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Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2008, Volume 3, Issue 1, pp. 22 - 22
Journal Article
Kidney International, ISSN 0085-2538, 01/2017, Volume 91, Issue 1, pp. 24 - 33
Gitelman syndrome (GS) is a rare, salt-losing tubulopathy characterized by hypokalemic metabolic alkalosis with hypomagnesemia and hypocalciuria. The disease... 
hypokalemic metabolic alkalosis | hypomagnesemia | SLC12A3 | thiazide-sensitive sodium-chloride cotransporter | salt-losing tubulopathy | SERUM POTASSIUM | FOLLOW-UP | HYPOKALEMIC ALKALOSIS | THERAPEUTIC APPROACH | BARTTERS-SYNDROME | BLOOD-PRESSURE | NCC GENE | GLUCOSE-METABOLISM | UROLOGY & NEPHROLOGY | CHANNEL GENE | SODIUM-CHLORIDE COTRANSPORTER | Rare Diseases - genetics | Gitelman Syndrome - drug therapy | Genetic Testing | Hypokalemia - blood | Magnesium - administration & dosage | Humans | Bartter Syndrome - diagnosis | Chloride Channels - genetics | Bartter Syndrome - urine | Angiotensin-Converting Enzyme Inhibitors - therapeutic use | Bartter Syndrome - genetics | Solute Carrier Family 12, Member 3 - genetics | Ultrasonography | Bartter Syndrome - blood | Diagnosis, Differential | Chondrocalcinosis - prevention & control | Sodium Chloride, Dietary - therapeutic use | Calcium - urine | Consensus Development Conferences as Topic | Magnesium - therapeutic use | Phenotype | Anti-Inflammatory Agents, Non-Steroidal - therapeutic use | Potassium - administration & dosage | Chondrocalcinosis - etiology | Potassium - therapeutic use | Gitelman Syndrome - complications | Gitelman Syndrome - diagnosis | Quality of Life | Potassium - blood | Gitelman Syndrome - genetics | Mutation | Angiotensin Receptor Antagonists - therapeutic use | Dietary Supplements | Hypokalemia - genetics | Magnesium - blood | Practice Guidelines as Topic
Journal Article
Pediatric Clinics of North America, ISSN 0031-3955, 02/2019, Volume 66, Issue 1, pp. 121 - 134
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 10/2011, Volume 108, Issue 42, pp. 17538 - 17543
Journal Article
JCPSP-JOURNAL OF THE COLLEGE OF PHYSICIANS AND SURGEONS PAKISTAN, ISSN 1022-386X, 03/2017, Volume 27, Issue 3, pp. S30 - S32
Gitelman syndrome (GS) is the most frequently inherited renal salt-wasting tubulointerstitial disease. It follows variable but usually asymptomatic benign... 
Gitelman syndrome | Bartter syndrome | MEDICINE, GENERAL & INTERNAL | Magnesium | Potassium | Metabolic alkalosis | Young Adult | Male | Humans | Gitelman Syndrome - diagnosis
Journal Article
by Huang, K and Dai, YL and Zhang, JW and Zhang, L and Wu, W and Dong, GP and Ullah, R and Fei, Y and Fu, JF
MEDICINE, ISSN 0025-7974, 10/2019, Volume 98, Issue 40, p. e17244
Rationale: Gitelman syndrome (GS) is a rare autosomal recessive hereditary salt-losing tubulopathy caused by loss-of-function mutations in the SLC12A3 gene. It... 
Gitelman syndrome | MEDICINE, GENERAL & INTERNAL | genetic analysis | growth hormone deficiency | therapy
Journal Article
Journal of the American Society of Nephrology, ISSN 1046-6673, 04/2011, Volume 22, Issue 4, pp. 693 - 703
Journal Article
Journal Article
Journal Article
Journal Article
Current Opinion in Pediatrics, ISSN 1040-8703, 04/2017, Volume 29, Issue 2, pp. 179 - 186
Purpose of review The clinical presentations of Bartter's syndrome and Gitelman's syndrome will be reviewed including two most recently described hypokalemic... 
diagnostic and therapeutic management | Gitelman's syndrome | Bartter's syndrome | clinical presentations | physiologic and pharmacologic classification | HYPERPARATHYROIDISM | COTRANSPORTER | PEDIATRICS | MUTATIONS | NKCC2 | HYPOKALEMIA
Journal Article
Clinical Endocrinology, ISSN 0300-0664, 01/2016, Volume 84, Issue 1, pp. 149 - 150
Journal Article
American Journal of Kidney Diseases, ISSN 0272-6386, 11/2017, Volume 70, Issue 5, pp. 725 - 728
Journal Article