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324 results

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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: sacco p. J Child Neurol. 2008 Jun;23(6):683-9. doi: 10.1177/0883073807309778. Epub 2008 Jan 8. J Child Neurol. 2008. PMID: 18182642
18q-syndrome and ectodermal dysplasia syndrome: description of a child and his family.
Zannolli R, Pierluigi M, Pucci L, Lagrasta N, Gasparre O, Matera MR, Di Bartolo RM, Mazzei MA, Sacco P, Miracco C, de Santi MM, Aitiani P, Cavani S, Pellegrini L, Fimiani M, Alessandrini C, Galluzzi P, Livi W, Gonnelli S, Terrosi-Vagnoli P, Zappella M, Morgese G. Zannolli R, et al. Among authors: sacco p. Am J Med Genet A. 2003 Jan 15;116A(2):192-9. doi: 10.1002/ajmg.a.10069. Am J Med Genet A. 2003. PMID: 12494443
Posterior knee pain: primary symptom of a small non-occlusive venous clot.
Zannolli R, Mazzei MA, Sacco P, Turchetti V, Amato T, Battistini S, Berardi R, Volterrani L, De Stefano V, Morgese G. Zannolli R, et al. Among authors: sacco p. Arch Dis Child. 2003 Aug;88(8):728-9; discussion 728-9. doi: 10.1136/adc.88.8.728. Arch Dis Child. 2003. PMID: 12876176 Free PMC article.
Hereditary xanthinuria type II associated with mental delay, autism, cortical renal cysts, nephrocalcinosis, osteopenia, and hair and teeth defects.
Zannolli R, Micheli V, Mazzei MA, Sacco P, Piomboni P, Bruni E, Miracco C, de Santi MM, Terrosi Vagnoli P, Volterrani L, Pellegrini L, Livi W, Lucani B, Gonnelli S, Burlina AB, Jacomelli G, Macucci F, Pucci L, Fimiani M, Swift JA, Zappella M, Morgese G. Zannolli R, et al. Among authors: sacco p. J Med Genet. 2003 Nov;40(11):e121. doi: 10.1136/jmg.40.11.e121. J Med Genet. 2003. PMID: 14627688 Free PMC article. No abstract available.
Hypertelorism, ptosis, and myopia associated with drug-resistant epilepsy, mental delay, growth deficiency, ectodermal defects, and osteopenia.
Zannolli R, Buoni S, Macucci F, Miracco C, de Santi MM, Piomboni P, Bruni E, Malandrini A, Galluzzi P, Hadjistilianou T, Medaglini S, Mazzei MA, Sacco P, Terrosi-Vagnoli P, Volterrani L, Molinelli M, Burlina AB, Swift JA, Fimiani M. Zannolli R, et al. Among authors: sacco p. Am J Med Genet A. 2004 Jun 1;127A(2):212-6. doi: 10.1002/ajmg.a.20692. Am J Med Genet A. 2004. PMID: 15108215
Global developmental delay, osteopenia and ectodermal defect: a new syndrome.
Zannolli R, Buoni S, Macucci F, Santi MM, Miracco F, Pierluigi M, Mogni M, Piomboni P, Massafra MR, Galluzzi P, Livi W, Cuccia A, Margollicci MA, Pucci L, Sacco P, Molinelli M, Burlina AB, Swift JA, Fimiani M, Zappella M, Miracco C. Zannolli R, et al. Among authors: sacco p. Brain Dev. 2006 Apr;28(3):155-61. doi: 10.1016/j.braindev.2005.06.011. Epub 2005 Dec 20. Brain Dev. 2006. PMID: 16368207
Follow-up of endovascular aortic aneurysm repair: Preliminary validation of digital tomosynthesis and contrast enhanced ultrasound in detection of medium- to long-term complications.
Mazzei MA, Guerrini S, Mazzei FG, Cioffi Squitieri N, Notaro D, de Donato G, Galzerano G, Sacco P, Setacci F, Volterrani L, Setacci C. Mazzei MA, et al. Among authors: sacco p. World J Radiol. 2016 May 28;8(5):530-6. doi: 10.4329/wjr.v8.i5.530. World J Radiol. 2016. PMID: 27247719 Free PMC article.
324 results