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2. [Hereditary Unverricht-Lundborg myoclonus epilepsy in Congolese Negroes]. JANSSEN P Ann Soc Belg Med Trop (1920); 1954 Jan; 34(1):113-9. PubMed ID: 13181234 [No Abstract] [Full Text] [Related]
3. A clinical analysis of myoclonus epilepsy (Unverricht-Lundborg), myoclonic cerebellar dyssynergy (Hunt) and hepatolenticular degeneration (Wilson). WOHLFART G; HOOK O Acta Psychiatr Neurol Scand; 1951; 26(2):219-45. PubMed ID: 14902532 [No Abstract] [Full Text] [Related]
4. [The relationship of dyssynergia cerebellaris myoclonica (Hunt) to myoclonus epilepsy (Unverricht-Lundborg)]. SEITZ D Dtsch Z Nervenheilkd; 1955; 173(2):111-22. PubMed ID: 14391125 [No Abstract] [Full Text] [Related]
5. [MYOCLONIC EPILEPSY OF THE UNVERRICHT-LUNDBORG TYPE. CLINICAL, ELECTROENCEPHALOGRAPHIC AND ELECTROMYOGRAPHIC STUDY OF A CASE]. MARTINO P; BERT J; ZWINGELSTEIN J; COLLOMB H Bull Soc Med Afr Noire Lang Fr; 1964; 9():181-6. PubMed ID: 14276620 [No Abstract] [Full Text] [Related]
6. [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]
8. 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]
10. Progressive myoclonic ataxia without ragged red fibres: Unverricht-Lundborg disease vs Ramsay Hunt syndrome. Shakir RA; Khan RA; al-Zuhair AG Acta Neurol Scand; 1992 Nov; 86(5):470-3. PubMed ID: 1336290 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Lack of activation of human secondary somatosensory cortex in Unverricht-Lundborg type of progressive myoclonus epilepsy. Forss N; Silén T; Karjalainen T Ann Neurol; 2001 Jan; 49(1):90-7. PubMed ID: 11198301 [TBL] [Abstract][Full Text] [Related]
13. Linkage studies in progressive myoclonus epilepsy: Unverricht-Lundborg and Lafora's diseases. Lehesjoki AE; Koskiniemi M; Pandolfo M; Antonelli A; Kyllerman M; Wahlström J; Nergårdh A; Burmeister M; Sistonen P; Norio R Neurology; 1992 Aug; 42(8):1545-50. PubMed ID: 1641151 [TBL] [Abstract][Full Text] [Related]
15. Clinical and neurophysiological development of Unverricht-Lundborg disease in four Swedish siblings. Kyllerman M; Sommerfelt K; Hedström A; Wennergren G; Holmgren D Epilepsia; 1991; 32(6):900-9. PubMed ID: 1743164 [TBL] [Abstract][Full Text] [Related]
17. Progressive myoclonus epilepsy of Unverricht-Lundborg type: a clinical and molecular genetic study of a family from the United States with four affected sibs. Lehesjoki AE; Eldridge R; Eldridge J; Wilder BJ; de la Chapelle A Neurology; 1993 Nov; 43(11):2384-6. PubMed ID: 8232963 [TBL] [Abstract][Full Text] [Related]