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Jes Sloth Mathiesen, Jens Peter Kroustrup, Peter Vestergaard, Kirstine Stochholm, Per Løgstrup Poulsen, Åse Krogh Rasmussen, Ulla Feldt-Rasmussen, Sten Schytte, Stefano Christian Londero, Henrik Baymler Pedersen, Christoffer Holst Hahn, Bjarki Ditlev Djurhuus, Jens Bentzen, Sören Möller, Mette Gaustadnes, Maria Rossing, Finn Cilius Nielsen, Kim Brixen, Anja Lisbeth Frederiksen, Christian Godballe and the Danish Thyroid Cancer Group (DATHYRCA)

. Additionally, we describe prevalence changes over time. Patients and methods Patients This retrospective cohort study included 474 unique patients diagnosed with MTC in Denmark between January 1, 1960 and December 31, 2014. Of these, 356 were

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Marloes Emous, Merel van den Broek, Ragnhild B Wijma, Loek J M de Heide, Gertjan van Dijk, Anke Laskewitz, Erik Totté, Bruce H R Wolffenbuttel and André P van Beek

, which may even result in coma ( 4 , 5 , 6 ). Studies have observed prevalence rates after primary gastric bypass surgery of 12% when assessed by means of questionnaires and up to 75% when assessed by continuous glucose monitoring systems (CGMSs) ( 7

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Rasha Odeh, Abeer Alassaf, Lubna Gharaibeh, Sarah Ibrahim, Fareed Khdair Ahmad and Kamel Ajlouni

Introduction Type 1 diabetes mellitus (T1D) is an immune-mediated disease that is known to be associated with other autoimmune conditions, most commonly thyroiditis and celiac disease (CD). While the prevalence of CD in the general population

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Jeonghoon Ha, Jeongmin Lee, Kwanhoon Jo, Dong-Jun Lim, Moo Il Kang, Bong Yun Cha and Min-Hee Kim

cases, thyroid hormone replacement can be considered in pregnant patients who have TSH persistently >10 µIU/mL, associated symptoms or are at high risk of overt hypothyroidism ( 2 , 3 ). SCH is frequently detected in the population with a prevalence of

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Nella Augusta Greggio, Elisa Rossi, Silvia Calabria, Alice Meneghin, Joaquin Gutierrez de Rubalcava, Carlo Piccinni and Antonella Pedrini

diagnostic testing is still open. The prevalence of thyroid dysfunctions among general population ranges from 1 to 10%, with higher estimates among women (up to 8 times rather than men) and elderly ( 1 , 2 ). The National Health and Nutrition Examination

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Chunyun Fu, Shiyu Luo, Yingfeng Li, Qifei Li, Xuehua Hu, Mengting Li, Yue Zhang, Jiasun Su, Xuyun Hu, Yun Chen, Jin Wang, Bobo Xie, Jingsi Luo, Xin Fan, Shaoke Chen and Yiping Shen

reported a CH prevalence of 1:666 (TSH cutoff level 10 IU/L) in East Azerbaijan, Iran ( 4 ), whereas a CH prevalence of 1:2591 (TSH cutoff level 10 IU/L) was reported in the Republic of Macedonia ( 5 ). Two previous studies reported the CH prevalence based

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A V Dreval, I V Trigolosova, I V Misnikova, Y A Kovalyova, R S Tishenina, I A Barsukov, A V Vinogradova and B H R Wolffenbuttel

early carbohydrate metabolism disorders (ECMDs) – defined as IFG, IGT or their combination – its prevalence in patients with acromegaly has been shown to vary between 16 and 46% (3, 4, 5) . While most epidemiological studies have shown the prevalence of

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Volha V Zhukouskaya, Anya Rothenbuhler, Annamaria Colao, Carolina Di Somma, Peter Kamenický, Séverine Trabado, Dominique Prié, Christelle Audrain, Anna Barosi, Christèle Kyheng, Anne-Sophie Lambert and Agnès Linglart

(50.0 ± 1.8 cm (1.3 ± 6.4SDS) vs 49.0 ± 2.3 cm (−0.3 ± 1.2SDS), P  = 0.006, respectively) and tended to have a lower prevalence of SGA compared to those with XLH-family history (3.6% vs 8.7%, P  = 0.3, respectively). Regarding the children with a

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Johan Verhelst, Anders F Mattsson, Cecilia Camacho-Hübner, Anton Luger and Roger Abs

). Patients with AO-GHD have a prevalence of MetS between 1.3- and 2-fold that of the general population ( 1 , 4 ) and this varies depending on the studies between 31.0 and 56.6% ( 1 , 2 , 3 , 4 ). The elevated MetS prevalence in GHD is probably of

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Katerina Saltiki, Elli Anagnostou, George Simeakis, Sofia Kouki, Anastasia Angelopoulou, Leda Sarika, Alexandra Papathoma and Maria Alevizaki

high prevalence in patients with inherited MTC in Greece ( 11 ). Their significant proportion had previously been considered as sporadic, before the routine screening for this specific mutation had been introduced ( 11 , 12 ). A genotype