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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

113 related items for PubMed ID: 4252636

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  • 3. [Progressive myoclonus epilepsy in two siblings and 5 cases with dyssynergia cerebellaris myoclonica in several generations of a kinship, a clinical and genetic study].
    Diebold K, Kastner M, Penin H.
    Nervenarzt; 1974 Nov; 45(11):595-601. PubMed ID: 4217888
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  • 4. 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
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  • 9. 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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  • 10. [On the differential diagnosis of progressive myoclonic epilepsy].
    Diebold K.
    Fortschr Neurol Psychiatr Grenzgeb; 1968 Oct; 36(10):545-75. PubMed ID: 4974222
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  • 12. [Familial myoclonus-renal failure syndrome].
    Rothdach AJ, Dietl T, Kümpfel T, Gottschalk M, Schumann EM, Trenkwalder C.
    Nervenarzt; 2001 Aug; 72(8):636-40. PubMed ID: 11519206
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  • 14. [Siblings with myoclonus corpuscle disease (Unverricht-Lundborg). Family and longitudinal section study].
    Barolin GS, Pateisky K.
    Wien Z Nervenheilkd Grenzgeb; 1969 Aug; 27(1):1-8. PubMed ID: 4241179
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  • 16. Unverricht-Lundborg progressive myoclonus epilepsy in Oman.
    Santoshkumar B, Turnbull J, Minassian BA.
    Pediatr Neurol; 2008 Apr; 38(4):252-5. PubMed ID: 18358403
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  • 17. [Clinical problems in epilepsy].
    Janz D.
    Nervenarzt; 1970 Feb; 41(2):53-8. PubMed ID: 4984829
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