Zara F - Search Results

1

Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity.

Malacarne M, Gennaro E, Madia F, Pozzi S, Vacca D, Barone B, dalla Bernardina B, Bianchi A, Bonanni P, De Marco P, Gambardella A, Giordano L, Lispi ML, Romeo A, Santorum E, Vanadia F, Vecchi M, Veggiotti P, Vigevano F, Viri F, Bricarelli FD, Zara F. Malacarne M, et al. Among authors: zara f. Am J Hum Genet. 2001 Jun;68(6):1521-6. doi: 10.1086/320596. Epub 2001 Apr 20. Am J Hum Genet. 2001. PMID: 11326335 Free PMC article.

2

Mapping of genes predisposing to idiopathic generalized epilepsy.

Zara F, Bianchi A, Avanzini G, Di Donato S, Castellotti B, Patel PI, Pandolfo M. Zara F, et al. Hum Mol Genet. 1995 Jul;4(7):1201-7. doi: 10.1093/hmg/4.7.1201. Hum Mol Genet. 1995. PMID: 8528209

3

Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy.

Minetti C, Sotgia F, Bruno C, Scartezzini P, Broda P, Bado M, Masetti E, Mazzocco M, Egeo A, Donati MA, Volonte D, Galbiati F, Cordone G, Bricarelli FD, Lisanti MP, Zara F. Minetti C, et al. Among authors: zara f. Nat Genet. 1998 Apr;18(4):365-8. doi: 10.1038/ng0498-365. Nat Genet. 1998. PMID: 9537420

4

Unusual EEG pattern linked to chromosome 3p in a family with idiopathic generalized epilepsy.

Zara F, Labuda M, Garofalo PG, Durisotti C, Bianchi A, Castellotti B, Patel PI, Avanzini G, Pandolfo M. Zara F, et al. Neurology. 1998 Aug;51(2):493-8. doi: 10.1212/wnl.51.2.493. Neurology. 1998. PMID: 9710024

5

Benign infantile familial convulsions: natural history of a case and clinical characteristics of a large Italian family.

Giordano L, Accorsi P, Valseriati D, Tiberti A, Menegati E, Zara F, Vignoli A, Vigevano F. Giordano L, et al. Among authors: zara f. Neuropediatrics. 1999 Apr;30(2):99-101. doi: 10.1055/s-2007-973469. Neuropediatrics. 1999. PMID: 10401694

6

No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1.

Gennaro E, Malacarne M, Carbone I, Riggio MC, Bianchi A, Bonanni P, Boniver C, Dalla Bernardina B, De Marco P, Giordano L, Guerrini R, Santorum E, Sebastianelli R, Vecchi M, Veggiotti P, Vigevano F, Bricarelli FD, Zara F. Gennaro E, et al. Among authors: zara f. Epilepsia. 1999 Dec;40(12):1799-803. doi: 10.1111/j.1528-1157.1999.tb01601.x. Epilepsia. 1999. PMID: 10612347 Free article.

7

Mapping of a locus for a familial autosomal recessive idiopathic myoclonic epilepsy of infancy to chromosome 16p13.

Zara F, Gennaro E, Stabile M, Carbone I, Malacarne M, Majello L, Santangelo R, de Falco FA, Bricarelli FD. Zara F, et al. Am J Hum Genet. 2000 May;66(5):1552-7. doi: 10.1086/302876. Epub 2000 Mar 30. Am J Hum Genet. 2000. PMID: 10741954 Free PMC article.

8

Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemia.

Carbone I, Bruno C, Sotgia F, Bado M, Broda P, Masetti E, Panella A, Zara F, Bricarelli FD, Cordone G, Lisanti MP, Minetti C. Carbone I, et al. Among authors: zara f. Neurology. 2000 Mar 28;54(6):1373-6. doi: 10.1212/wnl.54.6.1373. Neurology. 2000. PMID: 10746614

9

Genome search for susceptibility loci of common idiopathic generalised epilepsies.

Sander T, Schulz H, Saar K, Gennaro E, Riggio MC, Bianchi A, Zara F, Luna D, Bulteau C, Kaminska A, Ville D, Cieuta C, Picard F, Prud'homme JF, Bate L, Sundquist A, Gardiner RM, Janssen GA, de Haan GJ, Kasteleijn-Nolst-Trenité DG, Bader A, Lindhout D, Riess O, Wienker TF, Janz D, Reis A. Sander T, et al. Among authors: zara f. Hum Mol Genet. 2000 Jun 12;9(10):1465-72. doi: 10.1093/hmg/9.10.1465. Hum Mol Genet. 2000. PMID: 10888596

10

The first three mosaic cri du chat syndrome patients with two rearranged cell lines.

Perfumo C, Cerruti Mainardi P, Calí A, Coucourde G, Zara F, Cavani S, Overhauser J, Bricarelli FD, Pierluigi M. Perfumo C, et al. Among authors: zara f. J Med Genet. 2000 Dec;37(12):967-72. doi: 10.1136/jmg.37.12.967. J Med Genet. 2000. PMID: 11186943 Free PMC article. No abstract available.

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