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Quoted phrase not found in phrase index: "anterior spinocerebellar tract"
Page 1
Hereditary Myelopathies.
Fink JK. Fink JK. Continuum (Minneap Minn). 2021 Feb 1;27(1):185-204. doi: 10.1212/CON.0000000000000934. Continuum (Minneap Minn). 2021. PMID: 33522742 Review.
RECENT FINDINGS: Rather than a disease, a disease process, or relating to specific cellular vulnerability, the term hereditary myelopathy refers to diverse inherited disorders in which major aspects of the clinical syndrome reflect disturbance of elements within the spinal cord ( …
RECENT FINDINGS: Rather than a disease, a disease process, or relating to specific cellular vulnerability, the term hereditary myelopathy re …
The Neuropathology of Spinocerebellar Ataxia Type 3/Machado-Joseph Disease.
Koeppen AH. Koeppen AH. Adv Exp Med Biol. 2018;1049:233-241. doi: 10.1007/978-3-319-71779-1_11. Adv Exp Med Biol. 2018. PMID: 29427106 Review.
Spinocerebellar ataxia type 3 (SCA-3)/Machado-Joseph disease (MJD), the most common autosomal dominant ataxia, affects many regions of the brain and spinal cord. ...The spinal cord shows total or subtotal loss of neurons in the dorsal nuclei, anterior horn cell atro …
Spinocerebellar ataxia type 3 (SCA-3)/Machado-Joseph disease (MJD), the most common autosomal dominant ataxia, affects many regions o …
An autopsy case of an aged patient with spinocerebellar ataxia type 2.
Ishida C, Komai K, Yonezawa K, Sakajiri K, Nitta E, Kawashima A, Yamada M. Ishida C, et al. Neuropathology. 2011 Oct;31(5):510-8. doi: 10.1111/j.1440-1789.2010.01176.x. Epub 2010 Dec 6. Neuropathology. 2011. PMID: 21134000 Review.
This patient was diagnosed genetically as having spinocerebellar ataxia type 2 (SCA2), and the number of expanded CAG repeats was 41. At autopsy, the brain weighed 965 g, and the brainstem, cerebellum, frontal convexity and spinal cord were atrophic. Neuronal loss and glio …
This patient was diagnosed genetically as having spinocerebellar ataxia type 2 (SCA2), and the number of expanded CAG repeats was 41. …
Proteasomal and autophagic degradative activities in spinal and bulbar muscular atrophy.
Rusmini P, Bolzoni E, Crippa V, Onesto E, Sau D, Galbiati M, Piccolella M, Poletti A. Rusmini P, et al. Neurobiol Dis. 2010 Nov;40(2):361-9. doi: 10.1016/j.nbd.2010.06.016. Epub 2010 Jul 16. Neurobiol Dis. 2010. PMID: 20621188 Review.
SBMA was the first identified member of a large class of neurodegenerative diseases now known as CAG-related diseases, which includes Huntington's disease (HD), several types of spinocerebellar ataxia (SCAs), and dentatorubral and pallidoluysian atrophy (DRPLA). The expand …
SBMA was the first identified member of a large class of neurodegenerative diseases now known as CAG-related diseases, which includes Huntin …
Coexistence of Huntington's disease and familial amyotrophic lateral sclerosis: case presentation.
Rubio A, Steinberg K, Figlewicz DA, MacDonald ME, Greenamyre T, Hamill R, Shoulson I, Powers JM. Rubio A, et al. Acta Neuropathol. 1996 Oct;92(4):421-7. doi: 10.1007/s004010050539. Acta Neuropathol. 1996. PMID: 8891076 Review.
Pathological lesions also included loss of neurons and gliosis in the anterior horns, Clarke's columns and the hypoglossal nuclei; degeneration of the lateral corticospinal tracts, dorsal spinocerebellar tracts and fasciculus gracilis; and rare Bunina …
Pathological lesions also included loss of neurons and gliosis in the anterior horns, Clarke's columns and the hypoglossal nuclei; de …
Partial hypotrophy of the posterior and lateral columns of the spinal cord, representing a sequela of schistosomiasis mansoni: report of an autopsied case and a review of the literature.
Pittella JE. Pittella JE. Clin Neuropathol. 1989 Nov-Dec;8(6):257-62. Clin Neuropathol. 1989. PMID: 2515929 Review.
At autopsy there was old necrosis of most of the gray matter in the middle thoracic segment of the spinal cord and severe hypotrophy of the posterior columns in the lumbar spinal cord, of the posterior and anterior spinocerebellar tracts, and of the lateral c …
At autopsy there was old necrosis of most of the gray matter in the middle thoracic segment of the spinal cord and severe hypotrophy of the …
[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. Yoshida M, et al. Rinsho Shinkeigaku. 1995 Jun;35(6):589-99. Rinsho Shinkeigaku. 1995. PMID: 8521632 Review. Japanese.
The most characteristic pathological findings common to both cases were the extremely mild involvement of the middle root zone of the posterior column, Clarke's nuclei and spinocerebellar tracts. The pattern of lower motor neuron system degeneration paralleled the d …
The most characteristic pathological findings common to both cases were the extremely mild involvement of the middle root zone of the poster …
[A clinicopathological study of two respirator-aided long-survival cases of amyotrophic lateral sclerosis].
Yoshida M, Murakami N, Hashizume Y, Itoh E, Takahashi A. Yoshida M, et al. Rinsho Shinkeigaku. 1992 Mar;32(3):259-65. Rinsho Shinkeigaku. 1992. PMID: 1628448 Review. Japanese.
The spinal cord was slightly wasted with atrophic anterior roots. The histopathological study demonstrated the typical pattern of ALS in spite of the prolonged survival with artificial respiration. ...The pattern of white matter degeneration in the cord indicated some pall …
The spinal cord was slightly wasted with atrophic anterior roots. The histopathological study demonstrated the typical pattern of ALS …
[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. Terao S, et al. Rinsho Shinkeigaku. 1991 Sep;31(9):960-9. Rinsho Shinkeigaku. 1991. PMID: 1769159 Review. Japanese.
Pathologically, five cases showed multiple system degenerations including the middle root zone of the posterior columns, Clarke's nuclei and posterior spinocerebellar tracts as well as the ventral horns and pyramidal tracts, which were designated as the form …
Pathologically, five cases showed multiple system degenerations including the middle root zone of the posterior columns, Clarke's nuclei and …