Amabile GA - Search Results

1

Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish family.

Casali C, Bonifati V, Santorelli FM, Casari G, Fortini D, Patrignani A, Fabbrini G, Carrozzo R, D'Amati G, Locuratolo N, Vanacore N, Damiano M, Pierallini A, Pierelli F, Amabile GA, Meco G. Casali C, et al. Among authors: amabile ga. Neurology. 2001 Mar 27;56(6):802-5. doi: 10.1212/wnl.56.6.802. Neurology. 2001. PMID: 11274324

2

Multiple mtDNA deletions: clinical and molecular correlations.

Santorelli FM, De Joanna G, Casali C, Tessa A, Siciliano G, Amabile GA, Pierelli F, Vilarinho L, Santoro L. Santorelli FM, et al. Among authors: amabile ga. J Inherit Metab Dis. 2000 Mar;23(2):155-61. doi: 10.1023/a:1005617916260. J Inherit Metab Dis. 2000. PMID: 10801057

3

SPG3A: An additional family carrying a new atlastin mutation.

Tessa A, Casali C, Damiano M, Bruno C, Fortini D, Patrono C, Cricchi F, Valoppi M, Nappi G, Amabile GA, Bertini E, Santorelli FM. Tessa A, et al. Among authors: amabile ga. Neurology. 2002 Dec 24;59(12):2002-5. doi: 10.1212/01.wnl.0000036902.21438.98. Neurology. 2002. PMID: 12499504

4

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: amabile ga. Neurology. 2004 Jan 27;62(2):262-8. doi: 10.1212/wnl.62.2.262. Neurology. 2004. PMID: 14745065

5

Current insights into familial spastic paraparesis: new advances in an old disease.

Fortini D, Cricchi F, Di Fabio R, Damiano M, Comanducci G, Benedetti L, Valoppi M, Grieco GS, D'Eugenio O, Celato A, Santorelli F, Casali C, Amabile GA, Pierelli F. Fortini D, et al. Among authors: amabile ga. Funct Neurol. 2003 Jan-Mar;18(1):43-9. Funct Neurol. 2003. PMID: 12760414 Review.

6

Intrafamilial variability in hereditary spastic paraplegia associated with an SPG4 gene mutation.

Santorelli FM, Patrono C, Fortini D, Tessa A, Comanducci G, Bertini E, Pierallini A, Amabile GA, Casali C. Santorelli FM, et al. Among authors: amabile ga. Neurology. 2000 Sep 12;55(5):702-5. doi: 10.1212/wnl.55.5.702. Neurology. 2000. PMID: 10980739

7

Pilomotor epilepsy.

Scoppetta C, Casali C, D'Agostini S, Amabile G, Morocutti C. Scoppetta C, et al. Funct Neurol. 1989 Jul-Sep;4(3):283-6. Funct Neurol. 1989. PMID: 2676747 Review.

8

Early diagnosis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): the role of MRI.

Fattapposta F, Restuccia R, Pirro C, Malandrini A, Locuratolo N, Amabile G, Bianco F. Fattapposta F, et al. Funct Neurol. 2004 Oct-Dec;19(4):239-42. Funct Neurol. 2004. PMID: 15776792

9

Respiratory chain defects in hereditary spastic paraplegias.

Piemonte F, Casali C, Carrozzo R, Schägger H, Patrono C, Tessa A, Tozzi G, Cricchi F, Di Capua M, Siciliano G, Amabile GA, Morocutti C, Bertini E, Santorelli FM. Piemonte F, et al. Among authors: amabile ga. Neuromuscul Disord. 2001 Sep;11(6-7):565-9. doi: 10.1016/s0960-8966(01)00214-0. Neuromuscul Disord. 2001. PMID: 11525886

10

Event-related potentials and autonomic functions.

Morocutti C, Fattapposta F, Pierelli F, Cordischi MV, Della Rocca M, Amabile G. Morocutti C, et al. Funct Neurol. 1987 Oct-Dec;2(4):517-21. Funct Neurol. 1987. PMID: 3443376

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