These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

120 related articles for article (PubMed ID: 9186245)

  • 1. Familial Unverricht-Lundborg disease: a clinical, neurophysiologic, and genetic study.
    Parmeggiani A; Lehesjoki AE; Carelli V; Posar A; Santi A; Santucci M; Gobbi G; Pini A; Rossi PG
    Epilepsia; 1997 Jun; 38(6):637-41. PubMed ID: 9186245
    [TBL] [Abstract][Full Text] [Related]  

  • 2. PME of Unverricht-Lundborg type in the Mediterranean region: linkage and linkage disequilibrium confirm the assignment to the EPM1 locus.
    Lehesjoki AE; Tassinari CA; Avanzini G; Michelucci R; Franceschetti S; Antonelli A; Rubboli G; de la Chapelle A
    Hum Genet; 1994 Jun; 93(6):668-74. PubMed ID: 8005591
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Lafora disease is not linked to the Unverricht-Lundborg locus.
    Labauge P; Beck C; Bellet H; Coquillat G; Vespignani H; Dulac O; Gilgenkrantz S; Dravet C; Genton P; Pellissier JF
    Am J Med Genet; 1995 Feb; 60(1):80-4. PubMed ID: 7485240
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q.
    Virtaneva K; Miao J; Träskelin AL; Stone N; Warrington JA; Weissenbach J; Myers RM; Cox DR; Sistonen P; de la Chapelle A
    Am J Hum Genet; 1996 Jun; 58(6):1247-53. PubMed ID: 8651302
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Unverricht-Lundborg disease: absence of nonallelic genetic heterogeneity.
    Cochius JI; Figlewicz DA; Kälviäinen R; Nousiainen U; Farrell K; Patry G; Söderfeldt B; Frydman M; Lerman P; Andermann F
    Ann Neurol; 1993 Nov; 34(5):739-41. PubMed ID: 8239570
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Progressive myoclonus epilepsies: clinical and genetic aspects.
    Berkovic SF; Cochius J; Andermann E; Andermann F
    Epilepsia; 1993; 34 Suppl 3():S19-30. PubMed ID: 8500430
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Allelic heterogeneity of Mediterranean myoclonus and the cystatin B gene.
    Labauge P; Ouazzani R; M'Rabet A; Grid D; Genton P; Dravet C; Chkili T; Beck C; Buresi C; Baldy-Moulinier M; Malafosse A
    Ann Neurol; 1997 May; 41(5):686-9. PubMed ID: 9153533
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Progressive myoclonus epilepsy of Unverricht-Lundborg type.
    Lehesjoki AE; Koskiniemi M
    Epilepsia; 1999; 40 Suppl 3():23-8. PubMed ID: 10446747
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1.
    Lafrenière RG; Rochefort DL; Chrétien N; Rommens JM; Cochius JI; Kälviäinen R; Nousiainen U; Patry G; Farrell K; Söderfeldt B; Federico A; Hale BR; Cossio OH; Sørensen T; Pouliot MA; Kmiec T; Uldall P; Janszky J; Pranzatelli MR; Andermann F; Andermann E; Rouleau GA
    Nat Genet; 1997 Mar; 15(3):298-302. PubMed ID: 9054946
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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. Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping.
    Lehesjoki AE; Koskiniemi M; Norio R; Tirrito S; Sistonen P; Lander E; de la Chapelle A
    Hum Mol Genet; 1993 Aug; 2(8):1229-34. PubMed ID: 8104628
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1).
    Pennacchio LA; Lehesjoki AE; Stone NE; Willour VL; Virtaneva K; Miao J; D'Amato E; Ramirez L; Faham M; Koskiniemi M; Warrington JA; Norio R; de la Chapelle A; Cox DR; Myers RM
    Science; 1996 Mar; 271(5256):1731-4. PubMed ID: 8596935
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial progressive myoclonus epilepsy: clinical and electrophysiologic observations.
    Acharya JN; Satishchandra P; Shankar SK
    Epilepsia; 1995 May; 36(5):429-34. PubMed ID: 7614918
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Electroclinical and genetic findings in a family with cortical tremor, myoclonus, and epilepsy.
    Striano P; Madia F; Minetti C; Striano S; Zara F
    Epilepsia; 2005 Dec; 46(12):1993-5. PubMed ID: 16393167
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Progressive myoclonus epilepsies. Criteria for diagnosis on the basis of the follow-up of 37 cases.
    Guazzi GC; Federico A
    Acta Neurol (Napoli); 1992; 14(4-6):469-84. PubMed ID: 1293989
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical, neuropsychological, neurophysiologic, and genetic features of a new Italian pedigree with familial cortical myoclonic tremor with epilepsy.
    Suppa A; Berardelli A; Brancati F; Marianetti M; Barrano G; Mina C; Pizzuti A; Sideri G
    Epilepsia; 2009 May; 50(5):1284-8. PubMed ID: 19222544
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Familial progressive myoclonus epilepsy (Unverricht/Lundborg)].
    Herbst A
    Psychiatr Neurol Med Psychol Beih; 1967; 6():18-39. PubMed ID: 5006319
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.