about
Regulator of G Protein Signaling 2: A Versatile Regulator of Vascular FunctionBartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects.Identification of two novel mutations in SLC12A3 gene in two Chinese pedigrees with Gitelman syndrome and review of literature.Molecular pathophysiology of Bartter's and Gitelman's syndromes.Genetic causes of hypomagnesemia, a clinical overviewCurrent views on the diagnosis and management of hypokalaemia in children.The WNKs: atypical protein kinases with pleiotropic actions.Recurrent deep intronic mutations in the SLC12A3 gene responsible for Gitelman's syndromeIndomethacin, amiloride, or eplerenone for treating hypokalemia in Gitelman syndromeA severe phenotype of Gitelman syndrome with increased prostaglandin excretion and favorable response to indomethacin.A pseudo-dominant form of Gitelman's syndrome.The thiazide-sensitive NaCl cotransporter is targeted for chaperone-dependent endoplasmic reticulum-associated degradation.Gitelman syndrome in a South African family presenting with hypokalaemia and unusual food cravings.Gitelman syndrome manifesting in early childhood and leading to delayed puberty: a case report.Two cases of successful pregnancy in patients with Gitelman's syndrome.Outpatient management of Gitelman's syndrome in pregnancy.Gitelman or Bartter type 3 syndrome? A case of distal convoluted tubulopathy caused by CLCNKB gene mutation.An Adult Case of Bartter Syndrome Type III Presenting with Proteinuria.Clinical Analysis of a Hypokalemic Salt-losing Tubulopathy CasePhosphorylation regulates NCC stability and transporter activity in vivoAnesthesia in a patient with gitelman syndromeA novel homozygous mutation in the solute carrier family 12 member 3 gene in a Chinese family with Gitelman syndrome.Hyponatremia - A rare complication of Gitelman's syndrome.Does stress induce salt intake?Gitelman syndrome: pathophysiological and clinical aspects.A man with a worrying potassium deficiencyVasopressin regulation of sodium transport in the distal nephron and collecting duct.Novel brain MRI abnormalities in Gitelman syndrome.Management of a severe case of Gitelman syndrome with poor response to standard treatment.Ion transport in the zebrafish kidney from a human disease angle: possibilities, considerations, and future perspectives.Analysis of mutations of two Gitelman syndrome family SLC12A3 genes and proposed treatments using Chinese medicine.Disease modeling in genetic kidney diseases: mice.Gitelman syndrome: an analysis of the underlying pathophysiologic mechanisms of acid-base and electrolyte abnormalities.A case of Gitelman syndrome with severe hyponatraemia and hypophosphataemia.Localised normocalcaemic tetany secondary to dehydration in an individual with Gitelman syndromeBartter and Gitelman syndromes: Spectrum of clinical manifestations caused by different mutations.Chondrocalcinosis and Gitelman syndrome.New SLC12A3 disease causative mutation of Gitelman's syndrome.Gitelman's syndrome with persistent hypokalemia - don't forget licorice, alcohol, lemon juice, iced tea and salt depletion: a case reportCase Report: Cervical chondrocalcinosis as a complication of Gitelman syndrome.
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
name
Gitelman syndrome
@ast
Gitelman syndrome
@en
Gitelman syndrome
@en-gb
Gitelman syndrome
@nl
type
label
Gitelman syndrome
@ast
Gitelman syndrome
@en
Gitelman syndrome
@en-gb
Gitelman syndrome
@nl
prefLabel
Gitelman syndrome
@ast
Gitelman syndrome
@en
Gitelman syndrome
@en-gb
Gitelman syndrome
@nl
P2860
P921
P3181
P356
P1476
Gitelman syndrome
@en
P2093
Elena N Levtchenko
Nine V A M Knoers
P2860
P2888
P3181
P356
10.1186/1750-1172-3-22
P407
P5008
P577
2008-07-30T00:00:00Z
P5875
P6179
1007660001