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Gitelman disease associated with growth hormone deficiency, disturbances in vasopressin secretion and empty sella: a new hereditary renal tubular-pituitary syndrome?
Bettinelli A, Rusconi R, Ciarmatori S, Righini V, Zammarchi E, Donati MA, Isimbaldi C, Bevilacqua M, Cesareo L, Tedeschi S, Garavaglia R, Casari G. Bettinelli A, et al. Among authors: ciarmatori s. Pediatr Res. 1999 Aug;46(2):232-8. doi: 10.1203/00006450-199908000-00017. Pediatr Res. 1999. PMID: 10447120
Overlapping functions of the pRb family in the regulation of rRNA synthesis.
Ciarmatori S, Scott PH, Sutcliffe JE, McLees A, Alzuherri HM, Dannenberg JH, te Riele H, Grummt I, Voit R, White RJ. Ciarmatori S, et al. Mol Cell Biol. 2001 Sep;21(17):5806-14. doi: 10.1128/MCB.21.17.5806-5814.2001. Mol Cell Biol. 2001. PMID: 11486020 Free PMC article.
Phenotypic variability in Bartter syndrome type I.
Bettinelli A, Ciarmatori S, Cesareo L, Tedeschi S, Ruffa G, Appiani AC, Rosini A, Grumieri G, Mercuri B, Sacco M, Leozappa G, Binda S, Cecconi M, Navone C, Curcio C, Syren ML, Casari G. Bettinelli A, et al. Among authors: ciarmatori s. Pediatr Nephrol. 2000 Sep;14(10-11):940-5. doi: 10.1007/pl00013418. Pediatr Nephrol. 2000. PMID: 10975303
12 results