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17篇 您的检索式:作者名="Nolano"
    题名 作者 年代 出处 被引量
1Sensory deficit in Parkinson's disease:evidence of a cutaneous denervation 显示文摘NOLANO M PROVITERA V ESTRANEO A 2008Brain2008,131,:1
2Quantification of myelinated endings and mechanoreceptors in human digital skin显示文摘Nolano M Provitera V Crisci C 2003Ann Neurol2003,54,:1
3Evaluation of sudonotor function in diabetes using the dynamic sweat test显示文摘Provitera V Nolano M Caporaso G 0,,:1
4Topical capsaicin in humans : parallel loss of epidermal nerve fibers and pain sensation显示文摘NOLANO M SIMONE DA WENDELSCHAFER-CRABB G 1999Pain1999,81,12:1
5Mutilating fingertip ulcers in uncontrolled type 1 diabetes mellitus显示文摘Raffaele Dubbioso Maria Nolano Raffaella Mazzarella Angela Albarosa Rivellese Fiore Manganelli 2014Neurological Sciences2014,,1:1
6Quantification of pilomotor nerves:a new tool to evaluate autonomic involvement in diabetes显示文摘Nolano M Provitera V Caporaso G 0,,:1
7Small fiber involvement in Fried- reichs ataxia显示文摘Nolano M Provitera V Crisci C 2001Ann Neurol2001,50,:1
8Quantification of myelinated endings and mechanoreceptors in human digital skin显示文摘Nolano M Provitera V Crisci C 2003Ann Neurol2003,54,:1
9Blockade of glutamate mGlu5 receptors in a rat model of neuropathic pain prevents early over-expression of pro-apoptotic genes and morphological changes in dorsal horn lamina II显示文摘Vito de Novellis Dario Siniscalco Umberto Galderisi Carlo Fuccio Maria Nolano Lucio Santoro Antonino Cascino Kevin A. Roth Francesco Rossi Sabatino Maione 2003Neuropharmacology2003,,4:1
10Autoimmune auto- nomic ganglionopathy: a possible postganglionic neuropathy显示文摘Manganelli F Dubbioso R Nolano M 2011Arch Neurol2011,68,:1
11Ross syndrome: a rare or a misknown disorder of thermoregulation? A skin innervation study on 12 subjects显示文摘Nolano M Provitera V Perretti A 2006Brain2006,129,8:1
12Ross syndrome: a rare or a misknown disorder of thermoregulation? A skin innervation study on 12 subjects显示文摘Nolano M Provitera V Perretti A 2006Brain2006,129,:1
13Sensory deficit in Parkinson,s disease:evidence of a cutaneous denervation显示文摘Nolano M Provitera V Estraneo A 2008Brain2008,131,7:1
14Topical capsaicin in humans: parallel loss of epidermal nerve fibers and pain sensation显示文摘Nolano M Simone D A Wendelschafer-Crabb G 1999Pain1999,81,:1
15Top- ical capsaicin in humans: parallel loss of epidermal nerve fibers and pain sensation显示文摘Nolano M Simone DA Wendelschafer-Crabb G 1999Pain1999,81,12:1
16Topical capsaicin in humans: parallel loss of epidermal nerve fibers and pain sensation显示文摘Nolano M Simone DA Wendelschafer-Crabb G 1999Pain1999,81,12:1
17Ross综合征是否为一种罕见且常被误解的体温调节障碍疾病:12例患者皮肤神经支配研究显示文摘Ross syndrome is described as a rare disorder of sweating associated with areflexia and tonic pupil. Since Ross’s first description in 1958, ~40 cases have been described. We assessed the involvement of cutaneous innervation in 12 subjects with Ross syndrome using quantitative sensory testing, sweating assessment and immunohistochemical study of anhidrotic and hyperhidrotic skin. This evaluation was repeated over time in 4 out of 12 subjects. In addition, we enrolled four subjects with Holmes-Adie syndrome (areflexia and tonic pupil)to investigate similarities between the two conditions. We found in Ross patients a complex and progressive involvement of cutaneous sensory and autonomic innervation underlying the impairment of heat production and heat dissipation through both loss of sweating and loss of cutaneous blood flow regulation. In Holmes-Adie subjects we found a mild impairment of sweating without thermoregulatory problems. The persistence of a sudomotor vasoactive intestinal peptide-immunoreactive (VIP-ir) innervation, although deranged and poor, definitely differentiated Holmes-Adie from Ross patients. Ross syndrome is a progressive and complex disorder of thermoregulation difficult to differentiate from the probably pathogenetically related Holmes-Adie syndrome. Sweating assessment and skin biopsy are suitable tools to define a boundary between them. Owing to the large number of Ross patients observed in only 5 years, and to the long and complex medical history of most of them, doubts arise on the effective rarity of this condition, and we warn family doctors and other specialists, besides neurologists, to become aware of this complex disorder.Nolano M. Provitera V. Perretti A. 张磊 2006世界核心医学期刊文摘(眼科学分册)2006,2,12:0
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