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References

  • Chen R, Cros D, Curra A, Di Lazzaro V, Lefaucheur JP, Magistris MR, Mills K, Rösler KM, Triggs WJ, Ugawa Y, Ziemann U. (2008) The clinical diagnostic utility of transcranial magnetic stimulation: report of an IFCN committee. Clin Neurophysiol 119:504532.
  • Cottingham RW Jr, Idury RM, Schaffer AA. (1993) Faster sequential genetic linkage computations. Am J Hum Genet 53:252263.
  • De Falco FA, Striano P, De Falco A, Striano S, Santangelo R, Perretti A, Balbi P, Lecconi M, Zara F. (2003) Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME. Neurology 60:13811385.
  • Guerrini R, Bonanni P, Patrignani A, Brown P, Parmeggiani L, Grosse P, Brovedani P, Moro F, Aridon P, Carrozzo R, Casari G. (2001) 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. Brain 124:24592475.
  • Madia F, Striano P, Di Bonaventura C, De Falco A, De Falco FA, Manfredi M, Casari G, Striano S, Minetti C, Zara F. (2008) Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families. Neurogenetics 9:139142.
  • Mikami M, Yasuda T, Terao A, Nakamura M, Ueno S, Tanabe H, Tanaka T, Onuma T, Goto Y, Kaneko S, Sano A. (1999) Localization of a gene for benign adult familial myoclonic epilepsy to chromosome 8q23.3-q24.1. Am J Hum Genet 65:745751.
  • Plaster NM, Uyama E, Uchino M, Ikeda T, Flanigan KM, Kondo I, Ptacek LJ. (1999) Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24. Neurology 53:11801183.
  • Van Rootselaar AF, Van Schaik IN, Van Den Maagdenberg AMJM, Koelman JHTM, Callenbach PM, Tijssen MA. (2005) Familial cortical myoclonic tremor with epilepsy: a single syndromic classification for a group of pedigrees bearing common features. Mov Disord 20:665673.
  • Van Rootselaar AF, Van Der Salm SM, Bour LJ, Edwards MJ, Brown P, Aronica E, Rozemuller-Kwakkel JM, Koehler PJ, Koelman JH, Rothwell JC, Tijssen MA. (2007) Decreased cortical inhibition and yet cerebellar pathology in “familial cortical myoclonic tremor with epilepsy. Mov Disord 22:23782385.
  • Striano P, Chifari R, Striano S, De Fusco M, Elia M, Guerrini R, Casari G, Canevini MP. (2004) A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2. Epilepsia 45:190192.
  • Striano P, Zara F, Striano S. (2005) Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype (Review). Acta Neurol Scand 111:211217.