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Page 1
Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum.
Casali C, Valente EM, Bertini E, Montagna G, Criscuolo C, De Michele G, Villanova M, Damiano M, Pierallini A, Brancati F, Scarano V, Tessa A, Cricchi F, Grieco GS, Muglia M, Carella M, Martini B, Rossi A, Amabile GA, Nappi G, Filla A, Dallapiccola B, Santorelli FM. Casali C, et al. Among authors: dallapiccola b. Neurology. 2004 Jan 27;62(2):262-8. doi: 10.1212/wnl.62.2.262. Neurology. 2004. PMID: 14745065
The epsilon-sarcoglycan gene in myoclonic syndromes.
Valente EM, Edwards MJ, Mir P, DiGiorgio A, Salvi S, Davis M, Russo N, Bozi M, Kim HT, Pennisi G, Quinn N, Dallapiccola B, Bhatia KP. Valente EM, et al. Among authors: dallapiccola b. Neurology. 2005 Feb 22;64(4):737-9. doi: 10.1212/01.WNL.0000151979.68010.9B. Neurology. 2005. PMID: 15728306
The expanding joubert spectrum.
Valente EM, Brancati F, Dallapiccola B. Valente EM, et al. Among authors: dallapiccola b. Neuroradiol J. 2007 Aug 31;20(4):421-5. doi: 10.1177/197140090702000406. Epub 2007 Aug 31. Neuroradiol J. 2007. PMID: 24299702 No abstract available.
Role of the dopamine D5 receptor (DRD5) as a susceptibility gene for cervical dystonia.
Brancati F, Valente EM, Castori M, Vanacore N, Sessa M, Galardi G, Berardelli A, Bentivoglio AR, Defazio G, Girlanda P, Abbruzzese G, Albanese A, Dallapiccola B; Italian Movement Disorder Study Group. Brancati F, et al. Among authors: dallapiccola b. J Neurol Neurosurg Psychiatry. 2003 May;74(5):665-6. doi: 10.1136/jnnp.74.5.665. J Neurol Neurosurg Psychiatry. 2003. PMID: 12700316 Free PMC article.
Ablepharon-macrostomia syndrome in a 46-year-old woman.
Brancati F, Mingarelli R, Sarkozy A, Dallapiccola B. Brancati F, et al. Among authors: dallapiccola b. Am J Med Genet A. 2004 May 15;127A(1):96-98. doi: 10.1002/ajmg.a.20658. Am J Med Genet A. 2004. PMID: 15103726
981 results