Mots-clés
 > MYOBASE > INFORMATION-COMMUNICATION > type de document > revue de la littérature
revue de la littérature
Commentaire :
Document comprenant une bibliographie exhaustive avec commentaire développé du sujet traité. (26/06/2007)
Synonyme(s)review of the literature reviews |
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 rechercheEtendre la recherche sur niveau(x) vers le bas
Life expectancy at birth in Duchenne muscular dystrophy: a systematic review and meta-analysis
Landfeldt E, Thompson R, Sejersen T, et al.
European journal of epidemiology, 2020
Severe Ocular Complications After Blepharoptosis Correction in the Oculopharyngeal Muscular Dystrophy Patient: Literature Review and Case Presentation
Lin TY, Chen AD, Chang CH, et al.
Annals of plastic surgery, 2020, 84, suppl 1
The validity and utility of the Cutaneous Disease Area and Severity Index (CDASI) as a clinical outcome instrument in dermatomyositis: A comprehensive review
Ahmed S, Chen KL, Werth VP
Seminars in arthritis and rheumatism, 2020
Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD): case reports and epidemiology of ETFDH gene mutations
Chen W, Zhang Y, Ni Y, et al.
BMC neurology, 2019, 19, 1, p 330
Cognitive performance of children with spinal muscular atrophy: A systematic review
Polido GJ, de Miranda MMV, Carvas N, et al.
Dementia & neuropsychologia, 2019, 13, 4, p 436
Cardiovascular complications in patients with idiopathic inflammatory myopathies: does heart matter in idiopathic inflammatory myopathies?
Opinc AH, Makowski MA, Lukasik ZM, et al.
Heart failure reviews, 2019
Significance of Asymptomatic Hyper Creatine-Kinase Emia
Finsterer J, Scorza FA, Scorza CA
Journal of clinical neuromuscular disease, 2019, 21, 2, p 90
The Effectiveness and Value of Treatments for Spinal Muscular Atrophy
Pearson SD, Thokala P, Stevenson M, et al.
Journal of managed care & specialty pharmacy, 2019, 25, 12, p 1300
Characterizing health state utilities associated with Duchenne muscular dystrophy: a systematic review
Szabo SM, Audhya IF, Malone DC, et al.
Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation, 2019
The neuro-ophthalmology of inherited myopathies
Watson E, Ahmad K, Fraser CL
Current opinion in ophthalmology, 2019, 30, 6, p 476
Measuring walking-related performance fatigability in clinical practice: a systematic review
Van Geel F, Moumdjian L, Lamers I, et al.
European journal of physical and rehabilitation medicine, 2019
Quality of life in refractory generalized myasthenia gravis: A rapid review of the literature
Garzon-Orjuela N, van der Werf L, Prieto-Pinto LC, et al.
Intractable & rare diseases research, 2019, p 231
The Utility and Practice of Electrodiagnostic Testing in the Pediatric Population: An AANEM Consensus Statement
Kang PB, McMillan HJ, Kuntz NL, et al.
Muscle & Nerve, 2019
Biologic therapy in the idiopathic inflammatory myopathies
Khoo T, Limaye V
Rheumatology international, 2019
A review of accelerometer-derived physical activity in the idiopathic inflammatory myopathies
Oldroyd A, Little MA, Dixon W, et al.
BMC rheumatology, 2019, 3, p 41
The Effect of Inspiratory Muscle Training on Duchenne Muscular Dystrophy: A Meta-analysis
Williamson E, Pederson N, Rawson H, et al.
Pediatric physical therapy : the official publication of the Section on Pediatrics of the American Physical Therapy Association, 2019, 31, 4, p 323
Motor activity and Becker's muscular dystrophy: lights and shadows
Lanza G, Pino M, Fisicaro F, et al.
The Physician and sportsmedicine, 2019
Efficacy and tolerability of subcutaneously administered immunoglobulin in myasthenia gravis: A systematic review
Adiao KJB, Espiritu AI, Roque VLA, et al.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2019
Incidence and prevalence of vaccine preventable infections in adult patients with autoimmune inflammatory rheumatic diseases (AIIRD): a systemic literature review informing the 2019 update of the EULAR recommendations for vaccination in adult patients with AIIRD
Furer V, Rondaan C, Heijstek M, et al.
RMD open, 2019, 5, 2
Respiratory muscle training in children and adults with neuromuscular disease.
Silva IS, Pedrosa R, Azevedo IG, et al.
The Cochrane database of systematic reviews, 2019, 9
Juvenile dermatomyositis: advances in clinical presentation, myositis-specific antibodies and treatment
Wu JQ, Lu MP, Reed AM
World journal of pediatrics : WJP, 2019
Affective symptoms and apathy in myotonic dystrophy type 1 a systematic review and meta-analysis
van der Velden BG, Okkersen K, Kessels RP, et al.
Journal of affective disorders, 2019, 250, p 260
Defining Features of Patients who Develop Takotsubo Cardiomyopathy during Myasthenic Crisis: A Systematic Review of Case Studies
Kariyanna PT, Sutarjono B, Jayarangaiah A, et al.
American journal of medical case reports, 2019, 7, 9, p 203
Unraveling the role of ectopic thymic tissue in patients undergoing thymectomy for myasthenia gravis
Li F, Tao Y, Bauer G, et al.
Journal of thoracic disease, 2019, 11, 9
MicroRNAs in hereditary and sporadic premature aging syndromes and other laminopathies
Frankel D, Delecourt V, Harhouri K, et al.
Aging cell, 2018
