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Genetic variant of C1GalT1 contributes to the susceptibility to IgA nephropathy.
Pirulli D, Crovella S, Ulivi S, Zadro C, Bertok S, Rendine S, Scolari F, Foramitti M, Ravani P, Roccatello D, Savoldi S, Cerullo G, Lanzilotta SG, Bisceglia L, Zelante L, Floege J, Alexopoulos E, Kirmizis D, Ghiggeri GM, Frascà G, Schena FP, Amoroso A; European IgAN Consortium. Pirulli D, et al. Among authors: zadro c. J Nephrol. 2009 Jan-Feb;22(1):152-9. J Nephrol. 2009. PMID: 19229831
Are MYO1C and MYO1F associated with hearing loss?
Zadro C, Alemanno MS, Bellacchio E, Ficarella R, Donaudy F, Melchionda S, Zelante L, Rabionet R, Hilgert N, Estivill X, Van Camp G, Gasparini P, Carella M. Zadro C, et al. Biochim Biophys Acta. 2009 Jan;1792(1):27-32. doi: 10.1016/j.bbadis.2008.10.017. Epub 2008 Nov 5. Biochim Biophys Acta. 2009. PMID: 19027848 Free article.
Lactase non-persistent genotype distribution in Italy.
Zadro C, Dipresa S, Zorzetti G, Pediroda A, Menegoni F. Zadro C, et al. Minerva Gastroenterol Dietol. 2017 Sep;63(3):264-269. doi: 10.23736/S1121-421X.16.02355-2. Minerva Gastroenterol Dietol. 2017. PMID: 28673071
Five new OTOF gene mutations and auditory neuropathy.
Zadro C, Ciorba A, Fabris A, Morgutti M, Trevisi P, Gasparini P, Martini A. Zadro C, et al. Int J Pediatr Otorhinolaryngol. 2010 May;74(5):494-8. doi: 10.1016/j.ijporl.2010.02.004. Epub 2010 Mar 7. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20211493
[Neurological trouble in a 68-year-old woman].
Larrauffie A, Porcheron M, Pariente J, Wolfrum M, Bureau C, Zadro C, Otal P, Broue P, Sailler L, Moulis G, Maquet J, Goulabchand R. Larrauffie A, et al. Among authors: zadro c. Rev Med Interne. 2023 Sep;44(9):529-532. doi: 10.1016/j.revmed.2023.05.011. Epub 2023 Jun 7. Rev Med Interne. 2023. PMID: 37296033 French. No abstract available.
16 results