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22. [Unverricht's syndrome (familial and hereditary disease of the nervous system)]. CARON S; MICHEL P Laval Med; 1950 Dec; 15(10):1354-64. PubMed ID: 14805166 [No Abstract] [Full Text] [Related]
23. Novel cystatin B mutation and diagnostic PCR assay in an Unverricht-Lundborg progressive myoclonus epilepsy patient. Bespalova IN; Adkins S; Pranzatelli M; Burmeister M Am J Med Genet; 1997 Sep; 74(5):467-71. PubMed ID: 9342192 [TBL] [Abstract][Full Text] [Related]
33. Clinical features and genetics of progressive myoclonus epilepsy of the Univerricht-Lundborg type. Lehesjoki AE; Koskiniemi M Ann Med; 1998 Oct; 30(5):474-80. PubMed ID: 9814834 [TBL] [Abstract][Full Text] [Related]
34. Myoclonic epilepsies of infancy and childhood. Aicardi J Adv Neurol; 1986; 43():11-31. PubMed ID: 3080848 [TBL] [Abstract][Full Text] [Related]
35. Description of a family with a novel progressive myoclonus epilepsy and cognitive impairment. Ferlazzo E; Italiano D; An I; Calarese T; Laguitton V; Bramanti P; Di Bella P; Genton P Mov Disord; 2009 May; 24(7):1016-22. PubMed ID: 19243074 [TBL] [Abstract][Full Text] [Related]
36. [CLINICAL PICTURE AND ELECTROENCEPHALOGRAPHIC PICTURE OF MYOCLONUS EPILEPSY IN TWINS]. HANZAL F; LESNY I Cesk Neurol; 1963 May; 26():192-6. PubMed ID: 14043788 [No Abstract] [Full Text] [Related]
37. 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]