ライフサイエンスコーパス: rhizotomy

1 2) diminishing their input by dorsal rootlet rhizotomy.

2 (short term) or 16-32 weeks (long term) post-rhizotomy.

3 ration persisted at least 10 d after ventral rhizotomy.

4 ession and also decreased dramatically after rhizotomy.

5 pressed on sprouting axons following chronic rhizotomy.

6 ation following a unilateral cervical dorsal rhizotomy.

7 d by immunocytochemistry staining and dorsal rhizotomy.

8 id receptors that was maximal at 8 days post-rhizotomy.

9 n 24 hr after sciatic nerve injury or dorsal rhizotomy.

10 fferents and neurons denervated after dorsal rhizotomy.

11 orsal horn 6-8 weeks after a cervical dorsal rhizotomy.

12 nd 30 days following complete retrogasserian rhizotomy.

13 ation of pain in humans following trigeminal rhizotomy.

14 eters were analyzed before and following the rhizotomy: 1) percentage of successful retrievals; 2) di

15 Three days after L4/5 ventral rhizotomy, [3H]thymidine incorporation into Remak Schwan

16 However, because dorsal rhizotomy abolishes VR1 staining in both laminae I and I

17 ive capacity of sensory neurons after dorsal rhizotomy, allowing regeneration across the dorsal root

18 sensory profiles (which did not occur after rhizotomy alone), as well as regeneration of cholera tox

19 control spasticity, such as selective dorsal rhizotomy and administration of botulinum toxin or intra

20 st VGLUT1 immunoreactivity disappeared after rhizotomy and colocalized with markers of cutaneous (SSE

21 ment were assessed 2, 4, 8, and 16 days post rhizotomy and compared with those of untreated rats.

22 injury paradigms, cervical multilevel dorsal rhizotomy and midthoracic dorsal spinal cord hemisection

23 uding dorsal column transection, dorsal root rhizotomy and peripheral axotomy.

24 ir fibers, which was strongest 10 days after rhizotomy and weaker at 30 days, which was still stronge

25 and CGRP identify sprouting axons following rhizotomy, and that exercise does not upregulate L1 expr

26 ridine (BrdU) injections 2-3 weeks after the rhizotomy, and were perfused 4-6 weeks later.

27 ng of the sciatic nerve or unilateral dorsal rhizotomy at lumbar levels L4/5, and bilateral dorsal fu

28 al thresholds was observed after the ventral rhizotomy but not after the sham operation.

29 DREZ, which begins almost immediately after rhizotomy, but with the delayed appearance of mature ED1

30 Cervical dorsal rhizotomy (CDR) enhances serotonin terminal density near

31 the subdiaphragmatic vagus using unilateral rhizotomy combined with contralateral subdiaphragmatic v

32 sprouting of primary afferents spared by the rhizotomy could mediate this cortical reactivation.

33 ously shown that following a cervical dorsal rhizotomy, CST projections originating from primary soma

34 PSC amplitudes and was abolished by a dorsal rhizotomy, demonstrating that capsaicin acts via presyna

35 Dorsal rhizotomy diminished basal level expression and blocked

36 Moreover, an L5 dorsal root rhizotomy does not reverse this pain behavior, suggestin

37 Unilateral dorsal rhizotomy eliminated the characteristic pattern of TNFR1

38 ast to the decrease seen in the nuclei after rhizotomy, examination of the central root that was stil

39 Rhizotomy experiments and ultrastructural observations i

40 In adult monkeys with dorsal rhizotomies extending from the second cervical (C2) to t

41 jected to cervical and upper thoracic dorsal rhizotomies for 13-21 years and that had shown extensive

42 L1 expression by giving animals with chronic rhizotomies free access to an exercise wheel.

43 d drugs (baclofen), and surgery (neurectomy, rhizotomy) has become more frequent.

44 we investigated the effects of an L5 ventral rhizotomy in rat.

45 -1 subunit expression with or without dorsal rhizotomy in spinal nerve-ligated rats and its correlati

46 y axon regeneration is observed after dorsal rhizotomy in transgenic mice.

47 ilateral sciatic nerve crush, but not dorsal rhizotomy, indicating a peripheral origin of the express

48 Rhizotomy induced a dramatic increase in CGRP-IR within

49 Rhizotomy induced approximately a 50% ipsilateral loss i

50 Dorsal rhizotomies ipsilateral to the nerve injury in neuropath

51 In contrast, dorsal rootlet rhizotomy led to a significant increase in corticospinal

52 tically in peripheral nerve after L5 ventral rhizotomy; many of these were macrophage nuclei.

53 Following rhizotomy, most, but not all, of the CGRP-IR was lost fr

54 ficits observed in control mice after dorsal rhizotomy, neuron-specific Nf1 mutant mice spontaneously

55 contrast to previous studies, neither dorsal rhizotomy nor an intrathecal injection of capsaicin, whi

56 diography using [125I]BIM 23027 after dorsal rhizotomy of the lumbar dorsal roots, L4 and L5, suggest

57 and fifth lumbar ventral roots (L4/5 ventral rhizotomy) of the rat is highly selective, sparing unmye

58 -IR in the n. gracilis was blocked by dorsal rhizotomy or dorsal column lesion.

59 c nerve lesioning (P < 0.001), but not after rhizotomy or dorsal funiculus lesioning.

60 Previously, we observed that, after dorsal rhizotomy, overexpression of NGF leads to robust regener

61 reorganization that occurs following dorsal rhizotomy plays a key role in the recovery of hand funct

62 fferent) vagal fibers by making a unilateral rhizotomy plus contralateral subdiaphragmatic vagotomy.

63 We found that L4/5 ventral rhizotomy prompted many normally innervated nonmyelinati

64 Dorsal rhizotomy reduced, but did not eliminate, the immunostai

65 Seven days after L5 ventral rhizotomy, Remak Schwann cells in the L5-predominant lat

66 II, the effects of bilateral L6 dorsal root rhizotomy (RH) combined with unilateral (UPx) or bilater

67 Unilateral dorsal rhizotomy significantly reduced AT(1) receptor binding i

68 VGLUT2 immunoreactivity did not change after rhizotomy, suggesting a preferential intrinsic origin.

69 stained puncta disappear 4 days after dorsal rhizotomy, suggesting that most of GluR5/6/7-immunoposit

70 l dorsal horn by performing acute unilateral rhizotomies (T12-L4) in adult rats.

71 Immediately following a dorsal rhizotomy that removes input from the thumb, index, and

72 of rats that had received unilateral ventral rhizotomies to eliminate efferents.

73 An extensive unilateral dorsal rhizotomy was performed across seven or eight successive

74 L6-S1 ganglionectomies or L6-S1 ventral root rhizotomies we limited viral transport to the sympatheti

75 adult rats with comparably extensive dorsal rhizotomies, we employed anatomical tracing techniques t

76 ogenous cortical neurogenesis after a dorsal rhizotomy, which may play a role in functional recovery.

77 After rhizotomy with immediate NT-3 treatment, regeneration co