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                             13 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A c.1775C > T Point Mutation of Sodium Channel Alfa Subunit Gene (SCN4A) in a Three-Generation Sardinian Family with Sodium Channel Myotonia Campanale, Carmen

11 3 p. 725-734
artikel
2 Detection of Autoantibodies Against the Acetylcholine Receptor, Evaluation of Commercially Available Methodologies: Fixed Cell-Based Assay, Radioimmunoprecipitation Assay and Enzyme-Linked Immunosorbent Assay1 Diogenes, Larissa

11 3 p. 613-623
artikel
3 Disease Trajectories in the Revised Hammersmith Scale in a Cohort of Untreated Patients with Spinal Muscular Atrophy types 2 and 3 Wolfe, Amy

11 3 p. 665-677
artikel
4 Improving Diagnostic Precision: Phenotype-Driven Analysis Uncovers a Maternal Mosaicism in an Individual with RYR1-Congenital Myopathy Estévez-Arias, Berta

11 3 p. 647-653
artikel
5 Increase in Full-Length Dystrophin by Exon Skipping in Duchenne Muscular Dystrophy Patients with Single Exon Duplications: An Open-label Study Nicolau, Stefan

11 3 p. 679-685
artikel
6 Management of Select Adverse Events Following Delandistrogene Moxeparvovec Gene Therapy for Patients With Duchenne Muscular Dystrophy Zaidman, Craig M.

11 3 p. 687-699
artikel
7 Natural History of Mandibular Function in Spinal Muscular Atrophy Types 2 and 3 van Bruggen, H. Willemijn

11 3 p. 655-664
artikel
8 Novel Genetic and Biochemical Insights into the Spectrum of NEFL-Associated Phenotypes Della Marina, Adela

11 3 p. 625-645
artikel
9 Patient-Reported Outcome Measures in Neuromuscular Diseases: A Scoping Review Voet, Nicoline

11 3 p. 567-577
artikel
10 Predictors of Loss of Ambulation in Duchenne Muscular Dystrophy: A Systematic Review and Meta-Analysis Landfeldt, E.

11 3 p. 579-612
artikel
11 Stride Velocity 95th Centile Detects Decline in Ambulatory Function Over Shorter Intervals than the 6-Minute Walk Test or North Star Ambulatory Assessment in Duchenne Muscular Dystrophy Rabbia, Michael

11 3 p. 701-714
artikel
12 The Association Between Physical Activity/Heart Rate Variability Data Obtained Using a Wearable Device and Timed Motor Functional Tests in Patients with Duchenne Muscular Dystrophy: A Pilot Study Nakamura, Akinori

11 3 p. 715-724
artikel
13 Treatment Approaches for Altered Facial Expression: A Systematic Review in Facioscapulohumeral Muscular Dystrophy and Other Neurological Diseases Rasing, Nathaniël B.

11 3 p. 535-565
artikel
                             13 gevonden resultaten
 
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