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Amyotrophic Lateral Sclerosis Volume 12, 2011 - Issue 5
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Research Article

Vocal cord paralysis and rapid progressive motor neuron disease by the I113F mutation in SOD1 gene

Andreas HermannDepartment of Neurology, Dresden University of Technology;Centre for Regenerative Therapies Dresden (CRTD), Dresden University of TechnologyCorrespondence[email protected]
,
Ulrike ReunerDepartment of Neurology, Dresden University of Technology
,
Georg Ziethe St.-Marien-Hospital, Dresden
,
Andreas Bräuer St.-Marien-Hospital, Dresden
,
Uta Gölnitz Centogene, Insitute of Molecular Diagnostic, Rostock
,
Arndt Rolfs Centogene, Insitute of Molecular Diagnostic, Rostock; Albrecht-Kossel-Institute for Neuroregeneration, University Rostock, Rostock, Germany
&
Claudia RicciDepartment of Neuroscience, University of Siena, Siena, Italy
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Pages 382-384 | Received 05 Oct 2010, Accepted 18 Feb 2011, Published online: 17 Mar 2011

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Paola Origone, Claudia Caponnetto, Vittorio Mantero, Elena Cichero, Paola Fossa, Alessandro Geroldi, Simonetta Verdiani, Emilia Bellone, Gianluigi Mancardi & Paola Mandich. (2012) Fast course ALS presenting with vocal cord paralysis: Clinical features, bioinformatic and modelling analysis of the novel SOD1 Gly147Ser mutation. Amyotrophic Lateral Sclerosis 13:1, pages 144-148.
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Articles from other publishers (5)

Saiumaeswar Yogakanthi, Christine Wools & Susan Mathers. (2021) Unilateral vocal cord adductor weakness: an atypical manifestation of motor neurone disease. BMJ Neurology Open 3:2, pages e000205.
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Giuliana Capece, Mauro Ceroni, Enrico Alfonsi, Ilaria Palmieri, Cristina Cereda & Luca Diamanti. (2021) Case Report: Laryngospasm as Initial Manifestation of Amyotrophic Lateral Sclerosis in a Long-Survival Patient With Heterozygous p.D90A – SOD1 Mutation. Frontiers in Neurology 12.
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Brian Gordon, Eimear Joyce & Timothy J Counihan. (2021) Stridor: a rare presentation of motor neuron disease. BMJ Case Reports 14:7, pages e241923.
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Rebecca Shaw, Cristina Dias, Jeffrey Ludemann, Rosemarie Rupps, Vance Tsai & Anna Lehman. (2018) Familial impairment of vocal cord mobility in childhood with clubfoot. Clinical Dysmorphology 27:4, pages 116-121.
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Amy K Hsu, David E. Rosow, Robert J. Wallerstein & Max M. April. (2015) Familial congenital bilateral vocal fold paralysis: A novel gene translocation. International Journal of Pediatric Otorhinolaryngology 79:3, pages 323-327.
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