{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,21]],"date-time":"2026-10-21T12:42:54Z","timestamp":1792586574405,"version":"4.5.0"},"reference-count":20,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2026,1,1]],"date-time":"2026-01-01T00:00:00Z","timestamp":1767225600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2026,1,1]],"date-time":"2026-01-01T00:00:00Z","timestamp":1767225600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2026,8,24]],"date-time":"2026-08-24T00:00:00Z","timestamp":1787529600000},"content-version":"vor","delay-in-days":235,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Clinical Neurophysiology Practice"],"published-print":{"date-parts":[[2026]]},"DOI":"10.1016\/j.cnp.2026.08.010","type":"journal-article","created":{"date-parts":[[2026,8,25]],"date-time":"2026-08-25T15:08:52Z","timestamp":1787670532000},"page":"749-756","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":0,"special_numbering":"C","title":["Impaired motor unit profile in Fabry disease: A quantitative electrophysiological study"],"prefix":"10.1016","volume":"11","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-2365-0850","authenticated-orcid":false,"given":"Aysegul","family":"Gunduz","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Aysegul","family":"Akkan Suzan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mevl\u00fct Tamer","family":"Din\u00e7er","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"\u015eeyda G\u00fcl","family":"\u00d6zcan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nurhan","family":"Seyahi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.cnp.2026.08.010_bb0005","doi-asserted-by":"crossref","first-page":"147","DOI":"10.1016\/S0304-3959(00)00482-6","article-title":"The LANSS pain scale: the Leeds assessment of neuropathic symptoms and signs","volume":"92","author":"Bennett","year":"2001","journal-title":"Pain"},{"key":"10.1016\/j.cnp.2026.08.010_bb0010","doi-asserted-by":"crossref","first-page":"963","DOI":"10.54029\/2022pvi","article-title":"Sympathetic skin response, cutaneous silent period and nociceptive flexion reflex in Fabry disease","volume":"27","author":"Boluk","year":"2022","journal-title":"Neurology Asia"},{"key":"10.1016\/j.cnp.2026.08.010_bb0015","doi-asserted-by":"crossref","first-page":"2048","DOI":"10.2337\/diacare.25.11.2048","article-title":"Validation of the Toronto clinical scoring system for diabetic polyneuropathy","volume":"25","author":"Bril","year":"2002","journal-title":"Diabetes Care"},{"key":"10.1016\/j.cnp.2026.08.010_bb0020","doi-asserted-by":"crossref","first-page":"240","DOI":"10.1111\/j.1464-5491.2009.02667.x","article-title":"Reliability and validity of the modified Toronto clinical neuropathy score in diabetic sensorimotor polyneuropathy","volume":"26","author":"Bril","year":"2009","journal-title":"Diabet. Med."},{"key":"10.1016\/j.cnp.2026.08.010_bb0025","first-page":"4","article-title":"A review of Fabry disease","volume":"23","author":"Chan","year":"2018","journal-title":"Skin Therapy Lett."},{"key":"10.1016\/j.cnp.2026.08.010_bb0030","doi-asserted-by":"crossref","first-page":"2979","DOI":"10.1016\/j.clinph.2016.06.011","article-title":"MUNIX: reproducibility and clinical correlations in amyotrophic lateral sclerosis","volume":"127","author":"Escorcio-Bezerra","year":"2016","journal-title":"Clin. Neurophysiol."},{"key":"10.1016\/j.cnp.2026.08.010_bb0035","doi-asserted-by":"crossref","first-page":"360","DOI":"10.1111\/j.1399-0004.1988.tb03463.x","article-title":"Enzyme replacement in Fabry endothelial cells and fibroblasts: uptake experiments and electron microscopical studies","volume":"33","author":"Hasholt","year":"1988","journal-title":"Clin. Genet."},{"key":"10.1016\/j.cnp.2026.08.010_bb0040","doi-asserted-by":"crossref","first-page":"2481","DOI":"10.1111\/ene.15870","article-title":"Optimal cut-off value of the modified Toronto clinical neuropathy score in the diagnosis of polyneuropathy","volume":"30","author":"Idiaquez","year":"2023","journal-title":"Eur. J. Neurol."},{"key":"10.1016\/j.cnp.2026.08.010_bb0045","series-title":"Electrodiagnosis in Diseases of Nerve and Muscle. Principles and practice","author":"Kimura","year":"2006"},{"key":"10.1016\/j.cnp.2026.08.010_bb0050","doi-asserted-by":"crossref","first-page":"1107","DOI":"10.1111\/j.1526-4637.2010.00837.x","article-title":"Validity and reliability of the Turkish self-administered Leeds assessment of neuropathic symptoms and signs (S-LANSS) questionnaire","volume":"11","author":"Koc","year":"2010","journal-title":"Pain Med."},{"issue":"1","key":"10.1016\/j.cnp.2026.08.010_bb0055","doi-asserted-by":"crossref","first-page":"6267","DOI":"10.1038\/s41598-026-37198-3","article-title":"Characteristics of motor polyneuropathy in Fabry disease: a case-control study","volume":"16","author":"Koszewicz","year":"2026","journal-title":"Sci. Rep."},{"key":"10.1016\/j.cnp.2026.08.010_bb0060","doi-asserted-by":"crossref","DOI":"10.1016\/j.cca.2024.119824","article-title":"LysoGb3 quantification facilitates phenotypic categorization of Fabry disease patients: insights gained by a novel MS\/MS method","volume":"561","author":"Kuchar","year":"2024","journal-title":"Clin. Chim. Acta"},{"key":"10.1016\/j.cnp.2026.08.010_bb0065","first-page":"602","article-title":"Endocytosis of lysosomal alpha-galactosidase a by cultured fibroblasts from patients with Fabry disease","volume":"34","author":"Mayes","year":"1982","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.cnp.2026.08.010_bb0070","doi-asserted-by":"crossref","first-page":"641","DOI":"10.1016\/j.amjms.2020.07.011","article-title":"When and how to diagnose Fabry disease in clinical practice","volume":"360","author":"Michaud","year":"2020","journal-title":"Am. J. Med. Sci."},{"key":"10.1016\/j.cnp.2026.08.010_bb0075","first-page":"2209","article-title":"Motor unit number index (MUNIX)","volume":"51","author":"Nandedkar","year":"2004","journal-title":"I.E.E.E. Trans. Biomed. Eng."},{"key":"10.1016\/j.cnp.2026.08.010_bb0080","doi-asserted-by":"crossref","first-page":"798","DOI":"10.1002\/mus.21824","article-title":"Motor unit number index (MUNIX): principle, method, and findings in healthy subjects and in patients with motor neuron disease","volume":"42","author":"Nandedkar","year":"2010","journal-title":"Muscle Nerve"},{"issue":"3","key":"10.1016\/j.cnp.2026.08.010_bb0085","doi-asserted-by":"crossref","first-page":"374","DOI":"10.1002\/mus.26099","article-title":"Motor unit number index: guidelines for recording signals and their analysis","volume":"58","author":"Nandedkar","year":"2018","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.cnp.2026.08.010_bb0090","doi-asserted-by":"crossref","first-page":"1172","DOI":"10.1136\/jnnp-2015-310509","article-title":"Tracking motor neuron loss in a set of six muscles in amyotrophic lateral sclerosis using the motor unit number index (MUNIX): a 15-month longitudinal multicentre trial","volume":"86","author":"Neuwirth","year":"2015","journal-title":"J. Neurol. Neurosurg. Psychiatry"},{"key":"10.1016\/j.cnp.2026.08.010_bb0095","doi-asserted-by":"crossref","first-page":"1249","DOI":"10.1212\/WNL.52.6.1249","article-title":"Quantitative analysis of epidermal innervation in Fabry disease","volume":"52","author":"Scott","year":"1999","journal-title":"Neurology"},{"key":"10.1016\/j.cnp.2026.08.010_bb0100","doi-asserted-by":"crossref","first-page":"548","DOI":"10.1002\/mus.20390","article-title":"Evidence for motor axon depolarization in Fabry disease","volume":"32","author":"Tan","year":"2005","journal-title":"Muscle Nerve"}],"container-title":["Clinical Neurophysiology Practice"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2467981X26000843?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2467981X26000843?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2026,10,21]],"date-time":"2026-10-21T12:01:35Z","timestamp":1792584095000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S2467981X26000843"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026]]},"references-count":20,"alternative-id":["S2467981X26000843"],"URL":"https:\/\/doi.org\/10.1016\/j.cnp.2026.08.010","relation":{},"ISSN":["2467-981X"],"issn-type":[{"value":"2467-981X","type":"print"}],"subject":[],"published":{"date-parts":[[2026]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Impaired motor unit profile in Fabry disease: A quantitative electrophysiological study","name":"articletitle","label":"Article Title"},{"value":"Clinical Neurophysiology Practice","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.cnp.2026.08.010","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2026 The Authors. Published by Elsevier B.V. on behalf of International Federation of Clinical Neurophysiology.","name":"copyright","label":"Copyright"}]}}