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Oral Motor Movements and Swallowing in Patients with Myotonic Dystrophy Type 1 (2013)

  • Authors:
  • USP affiliated authors: LIMONGI, SUELLY CECILIA OLIVAN - FM ; SASSI, FERNANDA CHIARION - FM ; ANDRADE, CLAUDIA REGINA FURQUIM DE - FM
  • USP Schools: FM; FM; FM
  • DOI: 10.1007/s00455-013-9458-9
  • Subjects: DEGLUTIÇÃO; MOTRICIDADE ORAL; MOVIMENTO (FISIOLOGIA); DISTROFIA MUSCULAR; TRANSTORNOS DE DEGLUTIÇÃO; ELETROMIOGRAFIA
  • Language: Inglês
  • Imprenta:
  • Source:
    • Título do periódico: Dysphagia
    • ISSN: 0179-051X
    • Volume/Número/Paginação/Ano: v. 28, n. 3, p. 446-454, 2013
  • Acesso online ao documento

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    Informações sobre o DOI: 10.1007/s00455-013-9458-9 (Fonte: oaDOI API)
    • Este periódico é de assinatura
    • Este artigo NÃO é de acesso aberto
    • Cor do Acesso Aberto: closed
    Versões disponíveis em Acesso Aberto do: 10.1007/s00455-013-9458-9 (Fonte: Unpaywall API)

    Título do periódico: Dysphagia

    ISSN: 0179-051X,1432-0460



      Não possui versão em Acesso aberto
    Informações sobre o Citescore
  • Título: Dysphagia

    ISSN: 0179-051X

    Citescore - 2017: 2

    SJR - 2017: 0.99

    SNIP - 2017: 1.416


  • Exemplares físicos disponíveis nas Bibliotecas da USP
    BibliotecaCód. de barrasNúm. de chamada
    FM2412005-10BCSEP 383 2013
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    • ABNT

      ERCOLIN, Beatriz; SASSI, Fernanda Chiarion; MANGILLI, Laura Davison; et al. Oral Motor Movements and Swallowing in Patients with Myotonic Dystrophy Type 1. Dysphagia, New York, v. 28, n. 3, p. 446-454, 2013. Disponível em: < http://link.springer.com/article/10.1007/s00455-013-9458-9 > DOI: 10.1007/s00455-013-9458-9.
    • APA

      Ercolin, B., Sassi, F. C., Mangilli, L. D., Mendonça, L. I. Z., Limongi, S. C. O., & Andrade, C. R. F. de. (2013). Oral Motor Movements and Swallowing in Patients with Myotonic Dystrophy Type 1. Dysphagia, 28( 3), 446-454. doi:10.1007/s00455-013-9458-9
    • NLM

      Ercolin B, Sassi FC, Mangilli LD, Mendonça LIZ, Limongi SCO, Andrade CRF de. Oral Motor Movements and Swallowing in Patients with Myotonic Dystrophy Type 1 [Internet]. Dysphagia. 2013 ; 28( 3): 446-454.Available from: http://link.springer.com/article/10.1007/s00455-013-9458-9
    • Vancouver

      Ercolin B, Sassi FC, Mangilli LD, Mendonça LIZ, Limongi SCO, Andrade CRF de. Oral Motor Movements and Swallowing in Patients with Myotonic Dystrophy Type 1 [Internet]. Dysphagia. 2013 ; 28( 3): 446-454.Available from: http://link.springer.com/article/10.1007/s00455-013-9458-9

    Referências citadas na obra
    Harley HC, Brook JD, Rundle SA, et al. Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy. Nature. 1992;355(6360):545–6.
    Shaw DJ, Harper PS. Myotonic dystrophy: developments in molecular genetics. Br Med Bull. 1989;45(3):745–59.
    Harley HG, Rundle SA, MacMillan JC, et al. Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy. Am J Hum Genet. 1993;52(6):1164–74.
    Mathieu J, Allard P, Potvin L, et al. A 10 year study of mortality in a cohort of patients with myotonic dystrophy. Neurology. 1999;52(8):1658–62.
    Yotova V, Labuda D, Zietkiewicz E, et al. Anatomy of a founder effect: myotonic dystrophy in Northeastern Quebec. Hum Genet. 2005;117(2–3):177–87.
    Gagnon C, Chouinard MC, Laberge L, et al. Health supervision and anticipatory guidance in adult myotonic dystrophy type 1. Neuromuscul Disord. 2010;20(12):847–51. doi: 10.1016/j.nmd.2010.08.006 .
    Peñarrocha M, Bagán JV, Vilchez J, et al. Oral alterations in Steinert’s myotonic dystrophy: a presentation of two cases. Oral Surg Oral Med Oral Pathol. 1990;69(6):698–700.
    Mercier J, Bennani F, Ferri J, et al. Maxillofacial manifestations of Steinert’s myotonic dystrophy. Rev Stomatol Chir Maxillofac. 1995;96(2):74–82.
    Sovari AA, Bodine CK, Farokin F. Cardiovascular manifestation of myotonic dystrophy-1. Cardiol Rev. 2007;15(4):191–4. doi: 10.1097/CRD.0b013e318070d1a7 .
    Ramig LA, Scherer RC, Titze IR, et al. Acoustic analysis of voice of patients with neurologic disease: rationale and preliminary data. Ann Otol Rhinol Laryngol. 1988;97(2 Pt 1):164–72.
    Salomonson J, Kawamoto H, Wilson J. Velopharyngeal incompetence as the presenting symptom of myotonic dystrophy. Cleft Palate J. 1988;25(3):296–300.
    Weinberg B, Bosma JF, Shanks JC, et al. Myotonic dystrophy initially manifested by speech disability. J Speech Hear Disord. 1968;33(1):51–9.
    de Swart BJ, van Engelen BG, van de Kerkhof JP, et al. Myotonia and flaccid dysarthria in patients with adult onset myotonic dystrophy. J Neurol Neurosurg Psychiatry. 2004;75(10):1480–2. doi: 10.1136/jnnp.2003.032151 .
    Darley FL, Aronson AE, Brown JR. Motor speech disorders. Philadelphia: WB Saunders; 1975.
    McNeil MR. Clinical management of sensorimotor speech disorders. Stuttgart: Thieme; 1997.
    de Die Smulders CE, Höweler CJ, Thijs C et al. Age and causes of death in adult-onset myotonic dystrophy. Brain. 1998;121:1557-63.
    Mizuno T, Komaki H, Sasaki M, et al. Efficacy and tolerance of gastrostomy feeding in Japanese muscular dystrophy patients. Brain Dev. 2012;34:756–62. doi: 10.1016/j.braindev.2011.11.012 .
    Peric S, Rakocevic-Stojanovic V, Basta I, et al. Influence of multisystemic affection on health-related quality of life in patients with myotonic dystrophy type 1. Clin Neurol Neurosurg. 2013;115(3):270–5. doi: 10.1016/j.clineuro.2012.05.015 .
    Bellini M, Biagi S, Stasi C, et al. Gastrointestinal manifestations in myotonic muscular dystrophy. World J Gastroenterol. 2006;12:1821–8.
    Harvey JC, Sherbourne DH, Siegel CI. Smooth muscle involvement in myotonic dystrophy. Am J Med. 1965;39:81–90.
    Ertekin C, Yüceyar N, Aydogdu I, et al. Electrophysiological evaluation of oropharyngeal swallowing in myotonic dystrophy. J Neurol Neurosurg Psychiatry. 2001;70(3):363–71. doi: 10.1136/jnnp.70.3.363 .
    Chiappetta AL, Oda AL, Zanoteli E et al. Oropharyngeal dysphagia in the myotonic dystrophy: phonoaudiological evaluation and nasofibrolaryngoscopical analysis. Arq Neuropsiquiatr. 2001;59(2-B):394–400.
    Turner C, Hilton-Jones D. The myotonic dystrophies: diagnosis and management. J Neurol Neurosurg Psychiatry. 2010;81(4):358–67. doi: 10.1136/jnnp.2008.158261 .
    Eisenhuber E, Schima W, Schober E, et al. Videofluoroscopic assessment of patients with dysphagia: pharyngeal retention is a predictive factor for aspiration. AJR Am J Roentgenol. 2002;178(2):393–8.
    Ertekin C, Aydogdu I, Yüceyar N. Piecemeal deglutition and dysphagia limit in normal subjects and in patients with swallowing disorders. J Neurol Neurosurg Psychiatry. 1996;61(5):491–6.
    Vaiman M. Standardization of surface electromyography utilized to evaluate patients with dysphagia. Head Face Med. 2007;3:26. doi: 10.1186/1746-160X-3-26 .
    Ertekin C, Aydogdu I, Yüceyar N, et al. Electrodiagnostic methods for neurogenic dysphagia. Electroencephalogr Clin Neurophysiol. 1988;109(4):331–40.
    Alfonsi E, Veríssimo M, Merlo IM, et al. Electrophysiologic patterns of oral-pharyngeal swallowing in parkinsonian syndromes. Neurology. 2007;68(8):583–90.
    Coriolano MD, Belo LR, Carneiro D, et al. Swallowing in patients with Parkinson’s disease: a surface electromyography study. Dysphagia. 2012;27(4):550–5. doi: 10.1007/s00455.012-9406-0 .
    American Speech-Language-Hearing Association. National Outcome Measurement System (NOMS). Adult Speech-Language Pathology training manual. Rockville, MD: ASHA; 1998.
    Wesling M, Brady S, Jensen M, et al. Dysphagia outcomes in patients with brain tumors undergoing inpatient rehabilitation. Dysphagia. 2003;18:203–10. doi: 10.1007/s00455-002-0098-8 .
    Felício CM, Ferreira CL. Protocol of orofacial myofunctional evaluation with scores. Int J Pediatr Otorhinolaryngol. 2008;72(3):367–75. doi: 10.1016/j.ijporl.2007.11.012 .
    Felício CM, Medeiros APM, Melchior MO. Validity of the ‘protocol of oro-facial myofunctional evaluation with scores’ for young and adult subjects. J Oral Rehabil. 2012;39:744–53. doi: 10.11/j.l365-2842.2012.02336.x .
    Contardi S, Pizza F, Falzoni F, et al. Development of a disability scale for myotonic dystrophy type 1. Acta Neurol Scand. 2012;125:431–8. doi: 10.1111/j.1600-0404.2011.01587.x .
    Hammarén E, Kjellby-Wendt G, Linderberg C. Quantification of mobility impairment and self-assessment of stiffness in patients with myotonia congenita by the physiotherapist. Neuromuscul Disord. 2005;15(9–10):610–7. doi: 10.1016/j.nmd.2005.07.002 .
    Kierkegaard M, Tollbäck A. Reliability and feasibility of the six minute walk test in subjects with myotonic dystrophy. Neuromuscul Disord. 2007;17(11–12):943–9. doi: 10.1016/j.nmd.2007.08.003 .
    Moxley RT 3rd, Logigian EL, Martens WB, et al. Computerized hand grip myometry reliably measures myotonia and muscle strength in myotonic dystrophy (DM1). Muscle Nerve. 2007;36(3):320–8. doi: 10.1002/mus.20822 .
    Sansone V, Marinou K, Salvucci J, et al. Quantitative myotonia assessment: an experimental protocol. Neurol Sci. 2000;21(5 Suppl):S971–4.
    Vincent KA, Carr AJ, Walburn J, et al. Construction and validation of a quality of life questionnaire for neuromuscular disease (INQoL). Neurology. 2007;68(13):1051–7.
    Felício CM, Folha GA, Ferreira CLP, Medeiros APM. Expanded protocol of orofacial myofunctional evaluation with scores: validity and reliability. Int J Pediatr Otorhinolaryngol. 2010;74:1230–9. doi: 10.1016/j.ijporl.2010.07.021 .
    Vaiman M, Eviatar E, Segal S. Evaluation of normal deglutition with the help of rectified surface electromyography records. Dysphagia. 2004;19:125–32. doi: 10.1007/s00455-003-0504-x .
    Ertekin C, Tarlaci S, Aydoglu I, et al. Electrophysiological evaluation of pharyngeal phase of swallowing in patients with Parkinson’s disease. Mov Disord. 2002;17(5):942–9. doi: 10.1002/mds.10240 .
    Conravey A, Santana-Gould L. Myotonia congenita and myotonic dystrophy: surveillance and management. Curr Treat Options Neurol. 2010;12(1):16–28. doi: 10.1007/s11940-009-0055-z .
    Araújo FS, Bessa Júnior RC, Castro CH, et al. Anesthesia in a patient with Steinert disease: case report. Rev Bras Anestesiol. 2006;56(6):649–53.
    Buchholz DW. Dysphagia associated with neurological disorders. Acta Otorhinolaryngol Belg. 1994;48(2):143–55.
    Fu YH, Pizzuti A, Fenwick RG Jr, et al. An unstable triplet repeat in a gene related to myotonic muscular dystrophy. Science. 1992;255(5049):1256–8.
    Ambrosio AR, Trevilatto PC, Martins LP, et al. Electromyographic evaluation of the upper lip according to the breathing mode: a longitudinal study. Braz Oral Res. 2009;23(4):415–23.
    Wilbourn AJ, Ferrante MA. Clinical electromyography. In: Joynt RJ, Griggs RC editors. Baker’s clinical neurology. Philadelphia: WB Saunders; 2000 (book on CD-ROM).
    Cooper RG, Stokes MJ, Edwards RH. Physiological characterization of the “warm-up” effect of activity in patients with myotonic dystrophy. J Neurol Neurosurg Psychiatry. 1988;51(9):1134–41.