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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

909 related items for PubMed ID: 11980064

  • 1. 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; ; 25-26():60-9. PubMed ID: 11980064
    [Abstract] [Full Text] [Related]

  • 2. [Two siblings of familial amyotrophic lateral sclerosis with multisystemic degeneration characterized by mild involvement of the middle root zone of the posterior column, Clarke's nuclei and spinocerebellar tract].
    Yoshida M, Okuda S, Murakami N, Hashizume Y, Sobue G.
    Rinsho Shinkeigaku; 1995 Jun; 35(6):589-99. PubMed ID: 8521632
    [Abstract] [Full Text] [Related]

  • 3. Amyotrophic lateral sclerosis: Part 1. Clinical features, pathology, and ethical issues in management.
    Tandan R, Bradley WG.
    Ann Neurol; 1985 Sep; 18(3):271-80. PubMed ID: 4051456
    [Abstract] [Full Text] [Related]

  • 4. [A clinicopathological study of familial amyotrophic lateral sclerosis with special reference to the mode of motoneuron loss in the spinal ventral horn].
    Terao S, Sobue G, Mukai E, Murakami N, Hashizume Y.
    Rinsho Shinkeigaku; 1991 Sep; 31(9):960-9. PubMed ID: 1769159
    [Abstract] [Full Text] [Related]

  • 5. [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]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity.
    Siddique T, Figlewicz DA, Pericak-Vance MA, Haines JL, Rouleau G, Jeffers AJ, Sapp P, Hung WY, Bebout J, McKenna-Yasek D.
    N Engl J Med; 1991 May 16; 324(20):1381-4. PubMed ID: 2020294
    [Abstract] [Full Text] [Related]

  • 8. [A clinicopathological study of two respirator-aided long-survival cases of amyotrophic lateral sclerosis].
    Yoshida M, Murakami N, Hashizume Y, Itoh E, Takahashi A.
    Rinsho Shinkeigaku; 1992 Mar 16; 32(3):259-65. PubMed ID: 1628448
    [Abstract] [Full Text] [Related]

  • 9. Asymmetric involvement of the spinal cord involving both large and small anterior horn cells in a case of familial amyotrophic lateral sclerosis.
    Kato T, Hirano A, Kurland LT.
    Clin Neuropathol; 1987 Mar 16; 6(2):67-70. PubMed ID: 3036409
    [Abstract] [Full Text] [Related]

  • 10. [Motor neuron diseases. Present].
    Pou A.
    Neurologia; 1996 Dec 16; 11 Suppl 5():1-6. PubMed ID: 9044569
    [Abstract] [Full Text] [Related]

  • 11. [Two autopsy cases of sporadic amyotrophic lateral sclerosis with 20-year-clinical course without respirators].
    Kato S, Oda M, Hayashi H, Komori T, Hirose K, Tanabe H, Arai N.
    No To Shinkei; 1993 Mar 16; 45(3):267-72. PubMed ID: 8323821
    [Abstract] [Full Text] [Related]

  • 12. Familial amyotrophic lateral sclerosis with Gly93Ser mutation in Cu/Zn superoxide dismutase: a clinical and neuropathological study.
    Suzuki M, Irie T, Watanabe T, Mikami H, Yamazaki T, Oyanagi K, Ono S.
    J Neurol Sci; 2008 May 15; 268(1-2):140-4. PubMed ID: 18191946
    [Abstract] [Full Text] [Related]

  • 13. Degeneration of the substantia nigra in familial amyotrophic lateral sclerosis.
    Wolf HK, Crain BJ, Siddique T.
    Clin Neuropathol; 1991 May 15; 10(6):291-6. PubMed ID: 1764852
    [Abstract] [Full Text] [Related]

  • 14. Degeneration of serotonergic neurons in amyotrophic lateral sclerosis: a link to spasticity.
    Dentel C, Palamiuc L, Henriques A, Lannes B, Spreux-Varoquaux O, Gutknecht L, René F, Echaniz-Laguna A, Gonzalez de Aguilar JL, Lesch KP, Meininger V, Loeffler JP, Dupuis L.
    Brain; 2013 Feb 15; 136(Pt 2):483-93. PubMed ID: 23114367
    [Abstract] [Full Text] [Related]

  • 15. Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.
    Hentati A, Bejaoui K, Pericak-Vance MA, Hentati F, Speer MC, Hung WY, Figlewicz DA, Haines J, Rimmler J, Ben Hamida C.
    Nat Genet; 1994 Jul 15; 7(3):425-8. PubMed ID: 7920663
    [Abstract] [Full Text] [Related]

  • 16. Primary lateral sclerosis, hereditary spastic paraplegia and amyotrophic lateral sclerosis: discrete entities or spectrum?
    Strong MJ, Gordon PH.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2005 Mar 15; 6(1):8-16. PubMed ID: 16036421
    [Abstract] [Full Text] [Related]

  • 17. Clinicopathologic features of autosomal recessive amyotrophic lateral sclerosis associated with optineurin mutation.
    Kamada M, Izumi Y, Ayaki T, Nakamura M, Kagawa S, Kudo E, Sako W, Maruyama H, Nishida Y, Kawakami H, Ito H, Kaji R.
    Neuropathology; 2014 Feb 15; 34(1):64-70. PubMed ID: 23889540
    [Abstract] [Full Text] [Related]

  • 18. 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 15; 105(6):615-20. PubMed ID: 12734667
    [Abstract] [Full Text] [Related]

  • 19. Familial amyotrophic lateral sclerosis with posterior column degeneration and basophilic inclusion bodies: a clinical, genetic and pathological study.
    Tsuchiya K, Matsunaga T, Aoki M, Haga C, Ooe K, Abe K, Ikeda K, Nakano I.
    Clin Neuropathol; 2001 Jun 15; 20(2):53-9. PubMed ID: 11327297
    [Abstract] [Full Text] [Related]

  • 20. [Neuropathology of the motor neuron disease--Bunina body].
    Kusaka H.
    Rinsho Shinkeigaku; 1999 Jan 15; 39(1):65-6. PubMed ID: 10377806
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 46.