{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,18]],"date-time":"2025-10-18T10:18:04Z","timestamp":1760782684783},"reference-count":9,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2004,10,8]],"date-time":"2004-10-08T00:00:00Z","timestamp":1097193600000},"content-version":"vor","delay-in-days":4390,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Annals of Neurology"],"published-print":{"date-parts":[[1992,10]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>We report on 3 siblings with an adult\u2010onset, predominantly distal muscle weakness. In the female index patient this was associated with epilepsy and a progressive spastic ataxic gait, while the 2 other siblings had no appreciable clinical nervous system involvement. Additional investigations revealed muscular dystrophy and leukoencephalopathy in all 3 siblings. We conclude that this familial adult\u2010onset muscular dystrophy associated with leukoencephalopathy represents a newly recognized autosomal recessive syndrome.<\/jats:p>","DOI":"10.1002\/ana.410320415","type":"journal-article","created":{"date-parts":[[2005,1,1]],"date-time":"2005-01-01T12:16:16Z","timestamp":1104581776000},"page":"577-580","source":"Crossref","is-referenced-by-count":8,"title":["Familial adult\u2010onset muscular dystrophy with leukoencephalopathy"],"prefix":"10.1002","volume":"32","author":[{"given":"Baziel G. M.","family":"van Engelen","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Quint H.","family":"Leyten","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Pieter L. J. 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