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 *

107 related articles for article (PubMed ID: 2418650)

  • 1. Baltic myoclonus.
    Koskiniemi ML
    Adv Neurol; 1986; 43():57-64. PubMed ID: 2418650
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Effect of phenytoin on the mental and physical function of patients with Baltic myoclonus epilepsy.
    Iivanainen M; Eldridge R
    Ital J Neurol Sci; 1987 Aug; 8(4):313-7. PubMed ID: 3119515
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Progressive myoclonic epilepsy: A clinical, electrophysiological and pathological study from South India.
    Sinha S; Satishchandra P; Gayathri N; Yasha TC; Shankar SK
    J Neurol Sci; 2007 Jan; 252(1):16-23. PubMed ID: 17166519
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Myoclonic epilepsies in infancy].
    Palencia R
    Rev Neurol; 2000 Jun; 30 Suppl 1():S15-24. PubMed ID: 10904965
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Benign myoclonic epilepsy in infants: electroclinical features and long-term follow-up of 34 patients.
    Auvin S; Pandit F; De Bellecize J; Badinand N; Isnard H; Motte J; Villeneuve N; Lamblin MD; Vallée L
    Epilepsia; 2006 Feb; 47(2):387-93. PubMed ID: 16499765
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Epileptic negative myoclonus.
    Tassinari CA; Rubboli G; Parmeggiani L; Valzania F; Plasmati R; Riguzzi P; Michelucci R; Volpi L; Passarelli D; Meletti S
    Adv Neurol; 1995; 67():181-97. PubMed ID: 8848969
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Action myoclonus, Ramsay Hunt syndrome, and other cerebellar myoclonic syndromes.
    Lance JW
    Adv Neurol; 1986; 43():33-55. PubMed ID: 3080851
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The molecular genetic bases of the progressive myoclonus epilepsies.
    Serratosa JM; Gardiner RM; Lehesjoki AE; Pennacchio LA; Myers RM
    Adv Neurol; 1999; 79():383-98. PubMed ID: 10514828
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Unverricht-Lundborg progressive myoclonus epilepsy in Oman.
    Santoshkumar B; Turnbull J; Minassian BA
    Pediatr Neurol; 2008 Apr; 38(4):252-5. PubMed ID: 18358403
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. [Unverricht-Lündborg disease: clinical and electrophysiologic study of 19 Maghreb families].
    Gouider R; Ibrahim S; Fredj M; Gargouri A; Saïdi H; Ouezzani R; Malafosse A; Yahiaoui M; Grid D; Mrabet A
    Rev Neurol (Paris); 1998 Jul; 154(6-7):503-7. PubMed ID: 9773083
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Reflex myoclonic epilepsy in infancy: a new reflex epilepsy syndrome or a variant of benign myoclonic epilepsy in infancy].
    Caraballo R; Cassar L; Monges S; Yepez I; Galicchio S; Cersósimo R; Fejerman N
    Rev Neurol; 2003 Mar 1-15; 36(5):429-32. PubMed ID: 12640595
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Myoclonus in neuronal storage and Lafora diseases.
    Rapin I
    Adv Neurol; 1986; 43():65-85. PubMed ID: 3080854
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Deficient intestinal absorption of L-tryptophan in progressive myoclonus epilepsy without Lafora bodies.
    Koskiniemi ML
    J Neurol Sci; 1980 Jul; 47(1):1-6. PubMed ID: 6157783
    [TBL] [Abstract][Full Text] [Related]  

  • 18. "Baltic" myoclonus epilepsy: hereditary disorder of childhood made worse by phenytoin.
    Eldridge R; Iivanainen M; Stern R; Koerber T; Wilder BJ
    Lancet; 1983 Oct; 2(8354):838-42. PubMed ID: 6137660
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial cortical myoclonic tremor with epilepsy (FCMTE): Clinical characteristics and exclusion of linkages to 8q and 2p in a large French family.
    Magnin E; Vidailhet M; Depienne C; Saint-Martin C; Bouteiller D; LeGuern E; Apartis E; Rumbach L; Labauge P
    Rev Neurol (Paris); 2009 Oct; 165(10):812-20. PubMed ID: 19616813
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical picture of EPM1-Unverricht-Lundborg disease.
    Kälviäinen R; Khyuppenen J; Koskenkorva P; Eriksson K; Vanninen R; Mervaala E
    Epilepsia; 2008 Apr; 49(4):549-56. PubMed ID: 18325013
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.