| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Ataxia-oculomotor apraxia 2 patients show no increased sensitivity to ionizing radiation
|
Nahas, S.A.
|
|
2007
|
|
11-12 |
p. 968-969
2 p.
|
artikel
|
| 2 |
Behavior patterns in Duchenne muscular dystrophy: Report on the Parent Project Muscular Dystrophy behavior workshop 8–9 of December 2006, Philadelphia, USA
|
Poysky, James
|
|
2007
|
|
11-12 |
p. 986-994
9 p.
|
artikel
|
| 3 |
Ciliary neurotrophic factor null alleles are not a risk factor for Charcot-Marie-Tooth disease, hereditary neuropathy with pressure palsies and amyotrophic lateral sclerosis
|
Van Vught, Paul W.J.
|
|
2007
|
|
11-12 |
p. 964-967
4 p.
|
artikel
|
| 4 |
(Contents continued from back cover)
|
|
|
2007
|
|
11-12 |
p. III-
1 p.
|
artikel
|
| 5 |
CRISPR-mediated correction of skeletal muscle Ca2+ handling in a novel DMD patient-derived pluripotent stem cell model
|
Morera, Cristina
|
|
|
|
11-12 |
p. 908-922
|
artikel
|
| 6 |
Diagnostic yield of a practical electrodiagnostic protocol discriminating between different congenital myasthenic syndromes
|
Stojkovic, Tanya
|
|
|
|
11-12 |
p. 870-878
|
artikel
|
| 7 |
Dubowitz Neuromuscular Centre on the move
|
|
|
2007
|
|
11-12 |
p. 995-
1 p.
|
artikel
|
| 8 |
Dysferlinopathy in the Jews of the Caucasus: A frequent mutation in the dysferlin gene
|
Leshinsky-Silver, E.
|
|
2007
|
|
11-12 |
p. 950-954
5 p.
|
artikel
|
| 9 |
Dystrophin levels as low as 30% are sufficient to avoid muscular dystrophy in the human
|
Neri, Marcella
|
|
2007
|
|
11-12 |
p. 913-918
6 p.
|
artikel
|
| 10 |
Dystrophinopathy and the brain: A parent project muscular dystrophy (PPMD) meeting report November 11-12, 2021, New York City, NY
|
Colvin, Mary K.
|
|
|
|
11-12 |
p. 935-944
|
artikel
|
| 11 |
Editorial Board
|
|
|
|
|
11-12 |
p. IFC
|
artikel
|
| 12 |
Editorial Board
|
|
|
2007
|
|
11-12 |
p. IFC-
1 p.
|
artikel
|
| 13 |
False negative histochemical reaction for myophosphorylase activity in fulminant sepsis due to methicillin resistant Staphylococcus aureus
|
Cristina Pacheco, M.
|
|
2007
|
|
11-12 |
p. 983-985
3 p.
|
artikel
|
| 14 |
Highly asymmetrical distribution of muscle wasting correlates to the heteroplasmy in a patient carrying a large-scale mitochondrial DNA deletion: a novel pathophysiological mechanism for explaining asymmetry in mitochondrial myopathies
|
Masingue, M.
|
|
|
|
11-12 |
p. 923-930
|
artikel
|
| 15 |
Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiency
|
Musumeci, Olimpia
|
|
2007
|
|
11-12 |
p. 960-963
4 p.
|
artikel
|
| 16 |
Intermediate filament-like protein syncoilin in normal and myopathic striated muscle
|
McCullagh, Karl J.A.
|
|
2007
|
|
11-12 |
p. 970-979
10 p.
|
artikel
|
| 17 |
John Newsom-Davis 1932–2007
|
Engel, Andrew G.
|
|
2007
|
|
11-12 |
p. 997-998
2 p.
|
artikel
|
| 18 |
Long term follow-up of scoliosis progression in type II SMA patients
|
Coratti, Giorgia
|
|
|
|
11-12 |
p. 879-885
|
artikel
|
| 19 |
Long term noninvasive ventilation and continuous positive airway pressure in children with neuromuscular diseases in France
|
Allaer, Laura
|
|
|
|
11-12 |
p. 886-892
|
artikel
|
| 20 |
Low bone mineral density and decreased bone turnover in Duchenne muscular dystrophy
|
Söderpalm, Ann-Charlott
|
|
2007
|
|
11-12 |
p. 919-928
10 p.
|
artikel
|
| 21 |
Masseter muscle volume as a disease marker in adult-onset myotonic dystrophy type 1
|
Oliwa, Agata
|
|
|
|
11-12 |
p. 893-902
|
artikel
|
| 22 |
Muscle lymphocytic infiltrates in thymoma-associated myasthenia gravis are phenotypically different from those in polymyositis
|
Zamecnik, Josef
|
|
2007
|
|
11-12 |
p. 935-942
8 p.
|
artikel
|
| 23 |
Muscle ultrasound in hereditary muscle disease
|
Hannaford, Andrew
|
|
|
|
11-12 |
p. 851-863
|
artikel
|
| 24 |
Myasthenia gravis in South Africans: Racial differences in clinical manifestations
|
Heckmann, J.M.
|
|
2007
|
|
11-12 |
p. 929-934
6 p.
|
artikel
|
| 25 |
Novel association of gluten sensitivity with immune-mediated neuromuscular syndrome in a dog
|
Kolb, Ninja
|
|
|
|
11-12 |
p. 903-907
|
artikel
|
| 26 |
OBC: contents
|
|
|
2007
|
|
11-12 |
p. OBC-
1 p.
|
artikel
|
| 27 |
POEMS syndrome: relapse after successful autologous peripheral blood stem cell transplantation
|
Giglia, F.
|
|
2007
|
|
11-12 |
p. 980-982
3 p.
|
artikel
|
| 28 |
Reliability and feasibility of the six minute walk test in subjects with myotonic dystrophy
|
Kierkegaard, Marie
|
|
2007
|
|
11-12 |
p. 943-949
7 p.
|
artikel
|
| 29 |
Report on the 6th Annual Scientific Meeting of the Asian and Oceanian Myology Center, Penang 2007
|
|
|
2007
|
|
11-12 |
p. 995-996
2 p.
|
artikel
|
| 30 |
Risk of malignant hyperthermia in patients carrying a variant in the skeletal muscle ryanodine receptor 1 gene
|
Janssens, Lise
|
|
|
|
11-12 |
p. 864-869
|
artikel
|
| 31 |
Subtle central and peripheral nervous system abnormalities in a family with centronuclear myopathy and a novel dynamin 2 gene mutation
|
Echaniz-Laguna, Andoni
|
|
2007
|
|
11-12 |
p. 955-959
5 p.
|
artikel
|
| 32 |
13th International WMS Congress
|
|
|
2007
|
|
11-12 |
p. II-
1 p.
|
artikel
|
| 33 |
Two tales of LPIN1 deficiency: from fatal rhabdomyolysis to favorable outcome of acute compartment syndrome
|
Kahraman, Ayca Burcu
|
|
|
|
11-12 |
p. 931-934
|
artikel
|
| 34 |
WMS application form
|
|
|
2007
|
|
11-12 |
p. I-
1 p.
|
artikel
|
| 35 |
WMS 2023 Congress announcement
|
|
|
|
|
11-12 |
p. III
|
artikel
|
| 36 |
WMS 2023 Flyer
|
|
|
|
|
11-12 |
p. II
|
artikel
|
| 37 |
WMS Information
|
|
|
|
|
11-12 |
p. I
|
artikel
|
Tijdschrift beschrijving