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Long-term follow-up of patients with Bartter syndrome type I and II.
Puricelli E, Bettinelli A, Borsa N, Sironi F, Mattiello C, Tammaro F, Tedeschi S, Bianchetti MG; Italian Collaborative Group for Bartter Syndrome. Puricelli E, et al. Among authors: bettinelli a. Nephrol Dial Transplant. 2010 Sep;25(9):2976-81. doi: 10.1093/ndt/gfq119. Epub 2010 Mar 10. Nephrol Dial Transplant. 2010. PMID: 20219833 Free article.
Early appearance of hypokalemia in Gitelman syndrome.
Tammaro F, Bettinelli A, Cattarelli D, Cavazza A, Colombo C, Syrén ML, Tedeschi S, Bianchetti MG. Tammaro F, et al. Among authors: bettinelli a. Pediatr Nephrol. 2010 Oct;25(10):2179-82. doi: 10.1007/s00467-010-1575-1. Epub 2010 Jun 16. Pediatr Nephrol. 2010. PMID: 20552229
Phosphate homeostasis in Bartter syndrome: a case-control study.
Bettinelli A, Viganò C, Provero MC, Barretta F, Albisetti A, Tedeschi S, Scicchitano B, Bianchetti MG. Bettinelli A, et al. Pediatr Nephrol. 2014 Nov;29(11):2133-8. doi: 10.1007/s00467-014-2846-z. Epub 2014 Jun 6. Pediatr Nephrol. 2014. PMID: 24902942
Urinary exosomes in the diagnosis of Gitelman and Bartter syndromes.
Corbetta S, Raimondo F, Tedeschi S, Syrèn ML, Rebora P, Savoia A, Baldi L, Bettinelli A, Pitto M. Corbetta S, et al. Among authors: bettinelli a. Nephrol Dial Transplant. 2015 Apr;30(4):621-30. doi: 10.1093/ndt/gfu362. Epub 2014 Nov 23. Nephrol Dial Transplant. 2015. PMID: 25422309
The mutation c.1196_1202dup7bp (p.Ser402X) in the SLC12A3 gene clusters in Italian Gitelman syndrome patients and reflects the presence of a common ancestor.
Syrén ML, Borsa Ghiringhelli N, Bettinelli A, Colussi G, Vargas-Poussou R, Tammaro F, Coviello DA, Tedeschi S; Italian Collaborative Group for Gitelman Syndrome. Syrén ML, et al. Among authors: bettinelli a. Nephrol Dial Transplant. 2011 Feb;26(2):557-61. doi: 10.1093/ndt/gfq458. Epub 2010 Jul 30. Nephrol Dial Transplant. 2011. PMID: 20675610
127 results