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                             19 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A new pseudoexon activation due to ultrarare branch point formation in Duchenne muscular dystrophy Xie, Zhiying

35 C p. 8-12
artikel
2 Corrigendum to “NMNAT1 and hereditary spastic paraplegia (HSP): Expanding the phenotypic spectrum of NMNAT1 variants” [Neuromuscular Disorders, 33(2023) 295-301] Sadr, Zahra

35 C p. e1
artikel
3 Crossover randomized controlled trial of bumetanide to rescue an attack of exercise induced hand weakness in hypokalaemic periodic paralysis Scalco, Renata Siciliani

35 C p. 33-38
artikel
4 Editorial Board
35 C p. IFC
artikel
5 Emergencies in Neuromuscular Disorders Quinlivan, Rosaline

35 C p. 25
artikel
6 ENMC Themed Call 2023-2024 Announcement
35 C p. I
artikel
7 Impact of gastrointestinal and urological symptoms in children with myotonic dystrophy type 1 Maagdenberg, Sandra J.M.

35 C p. 1-7
artikel
8 Meeting report: The 2023 FSHD International Research Congress Arjomand, Jamshid

35 C p. 53-57
artikel
9 “MUSCLE BIOPSY” - Its 50th anniversary to this year Goebel, Hans H.

35 C p. 27-28
artikel
10 Neurodiversity, treatment compliance and survival in adults with Duchenne muscular dystrophy: a single-centre retrospective cohort review Nart, Luca

35 C p. 13-18
artikel
11 Neuropathic pain Enax-Krumova Jun.-Prof. Dr. med. Neurologist and pain specialist, Elena

35 C p. 26
artikel
12 Neutral lipid storage disease with myopathy: clinicopathological and genetic features of nine Iranian patients Shahriyari, Hamed

35 C p. 19-24
artikel
13 Response to: The use of guidelines to assess the risk of malignant hyperthermia in individuals with a RYR1 variant Herdewyn, S.

35 C p. 39
artikel
14 The myotubular and centronuclear myopathy patient registry: a multifunctional tool for translational research Bullivant, Joanne

35 C p. 42-52
artikel
15 The use of guidelines to assess the risk of malignant hyperthermia in individuals with an RYR1 variant Voermans, N.C.

35 C p. 40-41
artikel
16 Variants in tropomyosins TPM2 and TPM3 causing muscle hypertonia Wallgren-Pettersson, Carina

35 C p. 29-32
artikel
17 WMS 2024 Congress Flyer
35 C p. II
artikel
18 WMS 2024 Congress information
35 C p. III
artikel
19 WMS General Information
35 C p. IV
artikel
                             19 gevonden resultaten
 
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