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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.
4 glial activation and synaptic changes in the anterior horn (AH), respectively.
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
7 etween first and second motor neurons in the anterior horn at the lumbar level.
8 A) is a motor neuron disorder resulting from anterior horn cell death.
9 non-immune forms of PNH that include toxins, anterior horn cell degeneration in motor neurone disease
10  tract but persists in the face of selective anterior horn cell destruction.
11 re syndrome 1 and lethal arthrogryposis with anterior horn cell disease are autosomal recessive fetal
12 enerative conditions such as Alzheimer's and anterior horn cell disease.
13 41 million (95% CI, $1132-$1351 million) for anterior horn cell disease; $75 million (95% CI, $57-$92
14            Spinal cord had axonal spheroids, anterior horn cell loss and axonal degeneration in anter
15 oma-spinal cord-34 motor neurons and primary anterior horn cell neurons showed that IL-6 exerted a ne
16 is virus (TMEV) cleared virus infection from anterior horn cell neurons.
17 ot accompanied by significant axonal loss or anterior horn cell pathology.
18 eased myofiber size and number and increased anterior horn cell size.
19                  The motor unit includes the anterior horn cell, the motor axon and the muscle fibers
20 he distal motor nerve up to the level of the anterior horn cell.
21 of the central grey matter, with predominant anterior horn-cell involvement, and nine (75%) children
22 A) is a motor-neuron disorder resulting from anterior-horn-cell death.
23 udy is to investigate the involvement of the anterior horn cells (AHC) in the early post-stroke perio
24 s suggested the possibility of impairment of anterior horn cells (AHC-s).
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.
27 ized by specific degeneration of spinal cord anterior horn cells and subsequent muscle atrophy.
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
30 Virus antigen was localized predominantly to anterior horn cells in infected IL-6-/- H-2q mice.
31                          There was a loss of anterior horn cells in the spinal cord.
32 ly less affected neuronal subpopulation, the anterior horn cells of the spinal cord.
33 and paralysis as a result of degeneration of anterior horn cells of the spinal cord.
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
36  corticospinal tract, without involvement of anterior horn cells.
37 s and nuclei and in the neuropil surrounding anterior horn cells.
38 iquitin-positive intraneuronal aggregates in anterior horn cells.
39 ron" pattern: a symmetric involvement of the anterior horn cells.
40 7% in Purkinje cells to 80.6 +/- 2.8% in the anterior horn cells.
41 erebral and brainstem neurons to spinal cord anterior horn cells; thus, severe poliomyelitis, but not
42                               Maximal medial anterior horn displacement occurred in 60 degrees of fle
43                                       In the anterior horn enriched mRNA pool, we could not clearly i
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
46 oplasmic Lewy body-like inclusions in spinal anterior horn motor neurons.
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
55              Arthroscopic examination of the anterior horn of the lateral meniscus in all 22 patients
56 d speckled increased signal intensity at the anterior horn of the lateral meniscus near its central a
57            Increased signal intensity at the anterior horn of the lateral meniscus near its central a
58            Increased signal intensity at the anterior horn of the lateral meniscus was seen on the im
59 teoarthritis was induced by resection of the anterior horn of the medial meniscus and of the medial c
60                    Some motor neurons in the anterior horn of the spinal cord also were immunopositiv
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
66                                       In the anterior horn of the spinal cord, virtually all motor ne
67 pathy with prominent vacuolar changes in the anterior horn of the spinal cord.
68 generation of the alpha-motor neurons in the anterior horn of the spinal cord.
69 proteins selectively in motor neurons of the anterior horn of the spinal cord.
70                               Neurons in the anterior horn of the spinal cords of paralyzed mice exhi
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
76     The Lamin B2 signature also presented in anterior horn, spinal cord neurons from post-mortem ALS
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