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4. Familial infantile myoclonic epilepsy: clinical features in a large kindred with autosomal recessive inheritance. de Falco FA; Majello L; Santangelo R; Stabile M; Bricarelli FD; Zara F Epilepsia; 2001 Dec; 42(12):1541-8. PubMed ID: 11879364 [TBL] [Abstract][Full Text] [Related]
5. Autosomal dominant cortical myoclonus and epilepsy (ADCME) with linkage to chromosome 2p11.1-q12.2. Guerrini R; Parmeggiani L; Marini C; Brovedani P; Bonanni P Adv Neurol; 2005; 95():273-9. PubMed ID: 15508930 [No Abstract] [Full Text] [Related]
6. FAME 3: a novel form of progressive myoclonus and epilepsy. Carr JA; van der Walt PE; Nakayama J; Fu YH; Corfield V; Brink P; Ptacek L Neurology; 2007 Apr; 68(17):1382-9. PubMed ID: 17452583 [TBL] [Abstract][Full Text] [Related]
7. An atypical form of familial myoclonus epilepsy. A case report. Sandyk R S Afr Med J; 1982 Mar; 61(10):366-7. PubMed ID: 6801785 [TBL] [Abstract][Full Text] [Related]
8. [A family with progressive myoclonus epilepsy (author's transl)]. Ammann F; Schweingruber R; Paro M Schweiz Arch Neurol Neurochir Psychiatr; 1978; 123(1):3-15. PubMed ID: 153580 [TBL] [Abstract][Full Text] [Related]
9. Segregation analysis of juvenile myoclonic epilepsy. Greenberg DA; Delgado-Escueta AV; Maldonado HM; Widelitz H Genet Epidemiol; 1988; 5(2):81-94. PubMed ID: 3136050 [TBL] [Abstract][Full Text] [Related]
10. Progressive myoclonus epilepsy: genetic and nosological aspects with special reference to 107 Finnish patients. Norio R; Koskiniemi M Clin Genet; 1979 May; 15(5):382-98. PubMed ID: 109240 [TBL] [Abstract][Full Text] [Related]
11. A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype. Licchetta L; Pippucci T; Bisulli F; Cantalupo G; Magini P; Alvisi L; Baldassari S; Martinelli P; Naldi I; Vanni N; Liguori R; Seri M; Tinuper P Epilepsia; 2013 Jul; 54(7):1298-306. PubMed ID: 23663087 [TBL] [Abstract][Full Text] [Related]
13. Familial benign myoclonus epilepsy of adult onset: a previously unrecognized myoclonic disorder. Okino S J Neurol Sci; 1997 Jan; 145(1):113-8. PubMed ID: 9073039 [TBL] [Abstract][Full Text] [Related]
14. Genetics of myoclonic and myoclonus epilepsies. Minassian BA; Sainz J; Delgado-Escueta AV Clin Neurosci; 1995-1996; 3(4):223-35. PubMed ID: 8891396 [TBL] [Abstract][Full Text] [Related]
15. Familial cortical myoclonic tremor with epilepsy: a single syndromic classification for a group of pedigrees bearing common features. van Rootselaar AF; van Schaik IN; van den Maagdenberg AM; Koelman JH; Callenbach PM; Tijssen MA Mov Disord; 2005 Jun; 20(6):665-73. PubMed ID: 15747356 [TBL] [Abstract][Full Text] [Related]
16. Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6. Weissbecker KA; Durner M; Janz D; Scaramelli A; Sparkes RS; Spence MA Am J Med Genet; 1991 Jan; 38(1):32-6. PubMed ID: 1901452 [TBL] [Abstract][Full Text] [Related]
17. Maternally inherited mitochondrial myopathy and myoclonic epilepsy. Rosing HS; Hopkins LC; Wallace DC; Epstein CM; Weidenheim K Ann Neurol; 1985 Mar; 17(3):228-37. PubMed ID: 3922281 [TBL] [Abstract][Full Text] [Related]
18. Familial cortical myoclonic tremor and epilepsy: Description of a new South African pedigree with 30 year follow up. van Coller R; van Rootselaar AF; Schutte C; van der Meyden CH Parkinsonism Relat Disord; 2017 May; 38():35-40. PubMed ID: 28237853 [TBL] [Abstract][Full Text] [Related]
19. Adult-onset autosomal dominant myoclonic epilepsy: report of a family with an overlooked epileptic syndrome. Hsin YL; Chuang MF; Shyu WC; Lin CY; Chen YH; Harnod T Seizure; 2007 Mar; 16(2):160-5. PubMed ID: 17174115 [TBL] [Abstract][Full Text] [Related]
20. Clinical and genetic analysis of a large pedigree with juvenile myoclonic epilepsy. Serratosa JM; Delgado-Escueta AV; Medina MT; Zhang Q; Iranmanesh R; Sparkes RS Ann Neurol; 1996 Feb; 39(2):187-95. PubMed ID: 8967750 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]