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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 uch, and proprioceptive sensing) in multiple dermatomes.
9 ly in mesenchyme-derived cell types: (1) the dermatome and limb bud mesenchyme and, later, the subder
10 Chick ADAM 10 is expressed in the developing dermatome and myotome of the somite, epidermis, gut endo
11 nerves (n = 37); (2) pain in the trigeminal dermatomes and any combination involving the spinal derm
13 nnervate characteristic skin regions, termed dermatomes, and their axons project somatotopically in t
14 mes and any combination involving the spinal dermatomes C2, C3, and C4, but no other dermatomes (n =
16 loss of the receptor from all sclerotome and dermatome derivatives or disruption of PDGFRalpha-driven
18 of sensory function (to normal limits in all dermatomes for at least one modality in 16 out of 20 ope
19 In vitro skin permeation was performed in dermatomed human skin and HPLC was used to analyze the d
20 tomes (n = 32); and (3) pain sites involving dermatomes in addition to the ones listed above (n = 131
21 tes, SlF mRNA expression by the cells of the dermatome is normal in Ph embryos when neural crest-deri
22 eservation of sensory function in the T11-L2 dermatomes is associated with psychogenically mediated g
23 urography) and red cell flux in the affected dermatome (laser Doppler flowmetry; dorsum of foot) were
24 sensory neurons from the rat in vivo spared dermatome model of collateral sprouting identified the a
25 inal dermatomes C2, C3, and C4, but no other dermatomes (n = 32); and (3) pain sites involving dermat
26 of restored sensation in avulsed spinal root dermatomes, now presumably routed via nerves that had be
28 l tissue, dorsal mesenchyme derived from the dermatome region of the somites, the brachial arches, an
29 istribution according to the arrangements of dermatomes revealed three distinct clusters of patients:
31 by cutaneous neurogenic inflammation, in the dermatome that overlaps with visceral afferent innervati
32 ridization shows that c-Krox is expressed in dermatomes, the somite derivatives that generate dermis,
33 -positive dermomyotome enter the myotome and dermatome, thereby superimposing the En1-Sim1 expression
36 .7 is increased in human DRG neurons only in dermatomes where patients are experiencing acquired neur
38 he somatotopic representation of the footpad dermatome within the dorsal root ganglia and spinal cord
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