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SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype.
Motta M, Fasano G, Gredy S, Brinkmann J, Bonnard AA, Simsek-Kiper PO, Gulec EY, Essaddam L, Utine GE, Guarnetti Prandi I, Venditti M, Pantaleoni F, Radio FC, Ciolfi A, Petrini S, Consoli F, Vignal C, Hepbasli D, Ullrich M, de Boer E, Vissers LELM, Gritli S, Rossi C, De Luca A, Ben Becher S, Gelb BD, Dallapiccola B, Lauri A, Chillemi G, Schuh K, Cavé H, Zenker M, Tartaglia M. Motta M, et al. Among authors: gritli s. Am J Hum Genet. 2021 Nov 4;108(11):2112-2129. doi: 10.1016/j.ajhg.2021.09.007. Epub 2021 Oct 8. Am J Hum Genet. 2021. PMID: 34626534 Free PMC article.
Validation of Recombinant Salivary Protein PpSP32 as a Suitable Marker of Human Exposure to Phlebotomus papatasi, the Vector of Leishmania major in Tunisia.
Marzouki S, Kammoun-Rebai W, Bettaieb J, Abdeladhim M, Hadj Kacem S, Abdelkader R, Gritli S, Chemkhi J, Aslan H, Kamhawi S, Ben Salah A, Louzir H, Valenzuela JG, Ben Ahmed M. Marzouki S, et al. Among authors: gritli s. PLoS Negl Trop Dis. 2015 Sep 14;9(9):e0003991. doi: 10.1371/journal.pntd.0003991. eCollection 2015. PLoS Negl Trop Dis. 2015. PMID: 26368935 Free PMC article.
Association of the long QT syndrome With goiter and deafness.
Gritli S, Ben Salah M, Shili A, Robson CD, Ferjaoui M, Hendaoui L, Belhani A, Jilani SB, Gusella JF, Macrae CA. Gritli S, et al. Am J Cardiol. 2010 Mar 1;105(5):681-6. doi: 10.1016/j.amjcard.2009.10.034. Am J Cardiol. 2010. PMID: 20185017
56 results