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slc12a3 (65) 65
humans (62) 62
gitelman syndrome (53) 53
index medicus (52) 52
female (46) 46
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slc12a3 gene (42) 42
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solute carrier family 12, member 3 - genetics (26) 26
na-cl cotransporter (25) 25
symporters - genetics (25) 25
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Journal of Maternal-Fetal and Neonatal Medicine, ISSN 1476-7058, 2019, pp. 1 - 3
We report a case of a 30-year-old woman who was first found to have a persistently low serum potassium level at 26 years of age during her first pregnancy.... 
Gitelman syndrome | SLC12A3 gene | hypokalemia | pregnancy
Journal Article
ENDOCRINE JOURNAL, ISSN 0918-8959, 2015, Volume 62, Issue 1, pp. 29 - 36
Abstract. Gitelman syndrome (GS) is a salt-wasting tubulointerstitial disease of autosomal recessive inheritance (OMIM613395) caused by genic mutation of... 
Journal Article
Endocrine Journal, ISSN 0918-8959, 2015, Volume 62, Issue 1, pp. 29 - 36
Gitelman syndrome (GS) is a salt-wasting tubulointerstitial disease of autosomal recessive inheritance (OMIM613395) caused by genic mutation of SLC12A3, which... 
Gitelman syndrome | SLC12A3 gene | Mutation
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 | Hypokalemia/blood | Angiotensin-Converting Enzyme Inhibitors/therapeutic use | Diagnosis, Differential | Anti-Inflammatory Agents, Non-Steroidal/therapeutic use | Genetic Testing | Bartter Syndrome/blood | Chloride Channels/genetics | Potassium/administration & dosage | Humans | Consensus Development Conferences as Topic | Rare Diseases/genetics | Sodium Chloride, Dietary/therapeutic use | Gitelman Syndrome/complications | Phenotype | Solute Carrier Family 12, Member 3/genetics | Ultrasonography | Calcium/urine | Quality of Life | Magnesium/administration & dosage | Angiotensin Receptor Antagonists/therapeutic use | Mutation | Chondrocalcinosis/etiology | Dietary Supplements | Practice Guidelines as Topic | 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 | Hypokalemia - blood | Magnesium - administration & dosage | 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 | Bartter Syndrome - blood | Chondrocalcinosis - prevention & control | Sodium Chloride, Dietary - therapeutic use | Calcium - urine | Magnesium - therapeutic use | Anti-Inflammatory Agents, Non-Steroidal - therapeutic use | Potassium - administration & dosage | Chondrocalcinosis - etiology | Potassium - therapeutic use | Gitelman Syndrome - complications | Gitelman Syndrome - diagnosis | Potassium - blood | Gitelman Syndrome - genetics | Angiotensin Receptor Antagonists - therapeutic use | Hypokalemia - genetics | Magnesium - blood
Journal Article
by Zhong, F and Zhong, F and Ying, H and Ying, H and Jia, W and Jia, W and Zhou, X and Zhou, X and Zhang, H and Zhang, H and Guan, Q and Guan, Q and Xu, J and Xu, J and Fang, L and Fang, L and Zhao, J and Zhao, J and Xu, C and Xu, C
Journal of Endocrinological Investigation, ISSN 0391-4097, 6/2019, Volume 42, Issue 6, pp. 653 - 665
Journal Article
Kidney International, ISSN 0085-2538, 01/2017, Volume 91, Issue 1, p. 24
Gitelman syndrome (GS) is a rare, salt-losing tubulopathy characterized by hypokalemic metabolic alkalosis with hypomagnesemia and hypocalciuria. The disease... 
SLC12A3 | thiazide-sensitive sodium-chloride cotransporter | salt-losing tubulopathy | hypokalemic metabolic alkalosis | hypomagnesemia | Journal Article
Journal Article
NEFROLOGÍA, ISSN 0211-6995, 07/2017, Volume 37, Issue 4, pp. 423 - 428
Gitelman's syndrome (GS) is an autosomal recessive disorder caused by mutations in the gene. GS is characterized by hypokalaemic metabolic alkalosis,... 
SLC12A3 gene | Pacientes de etnia gitana | Roma genetic background | Gypsy patients | Gitelman's syndrome | Síndrome de Gitelman | Antecedentes genéticos gitanos | Gen SLC12A3 | GENE | GREATER-THAN-T | COTRANSPORTER | UROLOGY & NEPHROLOGY | EXPLAINS
Journal Article
Journal of the American Society of Nephrology, ISSN 1046-6673, 06/2017, Volume 28, Issue 6, pp. 1814 - 1825
Journal Article
Nefrología, ISSN 0211-6995, 07/2017, Volume 37, Issue 4, pp. 423 - 428
Background: Gitelman's syndrome (GS) is an autosomal recessive disorder caused by mutations in the SLC12A3 gene. GS is characterized by hypokalaemic metabolic... 
SLC12A3 gene | Roma genetic background | Gypsy patients | Gitelman's syndrome
Journal Article
Therapeutics and Clinical Risk Management, ISSN 1176-6336, 01/2018, Volume 14, pp. 149 - 155
Journal Article
Electrolytes & Blood Pressure, ISSN 1738-5997, 2016, Volume 14, Issue 1, p. 16
A 42-year-old man came to the hospital presenting chest discomfort and general weakness. He had come to the hospital with the same symptoms 3 months ago and 12... 
SLC12A3 gene | Gitelman`s syndrome | Hypokalemia | Hypomagnesemia
Journal Article
Journal Article
by Li, Z and Zhao, TY and Tan, XH and Lei, S and Huang, L and Yang, L
INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, ISSN 1660-4601, 09/2019, Volume 16, Issue 17, p. 3207
Unfavorable serum lipid levels are the most important risk factors for coronary artery disease (CAD), cerebral infarction, and other cardiovascular and... 
SLC12A3 | FAMILIAL HYPERCHOLESTEROLEMIA | CHOLESTEROL | PCSK9 | RISK | GENETIC-VARIANTS | LOCI | plasma lipid levels | ENVIRONMENTAL SCIENCES | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | METABOLISM | dyslipidemia | CORONARY-HEART-DISEASE | LDLR
Journal Article
NEFROLOGIA (English Edition), ISSN 2013-2514, 07/2017, Volume 37, Issue 4, pp. 423 - 428
Gitelman's syndrome (GS) is an autosomal recessive disorder caused by mutations in the gene. GS is characterized by hypokalaemic metabolic alkalosis,... 
SLC12A3 gene | Pacientes de etnia gitana | Roma genetic background | Gypsy patients | Gitelman's syndrome | Síndrome de Gitelman | Antecedentes genéticos gitanos | Gen SLC12A3
Journal Article
Nefrologia, 07/2017, Volume 37, Issue 4, pp. 423 - 428
Background: Gitelman's syndrome (GS) is an autosomal recessive disorder caused by mutations in the SLC12A3 gene. GS is characterized by hypokalaemic metabolic... 
SLC12A3 gene | Roma genetic background | Gypsy patients | Gitelman's syndrome
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 09/2004, Volume 24, Issue 36, pp. 7931 - 7938
Journal Article
Electrolyte and Blood Pressure, ISSN 1738-5997, 06/2016, Volume 14, Issue 1, pp. 16 - 19
A 42-year-old man came to the hospital presenting chest discomfort and general weakness. He had come to the hospital with the same symptoms 3 months ago and 12... 
Hypokalemia | SLC12A3 gene | Gitelman's syndrome | Hypomagnesemia | Case Report
Journal Article
Genetics and Molecular Research, 12/2017, Volume 16, Issue 4, p. 1
Gitelman syndrome (GS) is a genetic disorder that affects kidney and causes an imbalance of charged atoms (ions) in the body, including ions of potassium,... 
Gitelman syndrome | SLC12A3 gene | Exome sequencing | Saudi family | Databases | Calcium | Hypokalemia | Magnesium | Mutation | Population genetics | Genetic counselling | Alkalosis
Journal Article
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