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1                                              Gitelman syndrome is a salt-losing tubulopathy caused by
2                                              Gitelman syndrome is a salt-losing tubulopathy character
3                                              Gitelman syndrome is caused by biallelic pathogenic vari
4                                              Gitelman syndrome is the most frequent hereditary salt-l
5 tDNA variants in MT-TF and MT-TI can cause a Gitelman-like syndrome.
6  approximately 10 percent of patients with a Gitelman syndrome phenotype, the genotype is unknown.
7  distal convoluted tubule can cause acquired Gitelman syndrome.
8  including hypokalaemic metabolic alkalosis; Gitelman's syndrome represents the predominant subset of
9 requently observed disorders are Bartter and Gitelman syndrome, which affect salt transport in the th
10 hloride cotransporter gene (NCCT or TSC) and Gitelman's syndrome (GS).
11 g loss, and the genetic disorders Andermann, Gitelman, and Bartter syndromes.
12 -seven genotyped SLT patients (with Bartter, Gitelman or EAST Syndromes) are recruited.
13 contrast, recombinants were observed between Gitelman's syndrome and the flanking markers D16S419 and
14 Na-Cl cotransporter have been shown to cause Gitelman's syndrome.
15  (NCC) of the distal convoluted tubule cause Gitelman's syndrome, an inherited hypokalemic alkalosis
16 ns in the NCC cause the salt-wasting disease Gitelman syndrome(4).
17 utosomal dominant polycystic kidney disease, Gitelman syndrome, Bartter syndrome, autosomal recessive
18 r's and Bartter's-like syndromes, especially Gitelman's, has come largely as a result of the advances
19 described for tubulopathies such as Fanconi, Gitelman, and Bartter-like syndromes and renal tubular a
20 ld be considered in diagnostic workflows for Gitelman syndrome.
21 lood pressure can be divided into two groups-Gitelman's syndrome, featuring hypocalciuria, hypomagnes
22 ercalciuria, and/or polyuria), and 26.0% had Gitelman-like syndrome (fortuitous discovery of hypokale
23 nt; and (3) the hypocalciuric-hypomagnesemic Gitelman variant.
24 enal salt wasting with arterial hypotension (Gitelman syndrome).
25 mportant part of the missing heritability in Gitelman syndrome.
26 -K-2Cl cotransporter (NKCC2) are involved in Gitelman and Bartter syndrome, respectively, autosomal r
27 of Mg2+ and Ca2+ are altered, as observed in Gitelman's syndrome.
28 nt in WNK4(-/-) mice, which exhibited a mild Gitelman-like syndrome, with normal blood pressure, incr
29 splay hypomagnesemia, which sometimes mimics Gitelman syndrome.
30  findings demonstrate the molecular basis of Gitelman's syndrome.
31 ain knock-in mice showed typical features of Gitelman Syndrome with mild hypokalaemia, hypomagnesaemi
32       We now demonstrate complete linkage of Gitelman's syndrome to the locus encoding the renal thia
33 olume homeostasis and in the pathogenesis of Gitelman's syndrome, we used gene targeting to prepare a
34 10 may result in the same renal phenotype of Gitelman syndrome, as they can lead to reduced NCC activ
35 be responsible for the clinical phenotype of Gitelman's syndrome, a variant of Bartter's syndrome.
36  hypocalciuria and hypercalcemia, suggesting Gitelman syndrome (GS).
37  DNA samples from individuals with suspected Gitelman syndrome in whom a single likely pathogenic or
38 re were no recombinants observed between the Gitelman's syndrome phenotype and inheritance of D16S408
39 e clinical phenotype of PHAII is opposite to Gitelman syndrome, a disease caused by dysfunction of th
40           Mutations in NCC also give rise to Gitelman syndrome, a hereditary salt-wasting disorder th
41 d be considered in patients with unexplained Gitelman syndrome-like tubulopathies.
42  DNA (mtDNA) variants in three families with Gitelman-like electrolyte abnormalities, then investigat
43 the latter is defective in this kindred with Gitelman's syndrome.
44 ied mitochondrial mutations in patients with Gitelman or Fanconi syndrome.
45                                Patients with Gitelman syndrome (GS), an inherited salt-losing tubulop
46                                Patients with Gitelman syndrome had lower systolic BP and higher heart
47  testing, approximately 14% of patients with Gitelman syndrome were prediabetic, compared with 5% of
48                In up to 10% of patients with Gitelman syndrome, current genetic techniques detect onl
49 med a cross-sectional study of patients with Gitelman syndrome, heterozygous carriers, and healthy no
50 82 healthy noncarriers, and 79 patients with Gitelman syndrome.
51 hat of healthy noncarriers and patients with Gitelman syndrome.
52 transporter (NCC) is common in patients with Gitelman's syndrome (GS).