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146 results on '"Gitelman Syndrome complications"'

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1. Gitelman syndrome and in vitro fertilization-embryo transfer: advancing preconception care in nephrology.

2. Gitelman syndrome patient managed with amiloride during pregnancy and lactation.

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3. Clinical Features and Unusual Heterozygous Mutations in Patients with Renal Hypokalemia.

4. A case of pseudo-Bartter/Gitelman syndrome caused by long-term laxative abuse, leading to end-stage kidney disease.

5. A novel homozygous SLC12A3 mutation causing Gitelman syndrome with co-existent autoimmune thyroiditis: a case report and review of the literature.

6. Concurrent Gitelman Syndrome and Hyperthyroidism: Diagnostic Challenges in a 51-Year-Old Patient.

7. Gitelman syndrome with primary hyperparathyroidism: A case report.

8. Adult classic Bartter syndrome: a case report with 5-year follow-up and literature review.

9. Interpreting epigenetic causes of recurrent hypokalemia and seizures: Gitelman syndrome co-exist with pseudohypoparathyroidism type 1B.

10. Clinical and genetic analysis of a case of Gitelman syndrome accompanied with Graves disease and adrenocortical adenoma: A case report.

11. Hypokalemia Induced Partial Nephrogenic Diabetes Insipidus: A Case Report.

13. Gitelman syndrome combined with diabetes mellitus: A case report and literature review.

15. Case report: Gitelman syndrome with diabetes: Confirmed by both hydrochlorothiazide test and genetic testing.

16. Gitelman syndrome with Graves' disease leading to rhabdomyolysis: a case report and literature review.

18. Tophaceous gout in a young man with Gitelman syndrome: a case report with an overview.

19. Clinicopathological Features of Gitelman Syndrome with Proteinuria and Renal Dysfunction.

20. Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study.

21. The genetic spectrum of Gitelman(-like) syndromes.

22. Molecular diagnosis of adult patients with clinically unexplained hypokalemia without hypertension demonstrated a diagnostic yield of 30.5.

23. A case of Gitelman syndrome with membranous nephropathy.

24. Calcium pyrophosphate crystal deposition in a cohort of 57 patients with Gitelman syndrome.

25. Gitelman syndrome with normocalciuria - a case report.

26. Gitelman syndrome with a novel frameshift variant in SLC12A3 gene accompanied by chronic kidney disease and type 2 diabetes mellitus.

27. Rapidly Progressing to ESRD in an Individual with Coexisting ADPKD and Masked Klinefelter and Gitelman Syndromes.

28. Difficulties in the management of hypokalemia in a pregnant patient with Gitelman syndrome.

31. Anesthetic management of child with Gitelman Syndrome: case report.

32. A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome with diabetes and the choices of the appropriate hypoglycemic drugs: a case report.

33. Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations.

34. Phenotypic differences of mutation-negative cases in Gitelman syndrome clinically diagnosed in adulthood.

35. Type-5 Bartter syndrome presenting with metabolic seizure in adulthood.

36. Kidney stones and moderate proteinuria as the rare manifestations of Gitelman syndrome.

37. Genetic Analysis of Gitelman Syndrome: Co-existence with Hyperthyroidism in a Two-year-old Boy.

38. [Renal involvement in Sjögren's syndrome].

39. QT Interval in Adult with Chronic Hypokalemia due to Gitelman Syndrome: Not so Frequently Prolonged.

40. [A delicate balance: Gitelman syndrome and gestational diabetes. A case report].

41. Early onset children's Gitelman syndrome with severe hypokalaemia: a case report.

42. Type 2 diabetes mellitus caused by Gitelman syndrome-related hypokalemia: A case report.

43. Orthotopic Heart Transplantation in a Patient With Gitelman Syndrome and Dilated Cardiomyopathy.

44. [Bartter-Gitelman syndromes].

45. Gitelman syndrome associated with chondrocalcinosis and severe neuropathy: a novel heterozygous mutation in SLC12A3 gene.

47. A Case of Gitelman Syndrome Diagnosed with Anorexia Nervosa in a Psychiatry Clinic.

48. Bilateral hamstring origin calcification: rare presentation of Gitelman syndrome.

49. Persistent hypokalemia due to a rare mutation in gitelman's syndrome.

50. Ventricular arrhythmia and tachycardia-induced cardiomyopathy in Gitelman syndrome, hypokalaemia is not the only culpable.