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Page 1
Polydactyly with ectodermal defect, osteopenia, and mental delay.
Zannolli R, Buoni S, Viviano M, Macucci F, D'Ambrosio A, Livi W, Mazzei MA, Mazzei F, Sacco P, Volterrani L, Vonella G, Orsi A, Zappella M, Hayek J. Zannolli R, et al. Among authors: vonella g. J Child Neurol. 2008 Jun;23(6):683-9. doi: 10.1177/0883073807309778. Epub 2008 Jan 8. J Child Neurol. 2008. PMID: 18182642
MECP2 deletions and genotype-phenotype correlation in Rett syndrome.
Scala E, Longo I, Ottimo F, Speciale C, Sampieri K, Katzaki E, Artuso R, Mencarelli MA, D'Ambrogio T, Vonella G, Zappella M, Hayek G, Battaglia A, Mari F, Renieri A, Ariani F. Scala E, et al. Among authors: vonella g. Am J Med Genet A. 2007 Dec 1;143A(23):2775-84. doi: 10.1002/ajmg.a.32002. Am J Med Genet A. 2007. PMID: 17968969
Long-term plasma levels of leptin and adiponectin in Rett syndrome.
Blardi P, de Lalla A, D'Ambrogio T, Vonella G, Ceccatelli L, Auteri A, Hayek J. Blardi P, et al. Among authors: vonella g. Clin Endocrinol (Oxf). 2009 May;70(5):706-9. doi: 10.1111/j.1365-2265.2008.03386.x. Epub 2008 Aug 15. Clin Endocrinol (Oxf). 2009. PMID: 18710461