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                             16 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A new severe mutation in the SLC5A7 gene related to congenital myasthenic syndrome type 20 Pardal-Fernández, J.M.
2018
28 10 p. 881-884
artikel
2 A novel MYH7 founder mutation causing Laing distal myopathy in Southern Spain Carbonell-Corvillo, P.
2018
28 10 p. 828-836
artikel
3 Characteristic findings of skeletal muscle MRI in caveolinopathies Ishiguro, Kumiko
2018
28 10 p. 857-862
artikel
4 Corrigendum to “Congenital myasthenic syndromes in Turkey: Clinical clues and prognosis with long term follow-up” [Neuromuscular Disorders 28/4 (2018) 315–322] Durmus, Hacer
2018
28 10 p. 896
artikel
5 Does albuterol have an effect on neuromuscular junction dysfunction in spinal muscular atrophy? Pera, Maria Carmela
2018
28 10 p. 863-864
artikel
6 Editorial Board 2018
28 10 p. IFC
artikel
7 Graves’ disease and celiac disease in a patient with myotonic dystrophy type 2 Damen, M.J.
2018
28 10 p. 878-880
artikel
8 GsMTx4-D provides protection to the D2.mdx mouse Ward, Christopher W.
2018
28 10 p. 868-877
artikel
9 Lower-extremity magnetic resonance imaging in patients with hyperkalemic periodic paralysis carrying the SCN4A mutation T704M: 30-month follow-up of seven patients Jeong, Ha-Neul
2018
28 10 p. 837-845
artikel
10 Myoglobinuria in two patients with Duchenne muscular dystrophy after treatment with zoledronate: a case-report and call for caution Ivanyuk, Anton
2018
28 10 p. 865-867
artikel
11 National registry of patients with Fukuyama congenital muscular dystrophy in Japan Ishigaki, Keiko
2018
28 10 p. 885-893
artikel
12 New variant of necklace fibres display peculiar lysosomal structures and mitophagy Rinnenthal, Jan Leo
2018
28 10 p. 846-856
artikel
13 Non invasive mechanical ventilation in DM1: The strong correlation between lung function, neurological-cognitive function and CTG repeats Lofaso, Frédéric
2018
28 10 p. 894-895
artikel
14 Non invasive mechanical ventilation in DM1: The strong correlation between lung function, neurological-cognitive function and CTG repeats Fiorentino, Giuseppe
2018
28 10 p. 894-895
artikel
15 Personalized gene and cell therapy for Duchenne Muscular Dystrophy Barthélémy, Florian
2018
28 10 p. 803-824
artikel
16 Self-diagnosis of a triple trouble Schoser, B.
2018
28 10 p. 825-827
artikel
                             16 gevonden resultaten
 
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