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A novel compound heterozygous mutation of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome.

• Authors : Wang X; Department of Rheumatology, Shaoxing People's Hospital (Shaoxing Hospital, Zhejiang University School of Medicine), 312000, Shaoxing, People's Republic of China.; Ding Y

Subjects: Gitelman Syndrome*/Gitelman Syndrome*/Gitelman Syndrome*/genetics; China ; Humans

• Source: Endocrine [Endocrine] 2020 Mar; Vol. 67 (3), pp. 673-677. Date of Electronic Publication: 2019 Dec 05.Publisher: Humana Press Country of Publication: United States NLM ID: 9434444 Publication Model: Print-Electronic Cited

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Gitelman's syndrome: a pathophysiological and clinical update.

• Authors : Nakhoul F; Nephrology & Hypertension Division, Faculty of Medicine, Baruch-Padeh Poryia Medical Center, Lower Galilee, Israel. ; Nakhoul N

Subjects: Gitelman Syndrome/Gitelman Syndrome/Gitelman Syndrome/*genetics ; Gitelman Syndrome/Gitelman Syndrome/Gitelman Syndrome/*physiopathology ; Mutation/Mutation/Mutation/*genetics

• Source: Endocrine [Endocrine] 2012 Feb; Vol. 41 (1), pp. 53-7. Date of Electronic Publication: 2011 Nov 15.Publisher: Humana Press Country of Publication: United States NLM ID: 9434444 Publication Model: Print-Electronic Cited

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Two novel genotypes of the thiazide-sensitive Na-Cl cotransporter (SLC12A3) gene in patients with Gitelman's syndrome.

• Authors : Aoi N; Division of Nephrology and Endocrinology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.; Nakayama T

Subjects: Polymorphism, Single Nucleotide*; Gitelman Syndrome/Gitelman Syndrome/Gitelman Syndrome/*genetics ; Receptors, Drug/Receptors, Drug/Receptors, Drug/*genetics

• Source: Endocrine [Endocrine] 2007 Apr; Vol. 31 (2), pp. 149-53.Publisher: Humana Press Country of Publication: United States NLM ID: 9434444 Publication Model: Print Cited Medium:

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Screening and diagnosis of primary aldosteronism. Consensus document of all the Spanish Societies involved in the management of primary aldosteronism.

• Authors : Araujo-Castro M; Ruiz-Sánchez JG ...

Subjects: Hyperaldosteronism*/Hyperaldosteronism*/Hyperaldosteronism*/diagnosis ; Hyperaldosteronism*/Hyperaldosteronism*/Hyperaldosteronism*/therapy; Humans

• Source: Endocrine [Endocrine] 2024 Jul; Vol. 85 (1), pp. 99-121. Date of Electronic Publication: 2024 Mar 06.Publisher: Humana Press Country of Publication: United States NLM ID: 9434444 Publication Model: Print-Electronic Cited

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Thirteen novel CLCNKB variants and genotype/phenotype association study in 42 Chinese patients with Bartter syndrome type 3.

• Authors : Han Y; Department of Nephrology, The Affiliated Qingdao Municipal Hospital of Qingdao University, No. 5 Donghai Middle Road, Qingdao, 266071, PR China.; Central Laboratory, The Affiliated Hospital of Qingdao University, Qingdao, 266003, PR China.

Subjects: Bartter Syndrome*/Bartter Syndrome*/Bartter Syndrome*/genetics ; Chloride Channels*/Chloride Channels*/Chloride Channels*/genetics; China

• Source: Endocrine [Endocrine] 2020 Apr; Vol. 68 (1), pp. 192-202. Date of Electronic Publication: 2019 Dec 13.Publisher: Humana Press Country of Publication: United States NLM ID: 9434444 Publication Model: Print-Electronic Cited

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Bioinformatics and Drug Discovery

• Authors : Larson, Richard S.

Subjects: Medical personnel; Physical sciences; Pharmaceutical chemistryCOMPUTERS / Data Science / Bioinformatics; MEDICAL / Pharmacology; SCIENCE / Life Sciences / Molecular Biology

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