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Journal Abstract Search

196 related items for PubMed ID: 11078211

  • 21. [Familial amyotrophic lateral sclerosis (FALS) with a novel SOD1 gene mutation: a clinicopathological study].
    Kawamata C, Morita M, Shibata N, Nakano I.
    Rinsho Shinkeigaku; 2007 May; 47(5):211-6. PubMed ID: 17585602
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  • 22. Recent advances in research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutations: neuronal Lewy body-like hyaline inclusions and astrocytic hyaline inclusions.
    Kato S, Saito M, Hirano A, Ohama E.
    Histol Histopathol; 1999 Jul; 14(3):973-89. PubMed ID: 10425565
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  • 23. Neuropathological changes in two lines of mice carrying a transgene for mutant human Cu,Zn SOD, and in mice overexpressing wild type human SOD: a model of familial amyotrophic lateral sclerosis (FALS).
    Dal Canto MC, Gurney ME.
    Brain Res; 1995 Apr 03; 676(1):25-40. PubMed ID: 7796176
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  • 24. Clinical and pathological studies of familial amyotrophic lateral sclerosis (FALS) with SOD1 H46R mutation in large Japanese families.
    Arisato T, Okubo R, Arata H, Abe K, Fukada K, Sakoda S, Shimizu A, Qin XH, Izumo S, Osame M, Nakagawa M.
    Acta Neuropathol; 2003 Dec 03; 106(6):561-8. PubMed ID: 14517684
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  • 29. Familial ALS with FUS P525L mutation: two Japanese sisters with multiple systems involvement.
    Mochizuki Y, Isozaki E, Takao M, Hashimoto T, Shibuya M, Arai M, Hosokawa M, Kawata A, Oyanagi K, Mihara B, Mizutani T.
    J Neurol Sci; 2012 Dec 15; 323(1-2):85-92. PubMed ID: 22980027
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  • 30. Distinctive clinicopathological features of 2 large families with amyotrophic lateral sclerosis having L106V mutation in SOD1 gene.
    Hineno A, Nakamura A, Shimojima Y, Yoshida K, Oyanagai K, Ikeda S.
    J Neurol Sci; 2012 Aug 15; 319(1-2):63-74. PubMed ID: 22647583
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  • 31. Clinical characteristics of familial amyotrophic lateral sclerosis with Cu/Zn superoxide dismutase gene mutations.
    Abe K, Aoki M, Ikeda M, Watanabe M, Hirai S, Itoyama Y.
    J Neurol Sci; 1996 Mar 15; 136(1-2):108-16. PubMed ID: 8815157
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  • 34. 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 15; 250(2):164-70. PubMed ID: 12574946
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  • 35. Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene.
    Giess R, Holtmann B, Braga M, Grimm T, Müller-Myhsok B, Toyka KV, Sendtner M.
    Am J Hum Genet; 2002 May 15; 70(5):1277-86. PubMed ID: 11951178
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  • 36. 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
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  • 37. Forme fruste or incipient form of widespread-type amyotrophic lateral sclerosis, or motor neuron disease with pallido-nigro-luysian atrophy? An autopsy case report.
    Hashimoto T, Matsubara S, Mochizuki Y, Tsuji S, Mizutani T, Oyanagi K.
    Neuropathology; 2008 Jun 15; 28(3):309-16. PubMed ID: 18179405
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  • 38. Familial amyotrophic lateral sclerosis with a novel G85S mutation of superoxide dismutase 1 gene: clinical features of lower motor neuron disease.
    Takazawa T, Ikeda K, Hirayama T, Kawabe K, Nakamura Y, Ito H, Kano O, Yoshii Y, Tanaka F, Sobue G, Iwasaki Y.
    Intern Med; 2010 Jun 15; 49(2):183-6. PubMed ID: 20075587
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  • 39. An autopsy case of familial amyotrophic lateral sclerosis with a TARDBP Q343R mutation.
    Okamoto K, Fujita Y, Hoshino E, Tamura Y, Fukuda T, Hasegawa M, Takatama M.
    Neuropathology; 2015 Oct 15; 35(5):462-8. PubMed ID: 26096467
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  • 40. The Golgi apparatus is fragmented in spinal cord motor neurons of amyotrophic lateral sclerosis with basophilic inclusions.
    Fujita Y, Okamoto K, Sakurai A, Kusaka H, Aizawa H, Mihara B, Gonatas NK.
    Acta Neuropathol; 2002 Mar 15; 103(3):243-7. PubMed ID: 11907804
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