139 related articles for article (PubMed ID: 3474092)
21. [Genetic heterogeneity of familial motor neuron disease].
Kondo K
No To Shinkei; 1989 Mar; 41(3):225-8. PubMed ID: 2667587
[No Abstract] [Full Text] [Related]
22. 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; 13(18):2031-42. PubMed ID: 15269181
[TBL] [Abstract][Full Text] [Related]
23. Sensory neuron degeneration in familial Kugelberg-Welander disease.
Winder TR; Auer RN
Can J Neurol Sci; 1989 Feb; 16(1):67-70. PubMed ID: 2924211
[TBL] [Abstract][Full Text] [Related]
24. 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; 1991-1992; 25-26():60-9. PubMed ID: 11980064
[TBL] [Abstract][Full Text] [Related]
25. Amyotrophic lateral sclerosis.
Gordon PH; Mitsumoto H; Hays AP
Sci Aging Knowledge Environ; 2003 Sep; 2003(35):dn2. PubMed ID: 12954882
[TBL] [Abstract][Full Text] [Related]
26. An autopsy case of atypical infantile motor neuron disease with hyaline intraneuronal inclusions.
Yokochi K; Oda M; Satoh J; Morimatsu Y
Arch Neurol; 1989 Jan; 46(1):103-7. PubMed ID: 2462862
[TBL] [Abstract][Full Text] [Related]
27. [A case of carcinomatous neuropathy with degeneration of posterior spinal column on MRI].
Yamamoto K; Takeuchi M; Yamauchi T; Maruyama S
Rinsho Shinkeigaku; 1993 Apr; 33(4):416-21. PubMed ID: 8396518
[TBL] [Abstract][Full Text] [Related]
28. [Clinico-pathological investigation of two patients with dementia with motor neuron disease].
Yamamoto R; Iseki E; Murayama N; Minegishi M; Kimura M; Eto K; Arai H; Ohbu S; Hatanaka D; Hino H; Fujisawa K
Brain Nerve; 2007 Mar; 59(3):263-9. PubMed ID: 17370652
[TBL] [Abstract][Full Text] [Related]
29. [A clinicopathological study of a patient with paraneoplastic limbic encephalitis, myelitis, sensory neuropathy and cerebellar degeneration, associated with a unique antineuronal antibody].
Yoshioka A; Saigan T; Ueda Y; Sakai K; Hirose G
Rinsho Shinkeigaku; 1993 Apr; 33(4):369-76. PubMed ID: 8396516
[TBL] [Abstract][Full Text] [Related]
30. 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; 268(1-2):140-4. PubMed ID: 18191946
[TBL] [Abstract][Full Text] [Related]
31. Unusual particles in motor neuron disease.
Averback P
Arch Pathol Lab Med; 1981 Sep; 105(9):490-3. PubMed ID: 6895022
[TBL] [Abstract][Full Text] [Related]
32. [Morphological changes in the central nervous system in amyotrophic leukospongiosis].
Nedźved' MK; Protas II; Votiakov VI; Antonov IP; Rytik PG
Arkh Patol; 1982; 44(10):60-6. PubMed ID: 6101250
[TBL] [Abstract][Full Text] [Related]
33. Widespread loss of neuronal populations in the spinal ventral horn in sporadic motor neuron disease. A morphometric study.
Stephens B; Guiloff RJ; Navarrete R; Newman P; Nikhar N; Lewis P
J Neurol Sci; 2006 May; 244(1-2):41-58. PubMed ID: 16487542
[TBL] [Abstract][Full Text] [Related]
34. Familial motor neuron disease in Rottweiler dogs: neuropathologic studies.
Shell LG; Jortner BS; Leib MS
Vet Pathol; 1987 Mar; 24(2):135-9. PubMed ID: 3576908
[TBL] [Abstract][Full Text] [Related]
35. [Machado-Joseph disease in a family of Spanish origin].
Pou-Serradell A; Russi A; Ferrer I; Galofré E; Escudero D
Rev Neurol (Paris); 1987; 143(6-7):520-5. PubMed ID: 3477847
[TBL] [Abstract][Full Text] [Related]
36. [A case of severe involvement of the motor neuron system accompanied with cerebellar ataxia].
Horiuchi I; Furuya H; Yoshimura T; Kobayashi T; Kusunoki S
Rinsho Shinkeigaku; 1997 Feb; 37(2):123-6. PubMed ID: 9164144
[TBL] [Abstract][Full Text] [Related]
37. Motor neuron disease and adult hexosaminidase A deficiency in two families: evidence for multisystem degeneration.
Mitsumoto H; Sliman RJ; Schafer IA; Sternick CS; Kaufman B; Wilbourn A; Horwitz SJ
Ann Neurol; 1985 Apr; 17(4):378-85. PubMed ID: 3159334
[TBL] [Abstract][Full Text] [Related]
38. Sporadic four-repeat tauopathy with frontotemporal degeneration, parkinsonism and motor neuron disease.
Piao YS; Tan CF; Iwanaga K; Kakita A; Takano H; Nishizawa M; Lashley T; Revesz T; Lees A; de Silva R; Tsujihata M; Takahashi H
Acta Neuropathol; 2005 Dec; 110(6):600-9. PubMed ID: 16328530
[TBL] [Abstract][Full Text] [Related]
39. [Infantile neuro-axonal dystrophy: anatomo clinical study of one case (author's transl)].
Onnis L; Nardelli E; Buonanno F; Galiazzo-Rizzuto S; Panizon F; Rizzuto N
Riv Patol Nerv Ment; 1975; 96(5):322-39. PubMed ID: 1235007
[TBL] [Abstract][Full Text] [Related]
40. Selective and asymmetric vulnerability of corticospinal and spinocerebellar tracts in motor neuron disease.
Swash M; Scholtz CL; Vowles G; Ingram DA
J Neurol Neurosurg Psychiatry; 1988 Jun; 51(6):785-9. PubMed ID: 3165441
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
