Clinical Endocrinology

New treatments in type 2 diabetes: a focus on the incretin-based therapies
pp. 343-353(11)
Author: Barnett, Anthony H.

When should genetic testing be obtained in a patient with phaeochromocytoma or paraganglioma?
pp. 354-357(4)
Authors: Erlic, Zoran; Neumann, Hartmut P. H.

The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease
pp. 358-362(5)
Authors: Roycroft, Matthew; Fichna, Marta; McDonald, David; Owen, Kate; Żurawek, Magdalena; Gryczyńska, Maria; Januszkiewicz-Lewandowska, Danuta; Fichna, Piotr; Cordell, Heather; Donaldson, Peter; Nowak, Jerzy; Pearce, Simon

Effects of genetic variation in the aldosterone synthase (CYP11B2) gene on enzyme function
pp. 363-371(9)
Authors: Holloway, C. D.; MacKenzie, S. M.; Fraser, R.; Miller, S.; Barr, M.; Wilkinson, D.; Forbes, G. H.; Friel, E.; Connell, J. M. C.; Davies, E.

Vitamin D, PTH and calcium levels in pregnant women and their neonates
pp. 372-377(6)
Authors: Bowyer, Lucy; Catling-Paull, Christine; Diamond, Terrence; Homer, Caroline; Davis, Gregory; Craig, Maria E.

Spinal volumetric trabecular bone mass in acromegalic patients: a longitudinal study
pp. 378-382(5)
Authors: Battista, Claudia; Chiodini, Iacopo; Muscarella, Silvana; Guglielmi, Giuseppe; Mascia, Maria Lucia; Carnevale, Vincenzo; Scillitani, Alfredo

Ghrelin and the differential regulation of des-acyl (DSG) and oct-anoyl ghrelin (OTG) in human adipose tissue (AT)
pp. 383-389(7)
Authors: Kos, K.; Harte, A. L.; O'Hare, P. J.; Kumar, S.; McTernan, P. G.

Variant rs9939609 in the FTO gene is associated with obesity in an adult population from Spain
pp. 390-393(4)
Authors: González-Sánchez, José L.; Zabena, Carina; Martínez-Larrad, María T.; Martínez-Calatrava, María J.; Pérez-Barba, Milagros; Serrano-Ríos, Manuel

Inflammatory markers and visceral fat are inversely associated with maximal oxygen consumption in women with polycystic ovary syndrome (PCOS)
pp. 394-400(7)
Authors: Giallauria, Francesco; Palomba, Stefano; De Sio, Ilario; Maresca, Luigi; Vuolo, Laura; Savastano, Silvia; Lombardi, Gaetano; Colao, Annamaria; Vigorito, Carlo; Orio, Francesco

Interleukin-10-592C/A, -819C/T and -1082A/G promoter variants affect the susceptibility to nephropathy in Tunisian type 2 diabetes (T2DM) patients
pp. 401-407(7)
Authors: Ezzidi, Intissar; Mtiraoui, Nabil; Kacem, Maha; Mallat, Samir G.; Mohamed, Manel Ben Hadj; Chaieb, Molka; Mahjoub, Touhami; Almawi, Wassim Y.

Impact of adiponectin and ghrelin on incident glucose intolerance and on weight change
pp. 408-414(7)
Authors: Bennett, Nadia R.; Boyne, Michael S.; Cooper, Richard S.; Royal-Thomas, Tamika Y.; Bennett, Franklyn I.; Luke, Amy; Wilks, Rainford J.; Forrester, Terrence E.

Relationship between clinical features and gastric emptying disturbances in diabetes mellitus
pp. 415-420(6)
Authors: Bharucha, Adil E.; Camilleri, Michael; Forstrom, Lee A.; Zinsmeister, Alan R.

Evaluation of the autoimmune regulator (AIRE) gene mutations in a cohort of Italian patients with autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy (APECED) and in their relatives
pp. 421-428(8)
Authors: Cervato, Sara; Mariniello, Barbara; Lazzarotto, Francesca; Morlin, Luca; Zanchetta, Renato; Radetti, Giorgio; De Luca, Filippo; Valenzise, Mariella; Giordano, Roberta; Rizzo, Daniela; Giordano, Carla; Betterle, Corrado

A pilot study to evaluate gene expression profiles in peripheral blood mononuclear cells (PBMCs) from children with GH deficiency and Turner syndrome in response to GH treatment
pp. 429-434(6)
Authors: Whatmore, Andrew J.; Patel, Leena; Clayton, Peter E.

GH replacement in patients with non-functioning pituitary adenoma (NFA) treated solely by surgery is not associated with increased risk of tumour recurrence
pp. 435-438(4)
Authors: Arnold, J. R.; Arnold, D. F.; Marland, A.; Karavitaki, N.; Wass, J. A. H.

Use of a GH receptor antagonist (GHRA) to explore the relationship between GH and IGF-I in adults with severe GH deficiency (GHD)
pp. 439-445(7)
Authors: Berg, C. A.; Pokrajac, A.; Bidlingmaier, M.; Strasburger, C. J.; Shalet, S. M.; Trainer, P. J.

Prevalence of low male testosterone levels in primary care in Germany: cross-sectional results from the DETECT study
pp. 446-454(9)
Authors: Schneider, Harald Jörn; Sievers, Caroline; Klotsche, Jens; Böhler, Steffen; Pittrow, David; Lehnert, Hendrik; Wittchen, Hans-Ulrich; Stalla, Günter Karl

Healthier lifestyle predicts higher circulating testosterone in older men: the Health In Men Study
pp. 455-463(9)
Authors: Yeap, Bu B.; Almeida, Osvaldo P.; Hyde, Zoë; Norman, Paul E.; Chubb, S. A. Paul; Jamrozik, Konrad; Hankey, Graeme J.; Flicker, Leon

The Pro¹²Ala PPARγ gene polymorphism: possible modifier of the activity and severity of thyroid-associated orbitopathy (TAO)
pp. 464-468(5)
Authors: Alevizaki, Maria; Mantzou, Emily; Cimponeriu, Adriana; Saltiki, Katerina; Philippou, George; Wiersinga, Wilmar

Serum total antioxidant status and lipid peroxidation marker malondialdehyde levels in overt and subclinical hypothyroidism
pp. 469-474(6)
Authors: Torun, Ayse Nur; Kulaksizoglu, Sevsen; Kulaksizoglu, Mustafa; Pamuk, Baris Onder; Isbilen, Elif; Tutuncu, Neslihan Bascil

Down-regulation of NR4A1 in follicular thyroid carcinomas is restored following lithium treatment
pp. 475-483(9)
Authors: Camacho, Cléber P.; Latini, Flavia R. M.; Oler, Gisele; Hojaij, Flavio C.; Maciel, Rui M. B.; Riggins, Gregory J.; Cerutti, Janete M.

Thyroid function and the natural history of depression: findings from the Caerphilly Prospective Study (CaPS) and a meta-analysis
pp. 484-492(9)
Authors: Williams, M. D.; Harris, R.; Dayan, C. M.; Evans, J.; Gallacher, J; Ben-Shlomo, Y.

Health-related quality of life in long-term follow-up of patients with cured TNM Stage I or II differentiated thyroid carcinoma
pp. 493-497(5)
Authors: Pelttari, Hanna; Sintonen, Harri; Schalin-Jäntti, Camilla; Välimäki, Matti J.

Serum tumour necrosis factor-alpha and interleukin-8 levels in acromegalic patients: acromegaly may be associated with moderate inflammation
pp. 498-499(2)
Authors: Arikan, Senay; Bahceci, Mithat; Tuzcu, Alpaslan; Gokalp, Deniz

Germline mutations in the CDKN1B gene encoding p27^Kip1 are a rare cause of multiple endocrine neoplasia type 1
pp. 499-500(2)
Authors: Owens, Martina; Stals, Karen; Ellard, Sian; Vaidya, Bijay

Sexual dimorphism of high molecular weight adiponectin in cord blood
pp. 500-501(2)
Authors: Lau, Sue Mei; Hng, Tien Ming; de Vries, Brad; McLean, Mark; Cheung, N Wah