Carrozzo R - Search Results

1

Locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16.

Guerrini R, Parmeggiani L, Bonanni P, Carrozzo R, Casari G. Guerrini R, et al. Among authors: carrozzo r. Neurology. 2000 Sep 12;55(5):738-9. doi: 10.1212/wnl.55.5.735-c. Neurology. 2000. PMID: 10980756 No abstract available.

2

Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2.

Guerrini R, Bonanni P, Nardocci N, Parmeggiani L, Piccirilli M, De Fusco M, Aridon P, Ballabio A, Carrozzo R, Casari G. Guerrini R, et al. Among authors: carrozzo r. Ann Neurol. 1999 Mar;45(3):344-52. doi: 10.1002/1531-8249(199903)45:3<344::aid-ana10>3.0.co;2-9. Ann Neurol. 1999. PMID: 10072049

3

Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures: A newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2.

Guerrini R, Bonanni P, Patrignani A, Brown P, Parmeggiani L, Grosse P, Brovedani P, Moro F, Aridon P, Carrozzo R, Casari G. Guerrini R, et al. Among authors: carrozzo r. Brain. 2001 Dec;124(Pt 12):2459-75. doi: 10.1093/brain/124.12.2459. Brain. 2001. PMID: 11701600

4

A nonsense mutation of the ATRX gene causing mild mental retardation and epilepsy.

Guerrini R, Shanahan JL, Carrozzo R, Bonanni P, Higgs DR, Gibbons RJ. Guerrini R, et al. Among authors: carrozzo r. Ann Neurol. 2000 Jan;47(1):117-21. Ann Neurol. 2000. PMID: 10632111

5

Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene.

Moro F, Carrozzo R, Veggiotti P, Tortorella G, Toniolo D, Volzone A, Guerrini R. Moro F, et al. Among authors: carrozzo r. Neurology. 2002 Mar 26;58(6):916-21. doi: 10.1212/wnl.58.6.916. Neurology. 2002. PMID: 11914408

6

Nonsyndromic mental retardation and cryptogenic epilepsy in women with doublecortin gene mutations.

Guerrini R, Moro F, Andermann E, Hughes E, D'Agostino D, Carrozzo R, Bernasconi A, Flinter F, Parmeggiani L, Volzone A, Parrini E, Mei D, Jarosz JM, Morris RG, Pratt P, Tortorella G, Dubeau F, Andermann F, Dobyns WB, Das S. Guerrini R, et al. Among authors: carrozzo r. Ann Neurol. 2003 Jul;54(1):30-7. doi: 10.1002/ana.10588. Ann Neurol. 2003. PMID: 12838518

7

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: carrozzo r. Neurology. 2001 Mar 27;56(6):802-5. doi: 10.1212/wnl.56.6.802. Neurology. 2001. PMID: 11274324

8

Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing.

Guerrini R, Carrozzo R. Guerrini R, et al. Among authors: carrozzo r. Seizure. 2001 Oct;10(7):532-43; quiz 544-7. doi: 10.1053/seiz.2001.0650. Seizure. 2001. PMID: 11749114 Free article. Review.

9

Bilateral perisylvian polymicrogyria in three generations.

Borgatti R, Triulzi F, Zucca C, Piccinelli P, Balottin U, Carrozzo R, Guerrini R. Borgatti R, et al. Among authors: carrozzo r. Neurology. 1999 Jun 10;52(9):1910-3. doi: 10.1212/wnl.52.9.1910. Neurology. 1999. PMID: 10371547

10

Angelman syndrome: etiology, clinical features, diagnosis, and management of symptoms.

Guerrini R, Carrozzo R, Rinaldi R, Bonanni P. Guerrini R, et al. Among authors: carrozzo r. Paediatr Drugs. 2003;5(10):647-61. doi: 10.2165/00148581-200305100-00001. Paediatr Drugs. 2003. PMID: 14510623 Review.

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