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                             19 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A novel MFN2 mutation causes variable clinical severity in a multi-generational CMT2 family Dankwa, Lois
2019
29 2 p. 134-137
artikel
2 Autologous hematopoietic stem cell transplantation in a patient with refractory seropositive myasthenia gravis: A case report Sossa Melo, Claudia Lucía
2019
29 2 p. 142-145
artikel
3 Clinical spectrum of neuromuscular complications after immune checkpoint inhibition Puwanant, Araya
2019
29 2 p. 127-133
artikel
4 Colonic distension treatment in Duchenne muscular dystrophy Fiorentino, Giuseppe
2019
29 2 p. 157-158
artikel
5 Colonic distension treatment in Duchenne muscular dystrophy - response Vianello, Andrea
2019
29 2 p. 159
artikel
6 Dominantly inherited distal nemaline/cap myopathy caused by a large deletion in the nebulin gene Kiiski, Kirsi J.
2019
29 2 p. 97-107
artikel
7 Dropped head syndrome as a manifestation of Charcot–Marie–Tooth disease type 4C de Oliveira, Camila Maria
2019
29 2 p. 138-141
artikel
8 Editorial Board 2019
29 2 p. IFC
artikel
9 Long-term follow-up and characteristic pathological findings in severe nemaline myopathy due to LMOD3 mutations Michael, Eva
2019
29 2 p. 108-113
artikel
10 Muscle hypertrophy in amyloid myopathy Tasca, Giorgio
2019
29 2 p. 150-151
artikel
11 Neuromuscular disorders in Anatolia – A personal review Topaloğlu, Haluk
2019
29 2 p. 152-156
artikel
12 [No title] Damian, Heidelinde
2019
29 2 p. 164
artikel
13 [No title] McEntagart, Meriel
2019
29 2 p. 163
artikel
14 Professor Frank Lehmann-Horn, M.D. (1948–2018) Rüdel, Reinhardt
2019
29 2 p. 165-166
artikel
15 Replication studies of MIR149 association in Charcot–Marie–Tooth disease type 1A in a European population Tao, Feifei
2019
29 2 p. 160-162
artikel
16 Replication studies of MIR149 association in Charcot–Marie–Tooth disease type 1A in a European population - response Choi, Byung-Ok
2019
29 2 p. 160-162
artikel
17 Spinal muscular atrophy with respiratory distress type 1: A multicenter retrospective study Viguier, Agnès
2019
29 2 p. 114-126
artikel
18 Targeted gene approach with biochemical assay confirms ABCD1 mutation of X-linked adrenoleukodystrophy in a 62-year-old man with gait imbalance Mauermann, Michelle L.
2019
29 2 p. 146-149
artikel
19 The clinical management of neuromuscular disorders in intensive care Damian, Maxwell S.
2019
29 2 p. 85-96
artikel
                             19 gevonden resultaten
 
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