Year 2011,
Volume: 8 Issue: 2, - , 01.06.2011
Abstract
Keywords
References
- Gitelman HJ, Graham JB, Welt LG. A new familial disor- der characterized by hypokalemia and hypomagnesemia. Trans Assoc Am Physicians 1966;79:221-35
- Rudin A. Bartter’s syndrome: a review of 28 patients fol- lowed for 10 years. Acta Med Scand 1988;224:165–71.
- Ng HY, Lin SH, Hsu CY, Tsai YZ, Chen HC, Lee CT. Hypokalemic paralysis due to Gitelman syndrome: A fam- ily study. Neurology 2006;67:1080–2
- Shaer AJ. Inherited Primary Renal Tubular Hypokalemic Alkalosis: A Review of Gitelman and Bartter Syndromes. Am J Med Sci 2001;322:316–32
- Knoers NV, Levtchenko EN. Gitelman syndrome. Orphanet Journal of Rare Diseases 2008;3:22
- Rodriguez-Soriano J. Bartter and related syndromes: the puzzle is almost solved. Pediatr Nephrol 1998;12:315-27
- Liaw LC, Banerjee K, Coulthard MG. Dose related growth response to indometacin in Gitelman syndrome. Arch Dis Child 1999;81:508–10
- Simon DB, Nelson-Williams C, Bia MJ, et al. Gitelman's variant of Barrter's syndrome, inherited hypokalaemic al- kalosis, is caused by mutations in the thiazide-sensitive Na−Cl cotransporter. Nature Genetic 1996;12:24-30
- Lee Y, Wang I, Lin T, Huang C. Gitelman syndrome: report of three cases and literature review. Kaohsiung J Med Sci 2006;22:357–62
- Monnens L, Bindels R, Grunfeld JP. Gitelman syndrome comes of age. Nephrol Dial Transplant 1998;3:1617–9
- Kokko JP. Cecil Textbook of Medicine. In:Goldman L, Ausiello D, ed. Fluids and Electrolytes. 22nd ed. Philadelphia: Saunders; 2004: 683-5
Year 2011,
Volume: 8 Issue: 2, - , 01.06.2011
Abstract
-
Keywords
References
- Gitelman HJ, Graham JB, Welt LG. A new familial disor- der characterized by hypokalemia and hypomagnesemia. Trans Assoc Am Physicians 1966;79:221-35
- Rudin A. Bartter’s syndrome: a review of 28 patients fol- lowed for 10 years. Acta Med Scand 1988;224:165–71.
- Ng HY, Lin SH, Hsu CY, Tsai YZ, Chen HC, Lee CT. Hypokalemic paralysis due to Gitelman syndrome: A fam- ily study. Neurology 2006;67:1080–2
- Shaer AJ. Inherited Primary Renal Tubular Hypokalemic Alkalosis: A Review of Gitelman and Bartter Syndromes. Am J Med Sci 2001;322:316–32
- Knoers NV, Levtchenko EN. Gitelman syndrome. Orphanet Journal of Rare Diseases 2008;3:22
- Rodriguez-Soriano J. Bartter and related syndromes: the puzzle is almost solved. Pediatr Nephrol 1998;12:315-27
- Liaw LC, Banerjee K, Coulthard MG. Dose related growth response to indometacin in Gitelman syndrome. Arch Dis Child 1999;81:508–10
- Simon DB, Nelson-Williams C, Bia MJ, et al. Gitelman's variant of Barrter's syndrome, inherited hypokalaemic al- kalosis, is caused by mutations in the thiazide-sensitive Na−Cl cotransporter. Nature Genetic 1996;12:24-30
- Lee Y, Wang I, Lin T, Huang C. Gitelman syndrome: report of three cases and literature review. Kaohsiung J Med Sci 2006;22:357–62
- Monnens L, Bindels R, Grunfeld JP. Gitelman syndrome comes of age. Nephrol Dial Transplant 1998;3:1617–9
- Kokko JP. Cecil Textbook of Medicine. In:Goldman L, Ausiello D, ed. Fluids and Electrolytes. 22nd ed. Philadelphia: Saunders; 2004: 683-5
There are 11 citations in total.
Details
| Primary Language | English |
|---|---|
| Journal Section | Case Report |
| Authors | |
| Publication Date | June 1, 2011 |
| Published in Issue | Year 2011 Volume: 8 Issue: 2 |