Nappi G - Search Results

1

Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 gene.

Siciliano G, Tessa A, Petrini S, Mancuso M, Bruno C, Grieco GS, Malandrini A, DeFlorio L, Martini B, Federico A, Nappi G, Santorelli FM, Murri L. Siciliano G, et al. Among authors: nappi g. Neuromuscul Disord. 2003 Feb;13(2):162-5. doi: 10.1016/s0960-8966(02)00221-3. Neuromuscul Disord. 2003. PMID: 12565915

2

Migraine-like disorder segregating with mtDNA 14484 Leber hereditary optic neuropathy mutation.

Cupini LM, Massa R, Floris R, Manenti G, Martini B, Tessa A, Nappi G, Bernardi G, Santorelli FM. Cupini LM, et al. Among authors: nappi g. Neurology. 2003 Feb 25;60(4):717-9. doi: 10.1212/01.wnl.0000048662.77572.fb. Neurology. 2003. PMID: 12601121

3

Heterogeneity in migraine: many genes for many phenotypes?

Martini B, Grieco GS, Fortini D, Costa A, Nappi G, Santorelli FM. Martini B, et al. Among authors: nappi g. Funct Neurol. 2001;16(4 Suppl):63-7. Funct Neurol. 2001. PMID: 11996532 Review. No abstract available.

4

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: nappi g. Neurology. 2002 Dec 24;59(12):2002-5. doi: 10.1212/01.wnl.0000036902.21438.98. Neurology. 2002. PMID: 12499504

5

Familial basilar migraine associated with a new mutation in the ATP1A2 gene.

Ambrosini A, D'Onofrio M, Grieco GS, Di Mambro A, Montagna G, Fortini D, Nicoletti F, Nappi G, Sances G, Schoenen J, Buzzi MG, Santorelli FM, Pierelli F. Ambrosini A, et al. Among authors: nappi g. Neurology. 2005 Dec 13;65(11):1826-8. doi: 10.1212/01.wnl.0000187072.71931.c0. Neurology. 2005. PMID: 16344534

6

Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop.

Cricchi F, Di Lorenzo C, Grieco GS, Rengo C, Cardinale A, Racaniello M, Santorelli FM, Nappi G, Pierelli F, Casali C. Cricchi F, et al. Among authors: nappi g. J Neurol Sci. 2007 Mar 15;254(1-2):69-71. doi: 10.1016/j.jns.2007.01.008. Epub 2007 Feb 12. J Neurol Sci. 2007. PMID: 17292920

7

mtDNA A3243G MELAS mutation is not associated with multigenerational female migraine.

Buzzi MG, Di Gennaro G, D'Onofrio M, Ciccarelli O, Santorelli FM, Fortini D, Nappi G, Nicoletti F, Casali C. Buzzi MG, et al. Among authors: nappi g. Neurology. 2000 Feb 22;54(4):1005-7. doi: 10.1212/wnl.54.4.1005. Neurology. 2000. PMID: 10691007

8

Migraine as a complex disease: heterogeneity, comorbidity and genotype-phenotype interactions.

Nappi G, Costa A, Tassorelli C, Santorelli FM. Nappi G, et al. Funct Neurol. 2000 Apr-Jun;15(2):87-93. Funct Neurol. 2000. PMID: 10916720 Review.

9

Retinal migraine as unusual feature of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Ravaglia S, Costa A, Santorelli FM, Nappi G, Moglia A. Ravaglia S, et al. Among authors: nappi g. Cephalalgia. 2004 Jan;24(1):74-7. doi: 10.1111/j.1468-2982.2004.00604.x. Cephalalgia. 2004. PMID: 14687018 No abstract available.

10

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

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