{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,7]],"date-time":"2026-07-07T14:16:30Z","timestamp":1783433790017,"version":"3.54.6"},"reference-count":32,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2026,6,24]],"date-time":"2026-06-24T00:00:00Z","timestamp":1782259200000},"content-version":"vor","delay-in-days":23,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,6,1]],"date-time":"2026-06-01T00:00:00Z","timestamp":1780272000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Euro J of Neurology"],"published-print":{"date-parts":[[2026,6]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Whether serial electrophysiology may be useful in chronic inflammatory demyelinating polyneuropathy (CIDP), in remission off treatment, is unknown.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>We retrospectively studied electrophysiological findings during active disease and post\u2010remission, in subjects with CIDP, at 2 UK neuropathy centres.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      We included 24 consecutive subjects. Eighteen (75%) had typical CIDP, 3 (12.5%) motor CIDP and 3 (12.5%) distal CIDP. Mean age was 61.3\u2009years (SD: 15.8). Mean interval between electrophysiological study during active disease and post\u2010remission was 63.25\u2009months (SD: 52.0). Mean distal motor latency improved for median (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u20090.001), ulnar (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u20090.001), fibular (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.01) and tibial (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.002) nerves. Mean motor conduction velocity improved for median (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u20090.001), ulnar (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u20090.001) and fibular (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.012) nerves. Mean minimum F\u2010wave latency improved for median (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.003), ulnar (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.002), and tibial (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.027) nerves. The proportion of nerves showing conduction block was greater during active disease than post\u2010remission (26\/66 vs. 10\/67;\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.002). Criteria for demyelination were initially fulfilled by all subjects, but not post\u2010remission (24\/24 vs. 14\/24;\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.006). Electrophysiological quasi\u2010normalisation correlated with shorter pre\u2010treatment disease duration (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.002). Amplitude of functional improvement correlated with fibular nerve motor amplitude at first study (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.024).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>Electrophysiological quasi\u2010normalisation may occur in a third of subjects with typical CIDP in clinical remission off treatment and may be more likely with prompt diagnosis\/treatment. Amelioration may be observed in all tested nerves. Initial fibular nerve motor amplitude may predict clinical improvement amplitude. The value of electrophysiology for prognostication\/disease monitoring\/management may merit further study in CIDP. Further research is warranted for subjects with variant and possible CIDP.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/ene.70670","type":"journal-article","created":{"date-parts":[[2026,6,24]],"date-time":"2026-06-24T10:42:04Z","timestamp":1782297724000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["The Electrophysiology of Disease Remission in Chronic Inflammatory Demyelinating Polyneuropathy"],"prefix":"10.1111","volume":"33","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-7170-8343","authenticated-orcid":false,"given":"Yusuf A.","family":"Rajabally","sequence":"first","affiliation":[{"name":"Aston Medical School, Aston University  Birmingham UK"},{"name":"Inflammatory Neuropathy Service, Department of Neurology University Hospitals Birmingham  Birmingham UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Joumana","family":"Freiha","sequence":"additional","affiliation":[{"name":"Wessex Neurological Centre, University Hospital Southampton  Southampton UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Roshan","family":"Iqbal","sequence":"additional","affiliation":[{"name":"Inflammatory Neuropathy Service, Department of Neurology University Hospitals Birmingham  Birmingham UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David","family":"Allen","sequence":"additional","affiliation":[{"name":"Wessex Neurological Centre, University Hospital Southampton  Southampton UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8245-0942","authenticated-orcid":false,"given":"Chinar","family":"Osman","sequence":"additional","affiliation":[{"name":"Wessex Neurological Centre, University Hospital Southampton  Southampton UK"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2026,6,24]]},"reference":[{"key":"e_1_2_9_2_1","doi-asserted-by":"publisher","DOI":"10.1002\/mus.23843"},{"key":"e_1_2_9_3_1","doi-asserted-by":"publisher","DOI":"10.1007\/s00415-018-9157-4"},{"key":"e_1_2_9_4_1","doi-asserted-by":"publisher","DOI":"10.1002\/mus.21733"},{"key":"e_1_2_9_5_1","doi-asserted-by":"publisher","DOI":"10.1002\/mus.24624"},{"key":"e_1_2_9_6_1","doi-asserted-by":"publisher","DOI":"10.1136\/jnnp-2013-306105"},{"key":"e_1_2_9_7_1","doi-asserted-by":"publisher","DOI":"10.1007\/s00415-017-8578-9"},{"key":"e_1_2_9_8_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.clinph.2020.10.008"},{"key":"e_1_2_9_9_1","doi-asserted-by":"publisher","DOI":"10.1212\/01.WNL.0000158680.89323.F8"},{"key":"e_1_2_9_10_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.clinph.2019.06.231"},{"key":"e_1_2_9_11_1","doi-asserted-by":"publisher","DOI":"10.1111\/ene.14959"},{"key":"e_1_2_9_12_1","doi-asserted-by":"publisher","DOI":"10.1136\/jnnp.2005.081547"},{"key":"e_1_2_9_13_1","first-page":"jnnp\u20102022\u201032963","article-title":"Application of the 2021 EAN\/PNS Criteria for Chronic Inflammatory Demyelinating Polyneuropathy","volume":"93","author":"Rajabally Y. 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