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Journal Abstract Search

229 related items for PubMed ID: 29083583

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  • 5. 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; 62(4):428-437. PubMed ID: 31830341
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  • 6. 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; 6(1):37-9. PubMed ID: 23282232
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  • 7. Renal calcium and magnesium handling in Gitelman syndrome.
    Reyes JV, Medina PMB.
    Am J Transl Res; 2022 Jan; 14(1):1-19. PubMed ID: 35173827
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  • 8. Clinical and Genetic Features in 31 Serial Chinese Children With Gitelman Syndrome.
    Zhang L, Huang K, Wang S, Fu H, Wang J, Shen H, Lu Z, Chen J, Bao Y, Feng C, Dong G, Mao J.
    Front Pediatr; 2021 Jan; 9():544925. PubMed ID: 33996672
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  • 9. Unmasking of Gitelman Syndrome during Pregnancy in an Adolescent with Thyrotoxic Crisis.
    Acharya R, Upadhyay K.
    Pediatr Rep; 2021 Dec 01; 13(4):632-638. PubMed ID: 34941636
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  • 10. Cardiac Arrest as the First Presentation of Gitelman Syndrome.
    Geletu A, Gardner-Gray J, Roche M, Ngassa M.
    Cureus; 2023 Jan 01; 15(1):e33565. PubMed ID: 36779094
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  • 11. Gitelman Syndrome Presenting with Cerebellar Ataxia and Tetany.
    Pandya S, Shah S, Dalal S.
    Indian J Nephrol; 2023 Jan 01; 33(2):144-146. PubMed ID: 37234429
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  • 12. Mutations in SLC12A3 and CLCNKB and Their Correlation with Clinical Phenotype in Patients with Gitelman and Gitelman-like Syndrome.
    Lee JW, Lee J, Heo NJ, Cheong HI, Han JS.
    J Korean Med Sci; 2016 Jan 01; 31(1):47-54. PubMed ID: 26770037
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  • 13. Gitelman Syndrome: A Rare Cause of Seizure Disorder and a Systematic Review.
    Shahzad MA, Mukhtar M, Ahmed A, Ullah W, Saeed R, Hamid M.
    Case Rep Med; 2019 Jan 01; 2019():4204907. PubMed ID: 30867665
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  • 14. Gitelman Syndrome: A Case Report.
    Rocha J, Pacheco M, Matos M, Ferreira S, Almeida JS.
    Cureus; 2023 May 01; 15(5):e38418. PubMed ID: 37273382
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  • 15. Case report: Gitelman syndrome with diabetes: Confirmed by both hydrochlorothiazide test and genetic testing.
    Yang L, Fan J, Liu Y, Ren Y, Liu Z, Fu H, Qi H, Yang J.
    Medicine (Baltimore); 2023 Jun 16; 102(24):e33959. PubMed ID: 37327293
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  • 16. [Bartter-Gitelman syndromes].
    Blanchard A, Courand PY, Livrozet M, Vargas-Poussou R.
    Nephrol Ther; 2020 Jul 16; 16(4):233-243. PubMed ID: 32622651
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  • 17. Heart's Dangerous Symphony: Torsade De Pointes Unleashed by Gitelman Syndrome-Induced Hypomagnesemia.
    Idries IY, Azhar M, Yadav R, Nevolina A, Ullah A, Sur A, Zadoretska I, Gunsburg M.
    Cureus; 2023 Aug 16; 15(8):e44464. PubMed ID: 37791211
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  • 18. 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 16; 6(2):180-184. PubMed ID: 28819721
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  • 19. The Impact of Gitelman Syndrome on Cardiovascular Disease: From Physiopathology to Clinical Management.
    Bezzeccheri A, Di Giovanni G, Belli M, Mollace R, Barone L, Macrini M, Di Landro A, Muscoli S.
    Rev Cardiovasc Med; 2022 Aug 16; 23(8):289. PubMed ID: 39076641
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  • 20. Gitelman syndrome associated with chondrocalcinosis and severe neuropathy: a novel heterozygous mutation in SLC12A3 gene.
    Conticini E, Negro A, Magnani L, Ugolini R, Atienza-Mateo B, Frediani B, Salvarani C.
    Reumatismo; 2020 Apr 10; 72(1):67-70. PubMed ID: 32292023
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