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Academic Journal

Gitelman syndrome patient managed with amiloride during pregnancy and lactation.

  • Authors : Ibrahim A; Nephrology Division, Department of Internal Medicine, University of Utah Health, Salt Lake City, USA.; Rodan AR

Subjects: Gitelman Syndrome*/Gitelman Syndrome*/Gitelman Syndrome*/drug therapy ; Gitelman Syndrome*/Gitelman Syndrome*/Gitelman Syndrome*/complications ; Gitelman Syndrome*/Gitelman Syndrome*/Gitelman Syndrome*/diagnosis

  • Source: BMC nephrology [BMC Nephrol] 2024 Nov 09; Vol. 25 (1), pp. 403. Date of Electronic Publication: 2024 Nov 09.Publisher: BioMed Central Country of Publication: England NLM ID: 100967793 Publication Model: Electronic Cited Medium:

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Academic Journal

Gitelman syndrome with Graves' disease leading to rhabdomyolysis: a case report and literature review.

  • Authors : Xu J; Department of Endocrinology and Metabolism, the Affiliated Hospital of Guizhou Medical University, Guiyang, 550004, China.; He J

Subjects: Gitelman Syndrome*/Gitelman Syndrome*/Gitelman Syndrome*/complications ; Gitelman Syndrome*/Gitelman Syndrome*/Gitelman Syndrome*/diagnosis ; Gitelman Syndrome*/Gitelman Syndrome*/Gitelman Syndrome*/genetics

  • Source: BMC nephrology [BMC Nephrol] 2023 May 02; Vol. 24 (1), pp. 123. Date of Electronic Publication: 2023 May 02.Publisher: BioMed Central Country of Publication: England NLM ID: 100967793 Publication Model: Electronic Cited Medium:

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Academic Journal

A case of Gitelman syndrome with membranous nephropathy.

  • Authors : Guo X; Department of Nephrology, Linping Campus, The Second Affiliated Hospital of Zhejiang University School of Medicine, No.369, Yingbin Road, Linping District, 311199, Zhejiang, Hangzhou, People's Republic of China.; Yu S

Subjects: Gitelman Syndrome*/Gitelman Syndrome*/Gitelman Syndrome*/complications ; Gitelman Syndrome*/Gitelman Syndrome*/Gitelman Syndrome*/diagnosis ; Gitelman Syndrome*/Gitelman Syndrome*/Gitelman Syndrome*/genetics

  • Source: BMC nephrology [BMC Nephrol] 2022 Jul 26; Vol. 23 (1), pp. 267. Date of Electronic Publication: 2022 Jul 26.Publisher: BioMed Central Country of Publication: England NLM ID: 100967793 Publication Model: Electronic Cited Medium:

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Academic Journal

Gitelman syndrome with normocalciuria - a case report.

  • Authors : Flisiński M; Department of Nephrology, Hypertension and Internal Medicine, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, ul. Curie-Skłodowskiej 9, 85-094, Bydgoszcz, Poland. .; Skalska E

Subjects: Alkalosis*/Alkalosis*/Alkalosis*/genetics ; Gitelman Syndrome*/Gitelman Syndrome*/Gitelman Syndrome*/complications ; Gitelman Syndrome*/Gitelman Syndrome*/Gitelman Syndrome*/diagnosis

  • Source: BMC nephrology [BMC Nephrol] 2022 May 04; Vol. 23 (1), pp. 170. Date of Electronic Publication: 2022 May 04.Publisher: BioMed Central Country of Publication: England NLM ID: 100967793 Publication Model: Electronic Cited Medium:

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Academic Journal

A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome with diabetes and the choices of the appropriate hypoglycemic drugs: a case report.

  • Authors : Liu Z; Department of Nephrology, The Affiliated Qingdao Municipal Hospital of Qingdao University, No. 5 Donghai Middle Road, Qingdao, 266071, People's Republic of China.; Wang S

Subjects: Gitelman Syndrome*/Gitelman Syndrome*/Gitelman Syndrome*/genetics ; Gitelman Syndrome*/Gitelman Syndrome*/Gitelman Syndrome*/drug therapy ; Gitelman Syndrome*/Gitelman Syndrome*/Gitelman Syndrome*/complications

  • Source: BMC medical genomics [BMC Med Genomics] 2021 Aug 04; Vol. 14 (1), pp. 198. Date of Electronic Publication: 2021 Aug 04.Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium:

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Academic Journal

Different roles of the RAAS affect bone metabolism in patients with primary aldosteronism, Gitelman syndrome and Bartter syndrome.

  • Authors : Tang W; Endocrinology and Metabolism Disease Department, Tianjin Medical University General Hospital, 154# Anshan Road, Heping District, Tianjin, 300052, China.; Chai Y

Subjects: Bartter Syndrome/Bartter Syndrome/Bartter Syndrome/*metabolism ; Bone and Bones/Bone and Bones/Bone and Bones/*metabolism ; Gitelman Syndrome/Gitelman Syndrome/Gitelman Syndrome/*metabolism

  • Source: BMC endocrine disorders [BMC Endocr Disord] 2022 Feb 11; Vol. 22 (1), pp. 38. Date of Electronic Publication: 2022 Feb 11.Publisher: BioMed Central Country of Publication: England NLM ID: 101088676 Publication Model: Electronic Cited Medium:

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Academic Journal

Early onset children's Gitelman syndrome with severe hypokalaemia: a case report.

  • Authors : Chen H; Department of Paediatrics, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, 88 Changling Road, Xiqing district, Tianjin, 300000, China. .; Ma R

Subjects: Bartter Syndrome*/Bartter Syndrome*/Bartter Syndrome*/complications ; Bartter Syndrome*/Bartter Syndrome*/Bartter Syndrome*/diagnosis ; Bartter Syndrome*/Bartter Syndrome*/Bartter Syndrome*/genetics

  • Source: BMC pediatrics [BMC Pediatr] 2020 Aug 05; Vol. 20 (1), pp. 366. Date of Electronic Publication: 2020 Aug 05.Publisher: BioMed Central Country of Publication: England NLM ID: 100967804 Publication Model: Electronic Cited Medium:

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Academic Journal

Kidney stones and moderate proteinuria as the rare manifestations of Gitelman syndrome.

  • Authors : Chen Q; Department of Nephrology, The First People's Hospital of Huzhou, 313000, Huzhou, Zhejiang, People's Republic of China.; Wang X

Subjects: Gitelman Syndrome/Gitelman Syndrome/Gitelman Syndrome/*complications ; Kidney Calculi/Kidney Calculi/Kidney Calculi/*etiology ; Proteinuria/Proteinuria/Proteinuria/*etiology

  • Source: BMC nephrology [BMC Nephrol] 2021 Jan 07; Vol. 22 (1), pp. 12. Date of Electronic Publication: 2021 Jan 07.Publisher: BioMed Central Country of Publication: England NLM ID: 100967793 Publication Model: Electronic Cited Medium:

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Academic Journal

Identification of compound mutations of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome exhibiting Bartter syndrome-liked phenotypes.

  • Authors : Dong B; Department of Endocrinology and Metabolism, the Affiliated Hospital of Qingdao University, 16 Jiangsu Road, Qingdao, 266003, China.; Chen Y

Subjects: Gitelman Syndrome/Gitelman Syndrome/Gitelman Syndrome/*genetics; Adult ; Aged

  • Source: BMC nephrology [BMC Nephrol] 2020 Aug 05; Vol. 21 (1), pp. 328. Date of Electronic Publication: 2020 Aug 05.Publisher: BioMed Central Country of Publication: England NLM ID: 100967793 Publication Model: Electronic Cited Medium:

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Academic Journal

Digenetic inheritance of SLC12A3 and CLCNKB genes in a Chinese girl with Gitelman syndrome.

  • Authors : Kong Y; The First Affiliated Hospital of Zhejiang University, Hangzhou, China.; Xu K

Subjects: Genetic Predisposition to Disease* ; Mutation*; Chloride Channels/Chloride Channels/Chloride Channels/*genetics

  • Source: BMC pediatrics [BMC Pediatr] 2019 Apr 18; Vol. 19 (1), pp. 114. Date of Electronic Publication: 2019 Apr 18.Publisher: BioMed Central Country of Publication: England NLM ID: 100967804 Publication Model: Electronic Cited Medium:

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  • 1-10 of  115 results for ""GITELMAN syndrome""