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Journal Abstract Search

112 related items for PubMed ID: 7395463

  • 1. Familial amyotrophic lateral sclerosis. Report of a family with predominant upper limb pareses and late onset.
    Hestnes A, Mellgren SI.
    Acta Neurol Scand; 1980 Mar; 61(3):192-9. PubMed ID: 7395463
    [Abstract] [Full Text] [Related]

  • 2. [Familial amyotrophic lateral sclerosis with rapid progression].
    Oyama G, Izawa N, Fujishima K, Kobayashi H, Mizuno Y, Okuma Y.
    No To Shinkei; 2005 Nov; 57(11):1003-6. PubMed ID: 16363640
    [Abstract] [Full Text] [Related]

  • 3. A molecular genetic approach to amyotrophic lateral sclerosis.
    Siddique T, Hu P, Hentati A, Deng G, Hung WY, McInnis MG, Warren AC, Rimmler J, Antonarakis S, Pericak-Vance MA.
    Int J Neurol; 2005 Nov; 25-26():60-9. PubMed ID: 11980064
    [Abstract] [Full Text] [Related]

  • 4. A clinical and pathological study of a Japanese case of Amyotrophic Lateral Sclerosis/Parkinsonism-Dementia Complex with family history.
    Konagaya M, Kato T, Sakai M, Kuru S, Matsuoka Y, Konagaya Y, Hashizume Y, Tabira T.
    J Neurol; 2003 Feb; 250(2):164-70. PubMed ID: 12574946
    [Abstract] [Full Text] [Related]

  • 5. [Familial amytrophic lateral sclerosis. A study of a family suffering from this disease for three generations].
    Swerts L, Van Den Bergh R.
    J Genet Hum; 1976 Sep; 24(3):247-55. PubMed ID: 1003176
    [Abstract] [Full Text] [Related]

  • 6. [Amyotrophic lateral sclerosis that begins with voice and deglution alterations].
    Faubel Serra M, Pardo Mateu L, Perez Climent F, Llavero Segovia MT, Cano Cuenca B, Grau Alario E, Gimenez Vaillo F, Canals Ruiz P.
    An Otorrinolaringol Ibero Am; 2006 Sep; 33(3):273-80. PubMed ID: 16881554
    [Abstract] [Full Text] [Related]

  • 7. Juvenile amyotrophic lateral sclerosis. A report of two cases in a single family.
    Myllylä VV, Toivakka E, Ala-Hurula V, Hokkanen E, Emeryk-Szajewska B.
    Acta Neurol Scand; 1979 Sep; 60(3):170-7. PubMed ID: 517116
    [Abstract] [Full Text] [Related]

  • 8. [Clinical study of familial forms of amyotrophic lateral sclerosis. Review of the literature].
    Moulard B, Camu W, Malafosse A, Billiard M, Baldy-Moulinier M.
    Rev Neurol (Paris); 1997 Jun; 153(5):314-24. PubMed ID: 9296165
    [Abstract] [Full Text] [Related]

  • 9. [Familial amyotrophic lateral sclerosis showing variable clinical courses with (Leu84-->Val) mutation of Cu/Zn superoxide dismutase].
    Ohnishi A, Miyazaki S, Murai Y, Ueno S, Sakai H.
    Rinsho Shinkeigaku; 1996 Mar; 36(3):485-7. PubMed ID: 8741355
    [Abstract] [Full Text] [Related]

  • 10. Difficulties in distinguishing sporadic from familial amyotrophic lateral sclerosis.
    Orrell RW, Habgood J, Rudge P, Lane RJ, de Belleroche JS.
    Ann Neurol; 1996 Jun; 39(6):810-2. PubMed ID: 8651656
    [Abstract] [Full Text] [Related]

  • 11. [An apraxia of eyelid closure in association with frontal lobe atrophy in a patient with amyotrophic lateral sclerosis].
    Fukushima T, Hasegawa A, Matsubara N, Koike R.
    Rinsho Shinkeigaku; 2007 May; 47(5):226-30. PubMed ID: 17585605
    [Abstract] [Full Text] [Related]

  • 12. [On intra-familial clinical diversities of a familial amyotrophic lateral sclerosis with a point mutation of Cu/Zn superoxide dismutase (Asn 86-Ser].
    Maeda T, Kurahashi K, Matsunaga M, Inoue K, Inoue M.
    No To Shinkei; 1997 Sep; 49(9):847-51. PubMed ID: 9311004
    [Abstract] [Full Text] [Related]

  • 13. Familial amyotrophic lateral sclerosis with bulbar onset and a novel Asp101Tyr Cu/Zn superoxide dismutase gene mutation.
    Tan CF, Piao YS, Hayashi S, Obata H, Umeda Y, Sato M, Fukushima T, Nakano R, Tsuji S, Takahashi H.
    Acta Neuropathol; 2004 Oct; 108(4):332-6. PubMed ID: 15235802
    [Abstract] [Full Text] [Related]

  • 14. [Association of amyotrophic lateral sclerosis and multiple sclerosis].
    Confavreux C, Moreau T, Jouvet A, Tommasi M, Aimard G.
    Rev Neurol (Paris); 1993 Oct; 149(5):351-3. PubMed ID: 8272733
    [Abstract] [Full Text] [Related]

  • 15. A rare Cu/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset and incomplete penetrance in China.
    Zhang H, Zhao H, Lu M, Zhang Y, Wang L, Zhang J, Ma D, Fan D.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2005 Dec; 6(4):234-8. PubMed ID: 16319027
    [Abstract] [Full Text] [Related]

  • 16. [Etiology of lower brachial plexus pareses].
    Engel E, Neumärker M.
    Psychiatr Neurol Med Psychol (Leipz); 1969 Dec; 21(12):453-8. PubMed ID: 5373896
    [No Abstract] [Full Text] [Related]

  • 17. [Kugelberg-Welander type pseudomyopathic atrophy and amyotrophic lateral sclerosis].
    Kaeser HE, Wurmser P.
    Rev Neurol (Paris); 1968 Jun; 118(6):554-5. PubMed ID: 5724670
    [No Abstract] [Full Text] [Related]

  • 18. Natural history of young-adult amyotrophic lateral sclerosis.
    Sabatelli M, Madia F, Conte A, Luigetti M, Zollino M, Mancuso I, Lo Monaco M, Lippi G, Tonali P.
    Neurology; 2008 Sep 16; 71(12):876-81. PubMed ID: 18596241
    [Abstract] [Full Text] [Related]

  • 19. Primary lateral sclerosis: a rare upper-motor-predominant form of amyotrophic lateral sclerosis often accompanied by frontotemporal lobar degeneration with ubiquitinated neuronal inclusions? Report of an autopsy case and a review of the literature.
    Tan CF, Kakita A, Piao YS, Kikugawa K, Endo K, Tanaka M, Okamoto K, Takahashi H.
    Acta Neuropathol; 2003 Jun 16; 105(6):615-20. PubMed ID: 12734667
    [Abstract] [Full Text] [Related]

  • 20. [Juvenile and familial amyotrophic lateral sclerosis. 2 case reports (author's transl)].
    Saillant A, Fauchier C, Labarthe JC, Despert F, Combe P.
    Arch Fr Pediatr; 1981 Apr 16; 38(4):247-51. PubMed ID: 7294951
    [Abstract] [Full Text] [Related]

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