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Journal Abstract Search

191 related items for PubMed ID: 6439445

  • 1. Progressive myoclonic epilepsy, nerve deafness and spinal muscular atrophy.
    Lance JW, Evans WA.
    Clin Exp Neurol; 1984; 20():141-51. PubMed ID: 6439445
    [Abstract] [Full Text] [Related]

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

  • 3. [Dentatorubropallidoluysian atrophy (DRPLA): comparative pathological study on clinical groups classified into juvenile, early adult and late adult types].
    Takeda S, Takahashi H, Ikuta F.
    No To Shinkei; 1992 Feb; 44(2):111-6. PubMed ID: 1567729
    [Abstract] [Full Text] [Related]

  • 4. [Progressive myoclonic epilepsy: anatomo - clinical study of a sporadic case with a marked cerebellar symptomatology (author's transl)].
    Nardelli E, Buonanno F, Onnis L, Rizzuto N.
    Riv Patol Nerv Ment; 1975 Feb; 96(4):221-32. PubMed ID: 1232666
    [Abstract] [Full Text] [Related]

  • 5. Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literature.
    Haliloglu G, Chattopadhyay A, Skorodis L, Manzur A, Mercuri E, Talim B, Akçören Z, Renda Y, Muntoni F, Topaloğlu H.
    Neuropediatrics; 2002 Dec; 33(6):314-9. PubMed ID: 12571787
    [Abstract] [Full Text] [Related]

  • 6. 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 24; 68(17):1382-9. PubMed ID: 17452583
    [Abstract] [Full Text] [Related]

  • 7. [Progressive familial myoclonic epilepsy with bulbo-spinal amyotrophy. Clinical, electrophysiological study, and biopsy of a case].
    Taglioli M, Bartolini S, Volpi G, Alberti G, Ambrosetto G.
    Riv Neurol; 1990 Apr 24; 60(5):201-6. PubMed ID: 2151603
    [Abstract] [Full Text] [Related]

  • 8. Familial occurrence of myoclonic epilepsy syndrome and acute intermittent porphyria.
    Varsik P, Buranová D, Kollár B, Traubner P, Bozek P, Mikulecký M.
    Neuro Endocrinol Lett; 2005 Feb 24; 26(1):7-12. PubMed ID: 15726012
    [Abstract] [Full Text] [Related]

  • 9. Ramsay Hunt syndrome: progressive mental deterioration in association with unusual cerebral white matter change.
    Kobayashi K, Morikawa K, Fukutani Y, Miyazu K, Nakamura I, Yamaguchi N, Watanabe H.
    Clin Neuropathol; 1994 Feb 24; 13(2):88-96. PubMed ID: 8205732
    [Abstract] [Full Text] [Related]

  • 10. Juvenile neuroaxonal dystrophy: clinical, electrophysiological, and neuropathological features.
    Dorfman LJ, Pedley TA, Tharp BR, Scheithauer BW.
    Ann Neurol; 1978 May 24; 3(5):419-28. PubMed ID: 103487
    [Abstract] [Full Text] [Related]

  • 11. Association of lower motor neuron disorders with fasciculation, neuromyotonia and myoclonus.
    Lance JW.
    Aust Paediatr J; 1988 May 24; 24 Suppl 1():113-5. PubMed ID: 3144266
    [Abstract] [Full Text] [Related]

  • 12. Bulbo-spinal lower motor neuron disease. Accumulation of neurofilaments in perikarya and axons.
    Martin JJ, Mercelis R, Dua G, Moens E.
    Acta Neurol Belg; 1982 May 24; 82(5):262-9. PubMed ID: 6890751
    [Abstract] [Full Text] [Related]

  • 13. [An autopsy case with lower motor neuron disease showing a transient-appearance of anti-GM1 antibody and an improvement of conduction block after gamma-globulin administration].
    Kikuchi H, Kawano Y, Dohura K, Kawamura T, Taniwaki T, Yamada T, Kato M, Iwaki T, Kira J.
    No To Shinkei; 1999 May 24; 51(5):455-64. PubMed ID: 10396755
    [Abstract] [Full Text] [Related]

  • 14. [Progressive supranuclear palsy: description of a case of early occurrence associated with muscular atrophies (author's transl)].
    Barontini F, Cappelli L, Marconi G.
    Riv Patol Nerv Ment; 1978 May 24; 99(4):195-206. PubMed ID: 752181
    [Abstract] [Full Text] [Related]

  • 15. Lower motor neuron disease with spinocerebellar degeneration.
    Page RW, Moskowitz RW, Nash RE, Roessmann U.
    Ann Neurol; 1977 Dec 24; 2(6):524-7. PubMed ID: 617594
    [Abstract] [Full Text] [Related]

  • 16. Sensory ganglioneuropathy in infantile spinal muscular atrophy. Light and electronmicroscopic findings in two cases.
    Probst A, Ulrich J, Bischoff A, Boltshauser E.
    Neuropediatrics; 1981 Aug 24; 12(3):215-31. PubMed ID: 7290343
    [Abstract] [Full Text] [Related]

  • 17. 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 Aug 24; 67():181-97. PubMed ID: 8848969
    [Abstract] [Full Text] [Related]

  • 18. Late infantile neuroaxonal dystrophy. An unusual case with predominantly myoclonic-epileptic symptomatology.
    Barontini F, Papini M.
    Riv Patol Nerv Ment; 1981 Aug 24; 101(4):171-84. PubMed ID: 6789439
    [Abstract] [Full Text] [Related]

  • 19. [Study of androgen receptor expression and neuronal vulnerability in X-linked spinal and bulbar muscular atrophy].
    Matsuura T.
    Hokkaido Igaku Zasshi; 1996 Nov 24; 71(6):785-99. PubMed ID: 8996845
    [Abstract] [Full Text] [Related]

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

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