Literature DB >> 6018874

Familial amyotrophic lateral sclerosis. A subgroup characterized by posterior and spinocerebellar tract involvement and hyaline inclusions in the anterior horn cells.

A Hirano, L T Kurland, G P Sayre.   

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Year:  1967        PMID： 6018874     DOI： 10.1001/archneur.1967.00470210008002

Source DB:  PubMed          Journal:  Arch Neurol        ISSN： 0003-9942


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  46 in total

1.  Pathological characterization of astrocytic hyaline inclusions in familial amyotrophic lateral sclerosis.

Authors:  S Kato; H Hayashi; K Nakashima; E Nanba; M Kato; A Hirano; I Nakano; K Asayama; E Ohama
Journal:  Am J Pathol       Date:  1997-08       Impact factor: 4.307

2.  Sporadic amyotrophic lateral sclerosis with extensive neurological involvement.

Authors:  S Sasaki; Y Tsutsumi; K Yamane; H Sakuma; S Maruyama
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

3.  Widely distributed Bunina bodies and spheroids in a case of atypical sporadic amyotrophic lateral sclerosis.

Authors:  K Okamoto; S Hirai; M Shoji; Y Harigaya; T Fukuda
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

4.  A sporadic juvenile case of the amyotrophic lateral sclerosis with neuronal intracytoplasmic inclusions.

Authors:  M Oda; N Akagawa; Y Tabuchi; H Tanabe
Journal:  Acta Neuropathol       Date:  1978-12-15       Impact factor: 17.088

5.  Immunocytochemical and ultrastructural studies of hyaline inclusions in sporadic motor neuron disease.

Authors:  S Sasaki; S Maruyama
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

6.  Fine structural changes in the mutant hamster with hind leg paralysis.

Authors:  A Hirano
Journal:  Acta Neuropathol       Date:  1977-08-31       Impact factor: 17.088

7.  Is Werdnig-Hoffmann disease a pure lower motor neuron disorder?

Authors:  J Towfighi; R S Young; R M Ward
Journal:  Acta Neuropathol       Date:  1985       Impact factor: 17.088

8.  Focal accumulation of phosphorylated neurofilaments within anterior horn cell in familial amyotrophic lateral sclerosis.

Authors:  H Mizusawa; S Matsumoto; S H Yen; A Hirano; R R Rojas-Corona; H Donnenfeld
Journal:  Acta Neuropathol       Date:  1989       Impact factor: 17.088

9.  The Golgi apparatus of spinal cord motor neurons in transgenic mice expressing mutant Cu,Zn superoxide dismutase becomes fragmented in early, preclinical stages of the disease.

Authors:  Z Mourelatos; N K Gonatas; A Stieber; M E Gurney; M C Dal Canto
Journal:  Proc Natl Acad Sci U S A       Date:  1996-05-28       Impact factor: 11.205

10.  Genome-wide association analysis reveals a SOD1 mutation in canine degenerative myelopathy that resembles amyotrophic lateral sclerosis.

Authors:  Tomoyuki Awano; Gary S Johnson; Claire M Wade; Martin L Katz; Gayle C Johnson; Jeremy F Taylor; Michele Perloski; Tara Biagi; Izabella Baranowska; Sam Long; Philip A March; Natasha J Olby; G Diane Shelton; Shahnawaz Khan; Dennis P O'Brien; Kerstin Lindblad-Toh; Joan R Coates
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-02       Impact factor: 11.205
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