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G Giuffrida, F Ferraù, R Laudicella, O R Cotta, E Messina, F Granata, F F Angileri, A Vento, A Alibrandi, S Baldari and S Cannavò

effectiveness, safety and long-term outcome of PRRT in three patients (2 F, 1 M) with aggressive giant PT treated by our group, also reviewing the little data available in literature about this therapeutic option. Patients and methods Between 2009 and

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Jan Calissendorff and Henrik Falhammar

University Hospital, Stockholm, Sweden. All patients with an International Classification of Diseases version 10 (ICD-10), with a code of E050 (Graves’ thyrotoxicosis) and treated with iodine during 2005–2015 were included and all medical files were reviewed

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Marieke Stientje Velema, Aline de Nooijer, Ad R M M Hermus, Henri J L M Timmers, Jacques W M Lenders, Olga Husson and Jaap Deinum

Radboud University Medical Center judged that no detailed review was warranted given the non-intrusive and non-experimental character of this study. We obtained written informed consent of all patients. Phase I This phase was aimed at compiling an

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Jordyn Silverstein, Wesley Kidder, Susan Fisher, Thomas A Hope, Samantha Maisel, Dianna Ng, Jessica Van Ziffle, Chloe E Atreya and Katherine Van Loon

-partum period ( 15 , 16 , 17 ). A 1993 study examined 41 cases of pregnant women with metastatic CRC, reporting that the majority of cases (64%) originated in the rectum ( 9 ). A systematic review of 119 case reports of CRC diagnosed during pregnancy, compared

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Changjiao Yan, Meiling Huang, Xin Li, Ting Wang and Rui Ling

. After institutional review board approval and informed patient consenting, we retrospectively collected detailed BRAF V600E and clinicopathologic data from institutional patient records. The epidemiological data and clinicopathological features were

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Marianne C Astor, Kristian Løvås, Anette S B Wolff, Bjørn Nedrebø, Eirik Bratland, Jon Steen-Johnsen and Eystein S Husebye

receptor potential cation channel member 6 ( TRPM6 ), claudin 16 and 19, cyclin M2 ( CNNM2 ) and the EGF . For review, see (4) . Primary hypomagnesemia with secondary hypocalcemia (HSH) is an autosomal recessive disease characterized by reduced intestinal

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Ashley K Clift, Oskar Kornasiewicz, Panagiotis Drymousis, Omar Faiz, Harpreet S Wasan, James M Kinross, Thomas Cecil and Andrea Frilling

.9 years and no significant gender disparity have been reported in a systematic review of 600 patients ( 6 ). Historically often regarded as part of the spectrum of neuroendocrine neoplasms, GCC do indeed display a degree of neuroendocrine differentiation

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Yiqiang Huang, Lin-ang Wang, Qiubo Xie, Jian Pang, Luofu Wang, Yuting Yi, Jun Zhang, Yao Zhang, Rongrong Chen, Weihua Lan, Dianzheng Zhang and Jun Jiang

immunohistochemistry. Materials and methods Patients and genetic testing The Institutional Review Board of Daping Hospital of the Third Military Medical University approved this study. Written informed consents were obtained from the patients for use of

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Monia Cito, Silvia Pellegrini, Lorenzo Piemonti and Valeria Sordi

double over the next decade (for review see ( 2 )). Since 1922, exogenous insulin administration has been the most important lifesaving intervention for all T1D patients; however, chronic insulin treatment is a double-edged sword since it fails to

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Alexis Sudlow, Carel W le Roux and Dimitri J Pournaras

K Banel D Jensen MD Pories WJ Bantle JP Sledge I . Weight and type 2 diabetes after bariatric surgery: systematic review and meta-analysis . American Journal of Medicine 2009 248.e5 – 256.e5 . ( https://doi.org/10.1016/j.amjmed.2008