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Fluid electrolyte and acid-base disturbances
- Hypokalaemic quadriparesis in a patient with urinary diversion through Indiana pouchSrinivasa Anurag Kuchulakanti, Pradeep M ShenoyBMJ Case Reports CP Apr 2022, 15 (4) e248123; DOI: 10.1136/bcr-2021-248123
- Hyperglycinuria: diagnosis in middle ageHithem Fargaly, Shobi Mathew, Noreen F RossiBMJ Case Reports CP Mar 2022, 15 (3) e246252; DOI: 10.1136/bcr-2021-246252
- Use of Venous Excess UltraSound (VExUS) score in hyponatraemia management in critically ill patientRita Varudo, Inês Pimenta, Jacobo Bacariza Blanco, Filipe André GonzalezBMJ Case Reports CP Feb 2022, 15 (2) e246995; DOI: 10.1136/bcr-2021-246995
- Successful living kidney donation from a patient with a Gitelman’s syndromeMilad Darrat, Hannah Likinyo, Shin-Howe Ryan Winata, Sarah Morgan, Aisling E Courtney, John LindsayBMJ Case Reports CP Feb 2022, 15 (2) e246162; DOI: 10.1136/bcr-2021-246162
- Refractory familial hypokalaemic periodic paralysis leading to cardiovascular compromiseDominic O Awuah, Murtaza S Hussain, Anoosha Ponnapalli, Smit Sunil Deliwala, Elfateh M Seedahmed, Ghassan BachuwaBMJ Case Reports CP Feb 2022, 15 (2) e246674; DOI: 10.1136/bcr-2021-246674
- Diagnostic and management considerations in pseudohypoaldosteronism type 1bJelte Kelchtermans, Sara E Pinney, Jacqueline M M Leonard, Sharon Mcgrath-MorrowBMJ Case Reports CP Jan 2022, 15 (1) e246538; DOI: 10.1136/bcr-2021-246538
- Topiramate-induced severe electrolyte abnormalities and hypernatremia leading to central pontine myelinolysisLuba Muaddi, Omar Osman, Barbara ClarkBMJ Case Reports CP Nov 2021, 14 (11) e245870; DOI: 10.1136/bcr-2021-245870
- Severe refeeding syndrome after human chorionic gonadotropin diet: a potentially lethal complicationMax J Schunemann, Martina Bertschinger, Christian Trachsel, Esther BachliBMJ Case Reports CP Nov 2021, 14 (11) e244011; DOI: 10.1136/bcr-2021-244011
- MELAS syndrome: an acute stroke-like episode complicated by renal tubular acidosisDearbhail Ni Cathain, Emmet Browne, Kieran Skehan, Karl BoyleBMJ Case Reports CP Nov 2021, 14 (11) e245898; DOI: 10.1136/bcr-2021-245898
- Antenatal Bartter syndrome: a new compound heterozygous mutation in exon 2 of KCNJ1 geneSrinivasan Mani, Jayasree Nair, Deepali HandaBMJ Case Reports CP Oct 2021, 14 (10) e244685; DOI: 10.1136/bcr-2021-244685
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