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Endocrinology
- Ruptured functioning adrenal tumour, atypical presentation with renal colic and hypertensionAmr Elmoheen, Mohamed Yousry, Ahmed Elmesery, Khalid BashirBMJ Case Reports CP Dec 2020, 13 (12) e236050; DOI: 10.1136/bcr-2020-236050
- Treatment-induced diabetes neuropathy: description of singular clinical signs to reach a prompt diagnosisPablo Guisado Vasco, Marcos Llanero-Luque, Marta Cano-Megías, María Cortés-BerdoncesBMJ Case Reports CP Dec 2020, 13 (12) e235165; DOI: 10.1136/bcr-2020-235165
- Myasthenia gravis presenting as bilateral pseudointernuclear ophthalmoplegia in a patient with an incidental prolactinomaJulian Fernando Arias Chavez, Cornelius James FernandezBMJ Case Reports CP Dec 2020, 13 (12) e234322; DOI: 10.1136/bcr-2020-234322
- Oncogenic osteomalacia due to phosphaturic mesenchymal tumour in the upper thoracic spineBhavuk Garg, Nishank Mehta, Archit Goyal, Rajesh KhadgawatBMJ Case Reports CP Dec 2020, 13 (12) e238209; DOI: 10.1136/bcr-2020-238209
- Malignant prolongation of the QTc interval due to severe vitamin D deficiency: an unusual presentationPreeti Gupta, Sourabh Agstam, Ashutosh Yadav, Soumitra GhoshBMJ Case Reports CP Dec 2020, 13 (12) e237157; DOI: 10.1136/bcr-2020-237157
- Comprehensive evaluation of bone health using DXA and pQCT in an Indian boy with osteogenesis imperfectaMadhura Bharat Karguppikar, Veena Ekbote, Anuradha Khadilkar, Vaman KhadilkarBMJ Case Reports CP Dec 2020, 13 (12) e236169; DOI: 10.1136/bcr-2020-236169
- Hyperandrogenism caused by ovarian Leydig cell tumour: finding the needle in a haystackChin Voon Tong, Yong Ting TaiBMJ Case Reports CP Dec 2020, 13 (12) e238012; DOI: 10.1136/bcr-2020-238012
- A Patient with speechlessness and rhabdomyolysis: a rare presentation of severe hypocalcaemiaFlorine Helene Jiwa, Kim van den Hoek, Clementine Jaantje Joanna van Zeijl, Albertus Jozef KooterBMJ Case Reports CP Dec 2020, 13 (12) e238072; DOI: 10.1136/bcr-2020-238072
- Diabetic thoracic radiculopathy: a case of a young woman with clinical improvement following immunotherapyAlfonsa C Taiello, Vincenzo La Bella, Rossella SpataroBMJ Case Reports CP Dec 2020, 13 (12) e236412; DOI: 10.1136/bcr-2020-236412
- Adult male patient with severe intellectual disability caused by a homozygous mutation in the HNMT geneWillem M A Verhoeven, Jos I M Egger, Paddy K C Janssen, Arie van HaeringenBMJ Case Reports CP Dec 2020, 13 (12) e235972; DOI: 10.1136/bcr-2020-235972
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