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Journal Abstract Search

335 related items for PubMed ID: 5006319

  • 1. [Familial progressive myoclonus epilepsy (Unverricht/Lundborg)].
    Herbst A.
    Psychiatr Neurol Med Psychol Beih; 1967; 6():18-39. PubMed ID: 5006319
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  • 2. [Familial progressive myoclonus epilepsy (pme) (type Unverricht)].
    Herbstund A, Schröter P.
    Psychiatr Neurol Med Psychol Beih; 1973; 17-18():100-17. PubMed ID: 4220172
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  • 8. [Myoclonic epilepsies in infancy].
    Palencia R.
    Rev Neurol; 2000 Jun; 30 Suppl 1():S15-24. PubMed ID: 10904965
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  • 9. [Unverricht-Lundborg myoclonic epilepsy in 3 siblings].
    Jezierska K, Nawrocka I.
    Neurol Neurochir Pol; 1971 Jun; 5(2):241-4. PubMed ID: 4252636
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  • 10. [A case of familial essential myoclonus and epilepsy with suspected focus in the hemisphere ipsilateral to myoclonus limbs].
    Asai H, Udaka F, Oishi N, Kubori T, Kameyama M.
    No To Shinkei; 2004 Jun; 56(6):509-13. PubMed ID: 15328840
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  • 12. A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23.
    Gribaa M, Salih M, Anheim M, Lagier-Tourenne C, H'mida D, Drouot N, Mohamed A, Elmalik S, Kabiraj M, Al-Rayess M, Almubarak M, Bétard C, Goebel H, Koenig M.
    Brain; 2007 Jul; 130(Pt 7):1921-8. PubMed ID: 17470496
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  • 17. Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation.
    Lebas A, Guyant-Maréchal L, Hannequin D, Riant F, Tournier-Lasserve E, Parain D.
    Cephalalgia; 2008 Jul; 28(7):774-7. PubMed ID: 18498390
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  • 19. Juvenile myoclonic epilepsy of Janz: clinical observations in 60 patients.
    Canevini MP, Mai R, Di Marco C, Bertin C, Minotti L, Pontrelli V, Saltarelli A, Canger R.
    Seizure; 1992 Dec; 1(4):291-8. PubMed ID: 1344779
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