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Journal Abstract Search

187 related items for PubMed ID: 34941636

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  • 5. Novel compound heterozygous mutation of SLC12A3 in Gitelman syndrome co-existent with hyperthyroidism: A case report and literature review.
    Qin YZ, Liu YM, Wang Y, You C, Li LN, Zhou XY, Lv WM, Hong SH, Xiao LX.
    World J Clin Cases; 2022 Jul 26; 10(21):7483-7494. PubMed ID: 36158002
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  • 6. Gitelman Syndrome: A Case Report.
    Rocha J, Pacheco M, Matos M, Ferreira S, Almeida JS.
    Cureus; 2023 May 26; 15(5):e38418. PubMed ID: 37273382
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  • 8. Renal calcium and magnesium handling in Gitelman syndrome.
    Reyes JV, Medina PMB.
    Am J Transl Res; 2022 May 26; 14(1):1-19. PubMed ID: 35173827
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    Parmar MS, Muppidi V, Bashir K.
    ; 2024 01 26. PubMed ID: 29083583
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  • 10. Inherited, not acquired, Gitelman syndrome in a patient with Sjögren's syndrome: importance of genetic testing to distinguish the two forms.
    Mishima E, Mori T, Sohara E, Uchida S, Abe T, Ito S.
    CEN Case Rep; 2017 Nov 26; 6(2):180-184. PubMed ID: 28819721
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  • 11. Concurrent Gitelman Syndrome-like Tubulopathy and Grave's Disease.
    Kumar RK, Srimathy V, Annigeri RA.
    Indian J Nephrol; 2022 Nov 26; 32(3):275-278. PubMed ID: 35814325
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  • 12. Gitelman Syndrome Presenting with Cerebellar Ataxia and Tetany.
    Pandya S, Shah S, Dalal S.
    Indian J Nephrol; 2023 Nov 26; 33(2):144-146. PubMed ID: 37234429
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  • 13. Gitelman syndrome: first report of genetically established diagnosis in Greece.
    Galli-Tsinopoulou A, Patseadou M, Hatzidimitriou A, Kokka P, Emmanouilidou E, Lin SH, Tramma D.
    Hippokratia; 2010 Jan 26; 14(1):42-4. PubMed ID: 20411059
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  • 15. Early diagnosis of Gitelman syndrome in a young child: A case report.
    Wu CY, Tsai MH, Chen CC, Kao CH.
    World J Clin Cases; 2022 Mar 26; 10(9):2844-2850. PubMed ID: 35434103
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  • 16. Gitelman syndrome as a cause of psychomotor retardation in a toddler.
    Skalova S, Neuman D, Lnenicka P, Stekrova J.
    Arab J Nephrol Transplant; 2013 Jan 26; 6(1):37-9. PubMed ID: 23282232
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  • 17. First Diagnosis of Gitelman Syndrome During Pregnancy in an Adolescent Female: A Case Report.
    Zacharis K, Alexakis C, Tsapadikou VK, Anagnostaki I, Charitos T.
    Cureus; 2024 May 26; 16(5):e59644. PubMed ID: 38832152
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  • 18. Inherited salt-losing tubulopathy: An old condition but a new category of tubulopathy.
    Nozu K, Yamamura T, Horinouchi T, Nagano C, Sakakibara N, Ishikura K, Hamada R, Morisada N, Iijima K.
    Pediatr Int; 2020 Apr 26; 62(4):428-437. PubMed ID: 31830341
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  • 19. Pseudo-Gitelman Syndrome Presenting with Hypokalemic Metabolic Alkalosis and Hypocalciuria.
    Lee SH, Lee S, Kim H, Kim GH.
    Electrolyte Blood Press; 2023 Dec 26; 21(2):72-76. PubMed ID: 38152600
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  • 20. Identification of compound mutations of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome exhibiting Bartter syndrome-liked phenotypes.
    Dong B, Chen Y, Liu X, Wang Y, Wang F, Zhao Y, Sun X, Zhao W.
    BMC Nephrol; 2020 Aug 05; 21(1):328. PubMed ID: 32758178
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