Détail de la revue
Documents disponibles dans cette revue
trié(s) par (Pertinence décroissant(e), Date de parution décroissant(e), Date de parution décroissant(e), Système de projection du document croissant(e)) | Mettre toutes les notices dans le panier | Faire une suggestion | Ajouter un critère de recherche
Ocular myasthenia gravis: updates on an elusive target
Melson AT, McClelland CM, Lee MS
Current opinion in neurology, 2019
Emery-Dreifuss muscular dystrophy: focal point nuclear envelope
Muchir A, Worman HJ
Current opinion in neurology, 2019, 32, 5, p 728
Update in Duchenne and Becker muscular dystrophy
Waldrop MA, Flanigan KM
Current opinion in neurology, 2019, 32, 5, p 722
Advances in primary mitochondrial myopathies
de Barcelos IP, Emmanuele V, Hirano M
Current opinion in neurology, 2019, 32, 5, p 715
Charcot-Marie-Tooth disease and related disorders: an evolving landscape
Laura M, Pipis M, Rossor AM, et al.
Current opinion in neurology, 2019, 32, 5, p 641
The congenital myasthenic syndromes: expanding genetic and phenotypic spectrums and refining treatment strategies
Vanhaesebrouck AE, Beeson D
Current opinion in neurology, 2019, 32, 5, p 696
Myasthenia gravis: from autoantibodies to therapy
Mantegazza R, Bernasconi P, Cavalcante P
Current opinion in neurology, 2018, 31, 5, p 517
Malignant hyperthermia: still an issue for neuromuscular diseases?
De Wel B, De Wel B, Claeys KG
Current opinion in neurology, 2018, 31, 5, p 628
How useful is muscle ultrasound in the diagnostic workup of neuromuscular diseases?
van Alfen N, van Alfen N, Gijsbertse K, et al.
Current opinion in neurology, 2018, 31, 5, p 568
Exercise in muscle disorders: what is our current state?
Preisler N, Preisler N, Orngreen MC
Current opinion in neurology, 2018, 31, 5, p 610
Bones and muscular dystrophies: what do we know?
Wood CL, Wood CL, Straub V
Current opinion in neurology, 2018, 31, 5, p 583
Respiratory involvement in neuromuscular disorders
Boentert M, Wenninger S, Sansone VA
Current opinion in neurology, 2017, 30, 5, p 529
New developments in Charcot-Marie-Tooth neuropathy and related diseases
Pareyson D, Saveri P, Pisciotta C
Current opinion in neurology, 2017, 30, 5, p 471
Sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance
Uruha A, Benveniste O
Current opinion in neurology, 2017, 30, 5, p 457
Update on diagnostics of metabolic myopathies
Toscano A, Barca E, Musumeci O
Current opinion in neurology, 2017, 30, 5, p 553
Palliative care in neuromuscular diseases
de Visser M, Oliver DJ
Current opinion in neurology, 2017, 30, 6, p 686
Neuromuscular problems in the ICU
Damian MS, Srinivasan R
Current opinion in neurology, 2017, 30, 5, p 538
Update on new muscle glycogenosis
Laforêt P, Malfatti E, Vissing J
Current opinion in neurology, 2017, 30, 5, p 449
The rapid evolution of molecular genetic diagnostics in neuromuscular diseases
Volk AE, Kubisch C
Current opinion in neurology, 2017, 30, 5, p 523
Integrating clinical and genetic observations in facioscapulohumeral muscular dystrophy
Mul K, van den Boogaard ML, van der Maarel SM, et al.
Current opinion in neurology, 2016, 29, 5, p 606
New aspects of myofibrillar myopathies
Kley RA, Olivé M, Schröder R
Current opinion in neurology, 2016, 29, 5, p 628
Congenital myasthenic syndromes: recent advances
Beeson D
Current opinion in neurology, 2016, 29, 5, p 565
Limb girdle muscular dystrophies: classification, clinical spectrum and emerging therapies
Vissing J
Current opinion in neurology, 2016, 29, 5, p 635
Advances in serological diagnostics of inflammatory myopathies
Benveniste O, Stenzel W, Allenbach Y
Current opinion in neurology, 2016, 29, 5, p 662
