Clinical Endocrinology

Primary ovarian insufficiency: a more accurate term for premature ovarian failure
pp. 499-509(11)
Author: Welt, Corrine K.

The association between the renin-angiotensin-aldosterone system and arterial stiffness in young healthy subjects
pp. 510-512(3)
Authors: Shapiro, Y.; Boaz, M.; Matas, Z.; Fux, A.; Shargorodsky, M.

Bilateral laparoscopic adrenalectomy for corticotrophin-dependent Cushing's syndrome: a review of the Mayo Clinic experience
pp. 513-519(7)
Authors: Chow, John T.; Thompson, Geoffrey B.; Grant, Clive S.; Farley, David R.; Richards, Melanie L.; Young, William F.

The management of high-risk patients with primary hyperparathyroidism - minimally invasive parathyroidectomy vs. medical treatment
pp. 520-528(9)
Authors: Fang, Wen-Liang; Tseng, Ling-Ming; Chen, Jui-Yu; Chiou, See-Ying; Chou, Yi-Hong; Wu, Chew-Wun; Lee, Chen-Hsen

Novel melanocortin 4 receptor gene mutations in severely obese children
pp. 529-535(7)
Authors: Lee, Yung Seng; Poh, Larry Kok Seng; Kek, Betty Lay Kee; Loke, Kah Yin

Short-term treatment with ezetimibe, simvastatin or their combination does not alter circulating adiponectin, resistin or leptin levels in healthy men
pp. 536-541(6)
Authors: Gouni-Berthold, Ioanna; Berthold, Heiner K.; Chamberland, John P.; Krone, Wilhelm; Mantzoros, Christos S.

Endothelial nitric oxide synthase Glu298Asp, 4b/a, and T-786C polymorphisms in type 2 diabetic retinopathy
pp. 542-546(5)
Authors: Ezzidi, Intissar; Mtiraoui, Nabil; Mohamed, Manel Ben Hadj; Mahjoub, Touhami; Kacem, Maha; Almawi, Wassim Y.

Leptin therapy for partial lipodystrophy linked to a PPAR-γ mutation
pp. 547-554(8)
Authors: Guettier, Jean-Marc; Park, Jean Y.; Cochran, Elaine K.; Poitou, Christine; Basdevant, Arnaud; Meier, Muriel; Clément, Karine; Magré, Jocelyne; Gorden, Phillip

Serum retinol-binding protein 4 levels are elevated in non-alcoholic fatty liver disease
pp. 555-560(6)
Authors: Seo, J. A.; Kim, N. H.; Park, S. Y.; Kim, H. Y.; Ryu, O. H.; Lee, K. W.; Lee, J.; Kim, D. L.; Choi, K. M.; Baik, S. H.; Choi, D. S.; Kim, S. G.

Mutations associated with succinate dehydrogenased-related malignant paragangliomas
pp. 561-566(6)
Authors: Timmers, Henri J. L. M.; Pacak, Karel; Bertherat, Jérôme; Lenders, Jacques W. M.; Duet, Michèle; Eisenhofer, Graeme; Stratakis, Constantine A.; Niccoli-Sire, Patricia; Huy, Patrice Tran Ba; Burnichon, Nelly; Gimenez-Roqueplo, Anne-Paule

Homozygosity of the d3-growth hormone receptor polymorphism is associated with a high total effect of GH on growth and a low BMI in girls with Turner syndrome
pp. 567-572(6)
Authors: Binder, Gerhard; Trebar, Branko; Baur, Friederike; Schweizer, Roland; Ranke, Michael B.

Three years prospective investigation of anterior pituitary function after traumatic brain injury: a pilot study
pp. 573-579(7)
Authors: Tanriverdi, Fatih; Ulutabanca, Halil; Unluhizarci, Kursad; Selcuklu, Ahmet; Casanueva, Felipe F.; Kelestimur, Fahrettin

Detailed functional studies on androgen receptor mild mutations demonstrate their association with male infertility
pp. 580-588(9)
Authors: Zuccarello, D.; Ferlin, A.; Vinanzi, C.; Prana, E.; Garolla, A.; Callewaert, L.; Claessens, F.; Brinkmann, A. O.; Foresta, C.

Bioavailable testosterone is associated with a reduced risk of amnestic mild cognitive impairment in older men
pp. 589-598(10)
Authors: Chu, Leung-Wing; Tam, Sidney; Lee, Peter W. H.; Wong, Rachel L. C.; Yik, Ping-Yiu; Tsui, Wilson; Song, Youqiang; Cheung, Bernard M. Y.; Morley, John E.; Lam, Karen S. L.

Is the management of thyroid nodules and differentiated thyroid cancer in accordance with recent consensus guidelines? - Results of a national survey
pp. 599-604(6)
Authors: Van den Bruel, A.; Moreno-Reyes, R.; Bex, M.; Daumerie, C.; Glinoer, D.

Radioiodine therapy after pretreatment with bexarotene for metastases of differentiated thyroid carcinoma
pp. 605-609(5)
Authors: Liu, Ying Y.; Stokkel, Marcel P.; Morreau, Hans A.; Pereira, Alberto M.; Romijn, Johannes A.; Smit, Johannes W. A.

A systematic review of the gonadal effects of therapeutic radioactive iodine in male thyroid cancer survivors
pp. 610-617(8)
Authors: Sawka, Anna M.; Lea, Jane; Alshehri, Bandar; Straus, Sharon; Tsang, Richard W.; Brierley, James D.; Thabane, Lehana; Rotstein, Lorne; Gafni, Amiram; Ezzat, Shereen; Goldstein, David P.

BRAF mutation associated with other genetic events identifies a subset of aggressive papillary thyroid carcinoma
pp. 618-634(17)
Authors: Costa, Angela M.; Herrero, Agustín; Fresno, Manuel F.; Heymann, Jonas; Alvarez, José Antonio; Cameselle-Teijeiro, Jose; García-Rostán, Ginesa

The impact of thyroid eye disease upon patients' wellbeing: a qualitative analysis
pp. 635-639(5)
Authors: Estcourt, Stephanie; Vaidya, Bijay; Quinn, Anthony; Shepherd, Maggie

Chronic unexplained anaemia in isolated autoimmune thyroid disease or associated with autoimmune related disorders
pp. 640-645(6)
Authors: Sibilla, Rosanna; Santaguida, Maria Giulia; Virili, Camilla; Gargano, Lucilla; Nardo, Serena; Guardia, Michele Della; Viceconti, Nicola; Franchi, Antonella; Centanni, Marco

Association of genetic variants in GABRA3 gene and thyrotoxic hypokalaemic periodic paralysis in Thai population
pp. 646-651(6)
Authors: Jongjaroenprasert, Wallaya; Chanprasertyotin, Suwannee; Butadej, Siriwan; Nakasatien, Soontaree; Charatcharoenwitthaya, Natthinee; Himathongkam, Thep; Ongphiphadhanakul, Boonsong

Heritability of serum TSH, free T4 and free T3 concentrations: a study of a large UK twin cohort
pp. 652-659(8)
Authors: Panicker, V.; Wilson, S. G.; Spector, T. D.; Brown, S. J.; Falchi, M.; Richards, J. B.; Surdulescu, G. L.; Lim, E. M.; Fletcher, S. J.; Walsh, J. P.

Relation between plasma fibroblast growth factor-23, serum fetuin-A levels and coronary artery calcification evaluated by multislice computed tomography in patients with normal kidney function
pp. 660-665(6)
Authors: Roos, Marcel; Lutz, Jens; Salmhofer, Hermann; Luppa, Peter; Knauß, Amelie; Braun, Siegmund; Martinof, Stefan; Schömig, Albert; Heemann, Uwe; Kastrati, Adnan; Hausleiter, Jörg

MEN2 screening dilemmas in a family with a novel RET mutation in the MEN2 susceptibility region of the gene, a family history of Hirschsprung disease, and no family history of MEN2-related tumours
pp. 666-667(2)
Authors: Clowes, Virginia E.; Shaw-Smith, Charles; Simpson, Helen; Ball, Steve G.; Acerini, Carlo L.

Adrenal crisis causing critical illness related reversible myocardial dysfunction
pp. 667-669(3)
Authors: Sherlock, Mark; Gittoes, Neil J.; Arlt, Wiebke

Resolution of secondary amenorrhoea following withdrawal of dihydocodeine
pp. 669-670(2)
Authors: Gonzalez, Susana; Murray, Robert D.