Diagnosis and management of spinal muscular atrophy: Part 2: Pulmonary and acute care; medications, supplements and immunizations; other organ systems; and ethics (Unknown)
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In:
NEUROMUSCULAR DISORDERS
;
28
, 3
;
197-207
;
2018
-
ISSN:
- Article (Journal) / Print
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Title:Diagnosis and management of spinal muscular atrophy: Part 2: Pulmonary and acute care; medications, supplements and immunizations; other organ systems; and ethics
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Contributors:Finkel, Richard S. ( author ) / Mercuri, Eugenio ( author ) / Meyer, Oscar H. ( author ) / Simonds, Anita K. ( author ) / Schroth, Mary K. ( author ) / Graham, Robert J. ( author ) / Kirschner, Janbernd ( author ) / Iannaccone, Susan T. ( author ) / Crawford, Thomas O. ( author ) / Woods, Simon ( author )
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Published in:NEUROMUSCULAR DISORDERS ; 28, 3 ; 197-207
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Publisher:
- New search for: Elsevier Science B.V., Amsterdam.
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Publication date:2018-01-01
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Size:11 pages
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ISSN:
-
Type of media:Article (Journal)
-
Type of material:Print
-
Language:Unknown
- New search for: 616.83
- Further information on Dewey Decimal Classification
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Classification:
DDC: 616.83 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 28, Issue 3
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 197
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Diagnosis and management of spinal muscular atrophy: Part 2: Pulmonary and acute care; medications, supplements and immunizations; other organ systems; and ethicsFinkel, Richard S. / Mercuri, Eugenio / Meyer, Oscar H. / Simonds, Anita K. / Schroth, Mary K. / Graham, Robert J. / Kirschner, Janbernd / Iannaccone, Susan T. / Crawford, Thomas O. / Woods, Simon et al. | 2018
- 208
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Correlation between SMA type and SMN2 copy number revisited: An analysis of 625 unrelated Spanish patients and a compilation of 2834 reported casesCalucho, Maite / Bernal, Sara / Alías, Laura / March, Francesca / Venceslá, Adoración / Rodríguez-Álvarez, Francisco J. / Aller, Elena / Fernández, Raquel M. / Borrego, Salud / Millán, José M. et al. | 2018
- 216
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Childhood-onset form of myotonic dystrophy type 1 and autism spectrum disorder: Is there comorbidity?Angeard, N. / Huerta, E. / Jacquette, A. / Cohen, D. / Xavier, J. / Gargiulo, M. / Servais, L. / Eymard, B. / Héron, D. et al. | 2018
- 222
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Genotype and other determinants of respiratory function in myotonic dystrophy type 1Boussaïd, Ghilas / Wahbi, Karim / Laforet, Pascal / Eymard, Bruno / Stojkovic, Tanya / Behin, Anthony / Djillali, Annane / Orlikowski, David / Prigent, Hélène / Lofaso, Frédéric et al. | 2018
- 229
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Falls and resulting fractures in Myotonic Dystrophy: Results from a multinational retrospective surveyJiménez-Moreno, A.C. / Raaphorst, J. / Babačić, H. / Wood, L. / van Engelen, B. / Lochmüller, H. / Schoser, B. / Wenninger, S. et al. | 2018
- 236
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A boy with neck weaknessYiş, Uluç / Becker, Kerstin / Çırak, Sebahattin et al. | 2018
- 238
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Specific muscle strength is reduced in facioscapulohumeral dystrophy: An MRI based musculoskeletal analysisMarra, Marco A. / Heskamp, Linda / Mul, Karlien / Lassche, Saskia / van Engelen, Baziel G.M. / Heerschap, Arend / Verdonschot, Nico et al. | 2018
- 246
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Imaging of respiratory muscles in neuromuscular disease: A reviewHarlaar, L. / Ciet, P. / van der Ploeg, A.T. / Brusse, E. / van der Beek, N.A.M.E. / Wielopolski, P.A. / de Bruijne, M. / Tiddens, H.A.W.M. / van Doorn, P.A. et al. | 2018
- 257
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Prevalence of adult Pompe disease in patients with proximal myopathic syndrome and undiagnosed muscle biopsyGolsari, Amir / Nasimzadah, Arzoo / Thomalla, Götz / Keller, Sarah / Gerloff, Christian / Magnus, Tim et al. | 2018
- 262
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A database for screening and registering late onset Pompe disease in TurkeyGokyigit, Munevver Celik / Ekmekci, Hakan / Durmus, Hacer / Karlı, Necdet / Koseoglu, Emel / Aysal, Fikret / Kotan, Dilcan / Ali, Asuman / Koytak, Pınar Kahraman / Karasoy, Hatice et al. | 2018
- 268
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Hereditary myopathy with early respiratory failure (HMERF): Still rare, but common enoughTasca, Giorgio / Udd, Bjarne et al. | 2018
- 277
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Ophthalmoplegia due to concurrent thyrotoxicosis and myasthenia gravisRay, Sucharita / Vibha, Deepti / Gupta, Gauri / Prasad, Kameshwar / Srivastava, Achal K. / Shukla, Garima et al. | 2018
- 278
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DOK7 myasthenic syndrome with subacute adult onset during pregnancy and partial response to fluoxetineSantos, Mariana / Cruz, Simão / Peres, João / Santos, Luís / Tavares, Purificação / Basto, Jorge Pinto / Salgado, Vasco / Valverde, Ana Herrero et al. | 2018
- 283
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Mitophagy in three cases of immune-mediated necrotizing myopathy associated with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase autoantibodies: ultrastructural and immunohistochemical studiesMatsubara, Shiro / Bokuda, Kota / Asano, Yuri / Morishima, Ryo / Sugaya, Keizo / Miyamoto, Kazuhito / Koide, Reiji / Komori, Takashi / Suzuki, Shigeaki / Nishino, Ichizo et al. | 2018
- 289
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228th ENMC International Workshop:Toussaint, Michel / Chatwin, Michelle / Gonzales, Jesus / Berlowitz, David J. et al. | 2018
- 299
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Book reviewTedesco, Francesco Saverio et al. | 2018
- 300
-
Giovanni Nigro 1931–2017Politano, Luisa / Nigro, Vincenzo et al. | 2018
-
Editorial Board| 2018
-
Update in NMD Announcement| 2018