{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,10]],"date-time":"2025-09-10T22:48:09Z","timestamp":1757544489537},"reference-count":30,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2004,10,7]],"date-time":"2004-10-07T00:00:00Z","timestamp":1097107200000},"content-version":"vor","delay-in-days":8042,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Annals of Neurology"],"published-print":{"date-parts":[[1982,10]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Peripheral and central nerve conduction were studied in five patients who had polyneuropathy associated with pigmentation, hypertrichosis, edema, and plasma cell dycrasia by using the short\u2010latency somatosensory evoked potential (SEP) to electrical stimulation of the median nerve at the wrist. The clavicular component <jats:styled-content>N9<\/jats:styled-content> was markedly reduced inamplitude, and its latency was moderately prolonged. The interpeak latency from <jats:styled-content>N9<\/jats:styled-content> to the cervical component <jats:styled-content>N13<\/jats:styled-content> was significantly prolonged, indicating a conduction delay in the dorsal root. The interpeak latency from <jats:styled-content>N13<\/jats:styled-content> to the cortical component <jats:styled-content>N20<\/jats:styled-content> was normal, suggesting normal central conduction. These Physiological findings were consistent with the pathological findings, which showed degeneration of axons and segmental demyelination and remyelination in the sural nerve and extensive segmental demyelination and remyelination in the dorsal root but normal posterior columns of the spina cord. SEP is a noninvasive method of localizing the site of axon or myelin disorder in a peripheral neuropathy.<\/jats:p>","DOI":"10.1002\/ana.410120407","type":"journal-article","created":{"date-parts":[[2005,1,1]],"date-time":"2005-01-01T13:35:08Z","timestamp":1104586508000},"page":"355-360","source":"Crossref","is-referenced-by-count":15,"title":["Use of SEPs to localize degeneration in a rare polyneuropathy: Studies on polyneuropathy associated with pigmentation, hypertrichosis, edema, and plasma cell 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