, Christa E.; Mullis, Primus‐E.

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Clinical relevance of RET variants G691S, L769L, S836S and S904S to sporadic medullary thyroid cancer
pp. 691-697(7)
Authors: Machens, Andreas; Frank‐Raue, Karin; Lorenz, Kerstin; Rondot, Susanne; Raue, Friedhelm; Dralle, Henning

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Gonadotrophin secretion pattern in anorchid boys from birth to pubertal age: pathophysiological aspects and diagnostic usefulness
pp. 698-705(8)
Authors: Grinspon, Romina P.; Ropelato, María G.; Bedecarrás, Patricia; Loreti, Nazareth; Ballerini, María G.; Gottlieb, Silvia; Campo, Stella M.; Rey, Rodolfo A.

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Growth hormone insensitivity syndrome caused by a heterozygous GHR mutation: phenotypic variability owing to moderation by nonsense‐mediated decay
pp. 706-712(7)
Authors: del Blanco, Darya Gorbenko; de Graaff, Laura C. G.; Visser, Theo J.; Hokken‐Koelega, Anita C. S.

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Birth weight is inversely associated with blood pressure and serum aldosterone and cortisol levels in children
pp. 713-718(6)
Authors: Martinez‐Aguayo, Alejandro; Aglony, Marlene; Bancalari, Rodrigo; Avalos, Carolina; Bolte, Lillian; Garcia, Hernan; Loureiro, Carolina; Carvajal, Cristian; Campino, Carmen; Inostroza, Andrea; Fardella, Carlos

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Novel mutations in MEN1, CDKN1B and AIP genes in patients with multiple endocrine neoplasia type 1 syndrome in Spain
pp. 719-724(6)
Authors: Belar, Oihana; Hoz, Carmen De La; Pérez‐Nanclares, Gustavo; Castaño, Luis; Gaztambide, Sonia; Spanish MEN1 Groupcr6

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Anterior hypopituitarism is rare and autoimmune disease is common in adults with idiopathic central diabetes insipidus
pp. 725-728(4)
Authors: Hannon, M. J.; Orr, C.; Moran, C.; Behan, L. A.; Agha, A.; Ball, S. G.; Thompson, C. J.

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Higher free thyroxine levels are associated with frailty in older men: the Health In Men Study
pp. 741-748(8)
Authors: Yeap, Bu B.; Alfonso, Helman; Paul Chubb, Stephen A.; Walsh, John P.; Hankey, Graeme J.; Almeida, Osvaldo P.; Flicker, Leon

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Coexistent findings of renal glomerular disease with Hashimoto’s thyroiditis
pp. 759-762(4)
Authors: Koçak, Gülay; Huddam, Bülent; Azak, Alper; Ortabozkoyun, Levent; Duranay, Murat

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A phaeochromocytoma occurring in a patient with Parkinson’s disease on l‐dopa therapy: a diagnostic challenge
pp. 763-764(2)
Authors: Collier, Andrew; Ghosh, Sujoy; Breckenridge, Andrew; Perry, Colin G.; Freel, Ellen Marie; Davidson, D. Fraser

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The half‐lives of plasma free metanephrines
pp. 764-766(3)
Authors: Campbell, Kirsten A.; Joseph, Shantha P.; Whiting, Malcolm J.; Doogue, Matthew P.

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Functional studies of CYP21A2 mutants complement structural and clinical predictions of disease severity in CAH
pp. 766-768(3)
Authors: Barbaro, Michela; Soardi, Fernanda C.; Palandi de Mello, Maricilda; Wedell, Anna; Lajic, Svetlana

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