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70 results

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Page 1
Gene symbol: MECP2. Disease: Rett syndrome.
Conforti FL, Mazzei R, Patitucci A, Magariello A, Sprovieri T, Ungaro C, Gabriele AL, Muglia M, Del Giudice E, Quattrone A. Conforti FL, et al. Among authors: ungaro c. Hum Genet. 2006 Jul;119(6):675. Hum Genet. 2006. PMID: 17128467 No abstract available.
Gene symbol: MECP2. Disease: Rett syndrome.
Conforti FL, Mazzei R, Sprovieri T, Ungaro C, Patitucci A, Magariello A, Gabriele AL, Bravaccio C, Muglia M, Quattrone A. Conforti FL, et al. Among authors: ungaro c. Hum Genet. 2006 Jul;119(6):676. Hum Genet. 2006. PMID: 17128468 No abstract available.
Gene symbol: NOTCH3.
Mazzei R, Conforti FL, Ungaro C, Liguori M, Sprovieri T, Patitucci A, Magariello A, Gabriele AL, Muglia M, Quattrone A. Mazzei R, et al. Among authors: ungaro c. Hum Genet. 2007 Apr;121(2):295. Hum Genet. 2007. PMID: 17598216 No abstract available.
Gene symbol: NOTCH3.
Mazzei R, Conforti FL, Ungaro C, Liguori M, Magariello A, Gabriele AL, Patitucci A, Sprovieri T, Muglia M, Quattrone A. Mazzei R, et al. Among authors: ungaro c. Hum Genet. 2007 Apr;121(2):296. Hum Genet. 2007. PMID: 17598243 No abstract available.
Gene symbol: NOTCH3.
Mazzei R, Conforti FL, Ungaro C, Liguori M, Sprovieri T, Patitucci A, Magariello A, Gabriele AL, Muglia M, Quattrone A. Mazzei R, et al. Among authors: ungaro c. Hum Genet. 2007 Apr;121(2):296. Hum Genet. 2007. PMID: 17598244 No abstract available.
Gene symbol: NOTCH3. Disease: CADASIL.
Ungaro C, Sprovieri T, Conforti FL, Consoli D, Citrigno L, Liguori M, Quattrone A, Mazzei R. Ungaro C, et al. Hum Genet. 2008 Jun;123(5):554. Hum Genet. 2008. PMID: 20960662 No abstract available.
Gene symbol: NOTCH3. Disease: CADASIL.
Ungaro C, Conforti FL, Sprovieri T, de Robertis F, Citrigno L, Quattrone A, Mazzei R. Ungaro C, et al. Hum Genet. 2008 Jun;123(5):555. Hum Genet. 2008. PMID: 20960663 No abstract available.
Gene symbol: MECP2. Disease: Rett syndrome.
Sprovieri T, Mazzei R, Ungaro C, Citrigno L, Quattrone A, Conforti FL. Sprovieri T, et al. Among authors: ungaro c. Hum Genet. 2008 Jun;123(5):555. Hum Genet. 2008. PMID: 20960664 No abstract available.
A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy.
Conforti FL, Sprovieri T, Mazzei R, Ungaro C, La Bella V, Tessitore A, Patitucci A, Magariello A, Gabriele AL, Tedeschi G, Simone IL, Majorana G, Valentino P, Condino F, Bono F, Monsurrò MR, Muglia M, Quattrone A. Conforti FL, et al. Among authors: ungaro c. Neuromuscul Disord. 2008 Jan;18(1):68-70. doi: 10.1016/j.nmd.2007.07.003. Epub 2007 Aug 20. Neuromuscul Disord. 2008. PMID: 17703939
70 results