{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,9]],"date-time":"2026-04-09T14:00:12Z","timestamp":1775743212299,"version":"3.50.1"},"reference-count":19,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2002,2,19]],"date-time":"2002-02-19T00:00:00Z","timestamp":1014076800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Muscle and Nerve"],"published-print":{"date-parts":[[2002,4]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Myotonic dystrophy type 1 (DM1) is the most common inherited muscle disorder and may present in numerous ways due to characteristic multisystem involvement. We report a 47\u2010year\u2010old man who presented with an 8\u2010year history of slowly progressive dyspnea and episodic stridor. The laryngeal paresis was documented with videostroboscopy and laryngeal electromyography, and treated with tracheostomy and antimyotonia agents. \u00a9 2002 Wiley Periodicals, Inc. Muscle Nerve 25: 000\u2013000, 2002<\/jats:p>","DOI":"10.1002\/mus.10062","type":"journal-article","created":{"date-parts":[[2002,8,25]],"date-time":"2002-08-25T23:15:07Z","timestamp":1030317307000},"page":"616-618","source":"Crossref","is-referenced-by-count":10,"title":["Myotonic dystrophy type 1 (DM1) presenting with laryngeal stridor and vocal fold paresis"],"prefix":"10.1002","volume":"25","author":[{"given":"Jennifer L.","family":"Ahmadian","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Scott L.","family":"Heller","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Takashi","family":"Nishida","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kenneth W.","family":"Altman","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2002,3,25]]},"reference":[{"key":"e_1_2_5_2_2","first-page":"13","article-title":"Dystrophia myotonica und syringomyelie","volume":"26","author":"Acvenarius HJ","year":"1968","journal-title":"Wien Z Nervenheilkd Grenzgeb"},{"key":"e_1_2_5_3_2","doi-asserted-by":"publisher","DOI":"10.1148\/92.1.104"},{"key":"e_1_2_5_4_2","first-page":"155","article-title":"A propos de deux cas peu banals d'electro\u2010myographia laryngee","volume":"12","author":"DeJonckere P","year":"1975","journal-title":"Rev Electrodiagn Ther"},{"key":"e_1_2_5_5_2","doi-asserted-by":"publisher","DOI":"10.1136\/jnnp.51.11.1461-a"},{"key":"e_1_2_5_6_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0030-6665(20)31418-3"},{"key":"e_1_2_5_7_2","doi-asserted-by":"publisher","DOI":"10.1136\/thx.51.1.108"},{"key":"e_1_2_5_8_2","volume-title":"Myotonic dystrophy","author":"Harper PS","year":"1989"},{"key":"e_1_2_5_9_2","doi-asserted-by":"publisher","DOI":"10.1053\/hn.1999.v121.a98733"},{"key":"e_1_2_5_10_2","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.54.6.1218"},{"key":"e_1_2_5_11_2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1600-0404.1992.tb05103.x"},{"key":"e_1_2_5_12_2","doi-asserted-by":"publisher","DOI":"10.1001\/archotol.1976.00780080107016"},{"key":"e_1_2_5_13_2","doi-asserted-by":"publisher","DOI":"10.1126\/science.1546325"},{"key":"e_1_2_5_14_2","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.40.5.839"},{"key":"e_1_2_5_15_2","doi-asserted-by":"publisher","DOI":"10.1002\/1097-4598(200012)23:12<1789::AID-MUS2>3.0.CO;2-4"},{"issue":"1","key":"e_1_2_5_16_2","first-page":"1","article-title":"Manifestazioni faringo\u2010laringee nella miastenia (M. di Erb\u2010Goldflam) e nella distrofia miotonica (M. 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