ライフサイエンスコーパス: dermatome

1 ance of vesicular rash on the foot in the L4 dermatome.

2 us stimulation of the ipsilateral ophthalmic dermatome.

3 red thermal sensitivity in the same affected dermatomes.

4 in both injured and adjacent uninjured (L4) dermatomes.

5 ed by stimulation in cervical but not lumbar dermatomes.

6 mal stimulation in either lumbar or cervical dermatomes.

7 rger zosteriform skin lesions along affected dermatomes.

8 uch, and proprioceptive sensing) in multiple dermatomes.

9 stimulation on the skin surface in the PFCN dermatome also inhibited bladder activity.

10 ly in mesenchyme-derived cell types: (1) the dermatome and limb bud mesenchyme and, later, the subder

11 Chick ADAM 10 is expressed in the developing dermatome and myotome of the somite, epidermis, gut endo

12 nerves (n = 37); (2) pain in the trigeminal dermatomes and any combination involving the spinal derm

13 novel skin regions, and mapped the resulting dermatomes and central projections.

14 44-1.01) and C8 (OR, 036; 95% CI, 0.24-0.53) dermatomes, and motor scores of the elbow flexors (C5) (

15 nnervate characteristic skin regions, termed dermatomes, and their axons project somatotopically in t

16 mes and any combination involving the spinal dermatomes C2, C3, and C4, but no other dermatomes (n =

17 e spinal cord at the level of the stimulated dermatomes C5/C6.

18 loss of the receptor from all sclerotome and dermatome derivatives or disruption of PDGFRalpha-driven

19 (laser-Doppler flowmetry) in the innervated dermatome (dorsum of foot) were continuously measured.

20 ary for VZV transfer to skin in the affected dermatome during herpes zoster.

21 of sensory function (to normal limits in all dermatomes for at least one modality in 16 out of 20 ope

22 In vitro skin permeation was performed in dermatomed human skin and HPLC was used to analyze the d

23 using an in vitro permeation test (IVPT) and dermatomed human skin, and in vivo in human pharmacokine

24 tomes (n = 32); and (3) pain sites involving dermatomes in addition to the ones listed above (n = 131

25 ve monkeys, and in ganglia from at least two dermatomes in three of five monkeys.

26 tes, SlF mRNA expression by the cells of the dermatome is normal in Ph embryos when neural crest-deri

27 eservation of sensory function in the T11-L2 dermatomes is associated with psychogenically mediated g

28 urography) and red cell flux in the affected dermatome (laser Doppler flowmetry; dorsum of foot) were

29 sensory neurons from the rat in vivo spared dermatome model of collateral sprouting identified the a

30 inal dermatomes C2, C3, and C4, but no other dermatomes (n = 32); and (3) pain sites involving dermat

31 of restored sensation in avulsed spinal root dermatomes, now presumably routed via nerves that had be

32 /112) of patients the site of EM matched the dermatomes of radicular pain.

33 from fewer DRGs than normal, but the overall dermatome pattern was preserved.

34 l tissue, dorsal mesenchyme derived from the dermatome region of the somites, the brachial arches, an

35 istribution according to the arrangements of dermatomes revealed three distinct clusters of patients:

36 NP2 was injected intradermally into the dermatome(s) corresponding to the radicular distribution

37 by cutaneous neurogenic inflammation, in the dermatome that overlaps with visceral afferent innervati

38 ridization shows that c-Krox is expressed in dermatomes, the somite derivatives that generate dermis,

39 -positive dermomyotome enter the myotome and dermatome, thereby superimposing the En1-Sim1 expression

40 The period prevalence of HZ in any dermatome was 1.1%, the frequency of HZ involving V1 (HZ

41 us heat applied to either cervical or lumbar dermatomes was studied in awake rats.

42 .7 is increased in human DRG neurons only in dermatomes where patients are experiencing acquired neur

43 growth region and from which the mesenchymal dermatome will later emerge.

44 he somatotopic representation of the footpad dermatome within the dorsal root ganglia and spinal cord

45 tial characteristics associated with painful dermatomes within minutes of treatment.