Results 81 to 90 of about 1,230,526 (158)

Increased endothelial nitric oxide synthase mRNA level in Bartter's and Gitelman's syndrome - Relationship to vascular reactivity

, 1999
AIM: Patients with Bartter's syndrome and Gitelman's syndrome have reduced vascular reactivity, normo-hypotension and decreased peripheral resistances in spite of biochemical and hormonal abnormalities typical of hypertension. Since we found that both
ANTONELLO, AUGUSTO, CALO L, CANTARO S, MILANI M, D'ANGELO, ANGELA, FAVARO, SILVANA, DAVIS PA   +6 more
core  

Supplementary Material for: Genotype/Phenotype Analysis in 67 Chinese Patients with Gitelman's Syndrome

, 2016
Background: Gitelman's syndrome (GS) is an autosomal recessive renal tubular disorder, which is caused by the mutations in SLC12A3. This study was designed to analyze the characteristics of the genotype and phenotype, and follow-up in the largest group ...
Wang C. (2954256), Lu J. (2954250), Zhao X. (2954253), Liu T. (2954244), Shao L. (2954247), Lang Y. (2954259)   +5 more
core   +1 more source

Effects of chemical chaperones on partially retarded NaCl cotransporter mutants associated with Gitelman's syndrome in a mouse cortical collecting duct cell line. [PDF]

, 2004
Contains fulltext : 58625.pdf (Publisher’s version ) (Open Access)BACKGROUND: Epithelial cells lining the distal convoluted tubule express the thiazide-sensitive Na-Cl cotransporter (NCC) that is responsible for the reabsorption of 5-10%
Heuvel, L.P.W.J. van den, Vandewalle, A., Bindels, R.J.M., L. P. W. J. van den Heuvel, M. Goossens, R. J. M. Bindels, Willems, P.H.G.M., A. Vandewalle, Jong, J.C. de, Goossens, M.P.A.A., Knoers, N.V.A.M., P. H. G. M. Willems, N. V. A. M. Knoers, J. C. de Jong   +13 more
core   +1 more source

Gitelman's Syndrome with Mental Retardation

Internal Medicine, 2006
A 56-year-old mentally retarded Japanese woman (intelligence quotient: 49) was admitted to our hospital with the chief complaints of headache, dizziness, vomiting, and lower limb paralysis. Laboratory tests showed severe hypokalemia, metabolic alkalosis, hypomagnesemia, and hypocalciuria. These findings suggested a diagnosis of Gitelman's syndrome (GS).
Morita, Rena, Takeuchi, Kaoru, Nakamura, Akinobu, Tajima, Toshihiro, Kuroda, Yoshihiko   +4 more
openaire   +3 more sources

Genetic variants of thiazide-sensitive NaCl-cotransporter in Gitelman's syndrome and primary hypertension

, 2000
Gitelman's syndrome is an autosomal recessive disorder characterized by electrolyte disturbances and low blood pressure. The disease is caused by homozygous or compound heterozygous inactivating mutations in the thiazide-sensitive NaCl-cotransporter gene
Råstam, Lennart, Hulthén, Lennart, Groop, Leif, Orho-Melander, Marju, Bengtsson Boström, Kristina, Lindblad, Ulf, Melander, Olle   +6 more
core  

PowerPoint Slides for: Genotype/Phenotype Analysis in 67 Chinese Patients with Gitelman's Syndrome

, 2016
Background: Gitelman's syndrome (GS) is an autosomal recessive renal tubular disorder, which is caused by the mutations in SLC12A3. This study was designed to analyze the characteristics of the genotype and phenotype, and follow-up in the largest group ...
Wang C. (2954256), Lu J. (2954250), Zhao X. (2954253), Liu T. (2954244), Shao L. (2954247), Lang Y. (2954259)   +5 more
core   +1 more source

Prevalence of the metabolic syndrome in Chinese adolescents [PDF]

, 2008
Since national figures on the occurrence of metabolic syndrome among Chinese adolescents are lacking, this study aims to estimate its prevalence and distribution among Chinese youngsters.
Yang, X., Kok, F.J., Zhai, F., Li, Y., Piao, J., Zhang, J., Ma, G.   +6 more
core   +1 more source

Relationship between NOX4 level and angiotensin II signaling in Gitelman's syndrome. Implications with hypertension. [PDF]

Int J Clin Exp Med, 2015
Recent evidence showed that endogenous nicotinamide adenine dinucleotide phosphate-oxidase 4 (NOX4) may exert a protective role on the cardiovascular system inducing vasodilation, reduction of blood pressure, and anti-proliferative actions.
Calò LA, Savoia C, Davis PA, Pagnin E, Ravarotto V, Maiolino G.   +5 more
europepmc   +1 more source

Late‐Breaking Abstract Presentations

Pregnancy, Volume 2, Issue S2, September 2026.
wiley   +1 more source

Reduced-complexity syndrome-based TTCM decoding [PDF]

, 2013
The iterative decoder of Turbo Trellis Coded Modulation (TTCM) exchanges extrinsic information between the constituent TCM decoders, which imposes a high computational complexity at the receiver. Therefore we conceive the syndrome-based block decoding of
Ng, Soon Xin, Hanzo, Lajos, Babar, Zunaira   +2 more
core   +1 more source