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145 related items for PubMed ID: 2544822
1. A study of infantile motor neuron disease with neurofilament and ubiquitin immunocytochemistry. Lee S, Park YD, Yen SH, Ksiezak-Reding H, Goldman JE, Dickson DW. Neuropediatrics; 1989 May; 20(2):107-11. PubMed ID: 2544822 [Abstract] [Full Text] [Related]
3. Neurofilament phosphorylation in axons and perikarya: immunofluorescence study of the rat spinal cord and dorsal root ganglia with monoclonal antibodies. Dahl D, Labkovsky B, Bignami A. J Comp Neurol; 1988 May 15; 271(3):445-50. PubMed ID: 3133402 [Abstract] [Full Text] [Related]
4. Phosphate dependent and independent neurofilament epitopes in the axonal swellings of patients with motor neuron disease and controls. Schmidt ML, Carden MJ, Lee VM, Trojanowski JQ. Lab Invest; 1987 Mar 15; 56(3):282-94. PubMed ID: 2434727 [Abstract] [Full Text] [Related]
5. Neuropathological analysis in spinal muscular atrophy type II. Araki S, Hayashi M, Tamagawa K, Saito M, Kato S, Komori T, Sakakihara Y, Mizutani T, Oda M. Acta Neuropathol; 2003 Nov 15; 106(5):441-8. PubMed ID: 12898156 [Abstract] [Full Text] [Related]
6. Ubiquitin and phosphorylated neurofilament epitopes in ballooned neurons of the extraocular muscle nuclei in a case of Werdnig-Hoffmann disease. Kato S, Hirano A. Acta Neuropathol; 1990 Nov 15; 80(3):334-7. PubMed ID: 1698008 [Abstract] [Full Text] [Related]
7. [Spinal pathology in spinal muscular atrophy in comparison with amyotrophic lateral sclerosis]. Urbanits S, Budka H. Wien Med Wochenschr; 1996 Nov 15; 146(9-10):199-200. PubMed ID: 9012211 [Abstract] [Full Text] [Related]
8. Synaptic defects in type I spinal muscular atrophy in human development. Martínez-Hernández R, Bernal S, Also-Rallo E, Alías L, Barceló MJ, Hereu M, Esquerda JE, Tizzano EF. J Pathol; 2013 Jan 15; 229(1):49-61. PubMed ID: 22847626 [Abstract] [Full Text] [Related]
9. [Clinical and pathological study of motor neuron disease]. Tsukagoshi H. Rinsho Shinkeigaku; 1988 Dec 15; 28(12):1357-66. PubMed ID: 3254760 [No Abstract] [Full Text] [Related]
10. Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1). Grohmann K, Rossoll W, Kobsar I, Holtmann B, Jablonka S, Wessig C, Stoltenburg-Didinger G, Fischer U, Hübner C, Martini R, Sendtner M. Hum Mol Genet; 2004 Sep 15; 13(18):2031-42. PubMed ID: 15269181 [Abstract] [Full Text] [Related]
11. Ubiquitin in motor neuron disease: study at the light and electron microscope. Schiffer D, Autilio-Gambetti L, Chiò A, Gambetti P, Giordana MT, Gullotta F, Migheli A, Vigliani MC. J Neuropathol Exp Neurol; 1991 Jul 15; 50(4):463-73. PubMed ID: 1648124 [Abstract] [Full Text] [Related]
12. Immunocytochemical and ultrastructural studies of Werdnig-Hoffmann disease. Murayama S, Bouldin TW, Suzuki K. Acta Neuropathol; 1991 Jul 15; 81(4):408-17. PubMed ID: 1851364 [Abstract] [Full Text] [Related]
13. RNA-binding protein is involved in aggregation of light neurofilament protein and is implicated in the pathogenesis of motor neuron degeneration. Lin H, Zhai J, Schlaepfer WW. Hum Mol Genet; 2005 Dec 01; 14(23):3643-59. PubMed ID: 16236762 [Abstract] [Full Text] [Related]
14. 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 01; 105(6):615-20. PubMed ID: 12734667 [Abstract] [Full Text] [Related]
15. Aberrant glycosylation/phosphorylation in chromatolytic motoneurons of Werdnig-Hoffmann disease. Chou SM, Wang HS. J Neurol Sci; 1997 Nov 25; 152(2):198-209. PubMed ID: 9415542 [Abstract] [Full Text] [Related]
16. Distinct and overlapping alterations in motor and sensory neurons in a mouse model of spinal muscular atrophy. Jablonka S, Karle K, Sandner B, Andreassi C, von Au K, Sendtner M. Hum Mol Genet; 2006 Feb 01; 15(3):511-8. PubMed ID: 16396995 [Abstract] [Full Text] [Related]
17. Phosphorylation-dependent epitopes on neurofilament proteins and neurofilament densities differ in axons in the corticospinal and primary sensory dorsal column tracts in the rat spinal cord. Szaro BG, Whitnall MH, Gainer H. J Comp Neurol; 1990 Dec 08; 302(2):220-35. PubMed ID: 1705265 [Abstract] [Full Text] [Related]
18. Atypical motor neuron disease with features of a multisystem degeneration: a non-familial case with prominent sensory involvement. Moss TH, Campbell MJ. Clin Neuropathol; 1987 Dec 08; 6(2):55-60. PubMed ID: 3474092 [Abstract] [Full Text] [Related]
19. Neurofilament phosphorylation in neuronal perikarya following axotomy: a study of rat spinal cord with ventral and dorsal root transection. Mansour H, Bignami A, Labkovsky B, Dahl D. J Comp Neurol; 1989 May 22; 283(4):481-5. PubMed ID: 2501359 [Abstract] [Full Text] [Related]
20. Regionalized neurofilament accumulation and motoneuron degeneration are linked phenotypes in wobbler neuromuscular disease. Pernas-Alonso R, Perrone-Capano C, Volpicelli F, di Porzio U. Neurobiol Dis; 2001 Aug 22; 8(4):581-9. PubMed ID: 11493023 [Abstract] [Full Text] [Related] Page: [Next] [New Search]