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1 y alpha-motor neuron loss in the spinal cord anterior horn.
2 bodies and processes of interneurons in the anterior horn.
3 microdissection and one from the surrounding anterior horns.
5 few GFAP-cells in Layer II in the SVZ of the anterior horn and the body of the lateral ventricle appe
6 onal loss in the lower cranial nerve nuclei, anterior horns and corresponding nerves, atrophy of the
9 non-immune forms of PNH that include toxins, anterior horn cell degeneration in motor neurone disease
11 re syndrome 1 and lethal arthrogryposis with anterior horn cell disease are autosomal recessive fetal
13 41 million (95% CI, $1132-$1351 million) for anterior horn cell disease; $75 million (95% CI, $57-$92
15 oma-spinal cord-34 motor neurons and primary anterior horn cell neurons showed that IL-6 exerted a ne
21 of the central grey matter, with predominant anterior horn-cell involvement, and nine (75%) children
23 udy is to investigate the involvement of the anterior horn cells (AHC) in the early post-stroke perio
25 ed atrophic spinal cords with marked loss of anterior horn cells and degeneration of corticospinal tr
26 d disorders characterized by degeneration of anterior horn cells and progressive muscle weakness.
28 atrophy, there is selective degeneration of anterior horn cells but a normal corticospinal tract.
29 Virus antigen was localized predominantly to anterior horn cells in infected IFN-gamma(-/-) H-2(q) mi
34 aracterized by selective degeneration of the anterior horn cells with subsequent weakness and atrophy
35 only to the primary cells of the periphery (anterior horn cells, motor axons and primary afferent se
41 erebral and brainstem neurons to spinal cord anterior horn cells; thus, severe poliomyelitis, but not
44 eus, and paraventricular nucleus, and in the anterior horn, interomediolateral cell column, and Clark
45 both transgenic mouse and human spinal cord anterior horn motor neurons, indicating that members of
47 erior columns of the spinal cord and loss of anterior horn neurons but without other involvement of t
48 oreactive inclusions were observed in spinal anterior horn neurons in all SALS and FALS cases, except
49 ic LDVs possess the unique ability to infect anterior horn neurons of ADPM-susceptible mice, they exh
50 gic analysis demonstrated dramatic injury to anterior horn neurons of IL-6-/- H-2q mice at 12 d after
51 c isolates in their unique ability to infect anterior horn neurons of immunosuppressed C58 and AKR mi
52 detected, along with moderate (47%) loss of anterior horn neurons, notably in demyelinating MS lesio
53 hat mHTT was preferably expressed within the anterior horn of the gray matter, in both cervical and l
54 nts), (g) cartilage thinning adjacent to the anterior horn of the lateral meniscus (in 19, 19, and 21
56 d speckled increased signal intensity at the anterior horn of the lateral meniscus near its central a
59 teoarthritis was induced by resection of the anterior horn of the medial meniscus and of the medial c
61 sorder affecting mainly motor neurons in the anterior horn of the spinal cord and brainstem motor nuc
62 and, to a lesser extent, glial cells in the anterior horn of the spinal cord exhibit robust Cox-2 im
63 gments are found in apoptotic neurons in the anterior horn of the spinal cord of affected transgenic
64 e that leads to loss of motor neurons in the anterior horn of the spinal cord with consequent muscle
65 ting/degenerated motor neurons in the lumbar anterior horn of the spinal cord, suggesting a direct ca
71 l, facial, and acoustic cranial ganglia; the anterior horns of the spinal cord in the region of the d
72 eatures of inflammation, particularly in the anterior horns of the spinal cord, the dorsal pons, and
73 of abnormal signal intensity confined to the anterior horns on a lumbar spine magnetic resonance imag
74 r horn was greater than that adjacent to the anterior horn (P <.05), and enhancement of the lateral m
75 sy; (2) laterally directed biopsies from the anterior horn should be included in extended biopsy prot
77 nce of abundant migratory neuroblasts in the anterior horn SVZ forming structures here denominated ce
78 ere performed of the ventricular index (VI), anterior horn width (AHW), and thalamo-occipital distanc
79 y significant differences with regard to the anterior horn width of the right and left lateral ventri
80 te matter hyperintensity dorsolateral to the anterior horns, with higher signal intensity than in the