| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A New Point Mutation in the PMP22 Gene in a Family Suffering From Atypical HNPP
|
Benquey, T.
|
|
|
7 |
4 |
p. 505-510
|
artikel
|
| 2 |
Correlation Between Quantitative MRI and Muscle Histopathology in Muscle Biopsies from Healthy Controls and Patients with IBM, FSHD and OPMD
|
Lassche, Saskia
|
|
|
7 |
4 |
p. 495-504
|
artikel
|
| 3 |
Decision-Making And Selection Bias in Four Observational Studies on Duchenne and Becker Muscular Dystrophy
|
Naarding, Karin J.
|
|
|
7 |
4 |
p. 433-442
|
artikel
|
| 4 |
Facilitators and Barriers to Wearing Hand Orthoses by Adults with Duchenne Muscular Dystrophy: A Mixed Methods Study Design
|
Houwen-van Opstal, S.L.S.
|
|
|
7 |
4 |
p. 467-475
|
artikel
|
| 5 |
Familial Oculo-Leptomeningeal Transthyretin Amyloidosis Caused by Leu55Arg Mutation
|
Kleefeld, Felix
|
|
|
7 |
4 |
p. 515-519
|
artikel
|
| 6 |
Ganglionopathies Associated with MERRF Syndrome: An Original Report
|
Michaud, Maud
|
|
|
7 |
4 |
p. 419-423
|
artikel
|
| 7 |
Identification and Characterization of Splicing Defects by Single-Molecule Real-Time Sequencing Technology (PacBio)
|
Savarese, Marco
|
|
|
7 |
4 |
p. 477-481
|
artikel
|
| 8 |
Induction of Skeletal Muscle Progenitors and Stem Cells from human induced Pluripotent Stem Cells
|
Sato, Takahiko
|
|
|
7 |
4 |
p. 395-405
|
artikel
|
| 9 |
Lower Extremity Muscle Involvement in the Intermediate and Bethlem Myopathy Forms of COL6-Related Dystrophy and Duchenne Muscular Dystrophy: A Cross-Sectional Study
|
Batra, Abhinandan
|
|
|
7 |
4 |
p. 407-417
|
artikel
|
| 10 |
Measuring Outcomes in Adults with Spinal Muscular Atrophy – Challenges and Future Directions – Meeting Report
|
Sansone, V.A.
|
|
|
7 |
4 |
p. 523-534
|
artikel
|
| 11 |
Natural History of Type 1 Spinal Muscular Atrophy in a Series of Argentinian Children
|
Aguerre, V.
|
|
|
7 |
4 |
p. 453-458
|
artikel
|
| 12 |
Neuroanatomical Models of Muscle Strength and Relationship to Ambulatory Function in Spinal Muscular Atrophy
|
Rodriguez-Torres, Rafael
|
|
|
7 |
4 |
p. 459-466
|
artikel
|
| 13 |
Phenotypic Spectrum of Myopathies with Recessive Anoctamin-5 Mutations
|
Vázquez, José
|
|
|
7 |
4 |
p. 443-451
|
artikel
|
| 14 |
Respiratory Dysfunction in Becker Muscular Dystrophy Patients: A Case Series and Autopsy Report
|
Mori-Yoshimura, Madoka
|
|
|
7 |
4 |
p. 425-431
|
artikel
|
| 15 |
Severe inflammatory myopathy in a pulmonary carcinoma patient treated with Pembrolizumab: An alert for myologists
|
Peverelli, L.
|
|
|
7 |
4 |
p. 511-514
|
artikel
|
| 16 |
Swallowing, Chewing and Speaking: Frequently Impaired in Oculopharyngeal Muscular Dystrophy
|
Kroon, Rosemarie H.M.J.M.
|
|
|
7 |
4 |
p. 483-494
|
artikel
|
| 17 |
Taking a Strohl Through History: Putting Strohl Back in Guillain-Barré-Strohl Syndrome
|
Bondi, Steven
|
|
|
7 |
4 |
p. 521-522
|
artikel
|
| 18 |
Towards Central Nervous System Involvement in Adults with Hereditary Myopathies
|
Reimann, Jens
|
|
|
7 |
4 |
p. 367-393
|
artikel
|
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