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Publisher: Wiley-Blackwell

Volume 76, Number 1, 1 January 2012

Clinical Endocrinology in 2012: recent changes and future opportunities
pp. 1-1(1)
Authors: Bevan, John; Judd, Stephen; Ball, Steve; Casanueva, Felipe

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Leptin, adiponectin and other adipokines in gestational diabetes mellitus and pre‐eclampsia
pp. 2-11(10)
Authors: Miehle, Konstanze; Stepan, Holger; Fasshauer, Mathias

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Subclinical Cushing’s syndrome: definition and management
pp. 12-18(7)
Authors: Terzolo, M.; Pia, A.; Reimondo, G.

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Metabolic syndrome: is the preadipocyte to blame?*
pp. 19-20(2)
Authors: Lansdown, Andrew; Ludgate, Marian; Rees, Aled

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Identification of the first germline HRPT2 whole‐gene deletion in a patient with primary hyperparathyroidism
pp. 33-38(6)
Authors: Domingues, Rita; Tomaz, Rute Alexandra; Martins, Carmo; Nunes, Carla; Bugalho, Maria João; Cavaco, Branca Maria

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Unacylated ghrelin is associated with changes in insulin sensitivity and lipid profile during an exercise intervention
pp. 39-45(7)
Authors: Cederberg, Henna; Koivisto, Vesa‐Matti; Jokelainen, Jari; Surcel, Heljä‐Marja; Keinänen‐Kiukaanniemi, Sirkka; Rajala, Ulla

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Hyperinsulinemia acutely increases serum macrophage inhibitory cytokine‐1 concentration in anorexia nervosa and obesity
pp. 46-50(5)
Authors: Karczewska‐Kupczewska, Monika; Kowalska, Irina; Nikolajuk, Agnieszka; Adamska, Agnieszka; Otziomek, Elzbieta; Gorska, Maria; Straczkowski, Marek

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Coronary artery disease is associated with higher epicardial Retinol‐binding protein 4 (RBP4) and lower glucose transporter (GLUT) 4 levels in epicardial and subcutaneous adipose tissue
pp. 51-58(8)
Authors: Salgado‐Somoza, Antonio; Teijeira‐Fernández, Elvis; Rubio, José; Couso, Elena; González‐Juanatey, José R.; Eiras, Sonia

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The relationship between fat depot‐specific preadipocyte differentiation and metabolic syndrome in obese women
pp. 59-66(8)
Authors: Park, Hyun Tae; Lee, Eun Sil; Cheon, Yong‐Pil; Lee, Dong Ryul; Yang, Kyung‐Sook; Kim, Young Tae; Hur, Jun Young; Kim, Sun Haeng; Lee, Kyu Wan; Kim, Tak

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Increased prevalence of impaired fasting glucose in MEN1 gene mutation carriers
pp. 67-71(5)
Authors: van Wijk, J. P. H.; Dreijerink, K. M. A.; Pieterman, C. R. C.; Lips, C. J. M.; Zelissen, P. M. J.; Valk, G. D.

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Multiple forms of hypogonadism of central, peripheral or combined origin in males with Prader–Willi syndrome
pp. 72-77(6)
Authors: Radicioni, A. F.; Di Giorgio, G.; Grugni, G.; Cuttini, M.; Losacco, V.; Anzuini, A.; Spera, S.; Marzano, C.; Lenzi, A.; Cappa, M.; Crinò, A.

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Identification of a novel mutation in the exon 2 splice donor site of the POU1F1/PIT‐1 gene in Japanese identical twins with mild combined pituitary hormone deficiency
pp. 78-87(10)
Authors: Inoue, Hiroshi; Mukai, Tokuo; Sakamoto, Yukiko; Kimura, Chizuko; Kangawa, Natsumi; Itakura, Mitsuo; Ogata, Tsutomu; Ito, Yoshiya; Fujieda, Kenji; on behalf of the Japan Growth Genome Consortiumcr10

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Adenoma granulation pattern correlates with clinical variables and effect of somatostatin analogue treatment in a large series of patients with acromegaly
pp. 96-102(7)
Authors: Fougner, Stine Lyngvi; Casar‐Borota, Olivera; Heck, Ansgar; Berg, Jens Petter; Bollerslev, Jens

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The impact of the site of origin and rate of tumour growth on clinical outcome in children with craniopharyngiomas
pp. 103-110(8)
Authors: Qi, Songtao; Pan, Jun; Lu, Yuntao; Gao, Fang; Cao, Ying; Peng, Junxiang; Zhang, Xi’an

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Sex hormone–binding globulin at the crossroad of body composition, somatotropic axis and insulin/glucose homeostasis in young healthy men
pp. 111-118(8)
Authors: Vanbillemont, Griet; Lapauw, Bruno; De Naeyer, Hélène; Roef, Greet; Kaufman, Jean‐Marc; Taes, Youri E. C.

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Shear wave elastography in the diagnosis of thyroid nodules: feasibility in the case of coexistent chronic autoimmune Hashimoto’s thyroiditis
pp. 137-141(5)
Authors: Magri, Flavia; Chytiris, Spyridon; Capelli, Valentina; Alessi, Sarah; Nalon, Elisa; Rotondi, Mario; Cassibba, Sara; Calliada, Fabrizio; Chiovato, Luca

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Decreased serum vascular endothelial growth factor‐D levels in metastatic patients with differentiated thyroid carcinoma
pp. 142-146(5)
Authors: Nersita, Roberto; Matrone, Antonio; Klain, Michele; Scavuzzo, Francesco; Vitolo, Gabriella; Abbondanza, Ciro; Carlino, Maria V.; Giacco, Veronica; Amato, Giovanni; Carella, Carlo

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Assessing the emerging oncogene protein kinase C epsilon as a candidate gene in families with Carney complex‐2
pp. 147-148(2)
Authors: Toledo, Rodrigo A.; Sekiya, Tomoko; Horvath, Anelia; Faucz, Fabio; Fragoso, Maria C. B. V.; Longuini, Viviane C.; Lourenço Jr, Delmar M.; Toledo, Sergio P. A.; Stratakis, Constantine A.

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Molecular analysis of the PAX8 gene in a sample of Mexican patients with primary congenital hypothyroidism: identification of the recurrent p.Arg31His mutation
pp. 148-150(3)
Authors: Alcántara‐Ortigoza, Miguel Angel; González‐del Angel, Ariadna; Martínez‐Cruz, Víctor; Vela‐Amieva, Marcela; Sánchez‐Pérez, Carmen; Moreno‐Rojas, Rosario; Estandía‐Ortega, Bernardette; Hernández‐Martínez, Nancy

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