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Page 1
Electroretinographic findings in inherited ataxias.
Palma V, Ambrosio G, De Michele G, Mansi D, Trombetta L, Brescia Morra V, Filla A. Palma V, et al. Among authors: ambrosio g. Acta Neurol (Napoli). 1989 Dec;11(6):383-9. Acta Neurol (Napoli). 1989. PMID: 2618824
Cerebellar vermis hypoplasia in a case of cri-du-chat syndrome.
De Michele G, Presta M, Di Salle F, Serra L, Mazzaccara A, Della Rocca G, Ambrosio G, Filla A. De Michele G, et al. Among authors: ambrosio g. Acta Neurol (Napoli). 1993 Apr;15(2):92-6. Acta Neurol (Napoli). 1993. PMID: 8328329
A genetic study of Parkinson's disease.
De Michele G, Filla A, Marconi R, Volpe G, D'Alessio A, Scala R, Ambrosio G, Campanella G. De Michele G, et al. Among authors: ambrosio g. J Neural Transm Suppl. 1995;45:21-5. J Neural Transm Suppl. 1995. PMID: 8748605
The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
Bonifati V, De Michele G, Lücking CB, Dürr A, Fabrizio E, Ambrosio G, Vanacore N, De Mari M, Marconi R, Capus L, Breteler MM, Gasser T, Oostra B, Wood N, Agid Y, Filla A, Meco G, Brice A; Italian PD Genetics Study Group, French PD Genetics Study Group, European Consortium on Genetic Susceptibility in PD. Bonifati V, et al. Among authors: ambrosio g. Neurol Sci. 2001 Feb;22(1):51-2. doi: 10.1007/s100720170042. Neurol Sci. 2001. PMID: 11487197
Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus.
Muglia M, Criscuolo C, Magariello A, De Michele G, Scarano V, D'Adamo P, Ambrosio G, Gabriele AL, Patitucci A, Mazzei R, Conforti FL, Sprovieri T, Morgante L, Epifanio A, La Spina P, Valentino P, Gasparini P, Filla A, Quattrone A. Muglia M, et al. Among authors: ambrosio g. Neurogenetics. 2004 Feb;5(1):49-54. doi: 10.1007/s10048-003-0167-7. Epub 2003 Dec 5. Neurogenetics. 2004. PMID: 14658060
989 results