Mots-clés
![]() 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 |



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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
Revue : European journal of epidemiology Titre : Life expectancy at birth in Duchenne muscular dystrophy: a systematic review and meta-analysis Type de document : Article Auteurs : Landfeldt E ; Thompson R ; Sejersen T ; McMillan HJ ; Kirschner J ; Lochmuller H Editeur : Netherlands Année de publication : 27/02/2020 Langues : Anglais (eng) Mots-clés : dystrophie musculaire de Duchenne ; espérance de vie ; méta-analyse ; revue de la littérature Pubmed / DOI : Pubmed : 32107739 / DOI : 10.1007/s10654-020-00613-8
N° Profil MNM : 2020022 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32107739 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
Revue : Annals of plastic surgery, 84, suppl 1 Titre : Severe Ocular Complications After Blepharoptosis Correction in the Oculopharyngeal Muscular Dystrophy Patient: Literature Review and Case Presentation Type de document : Article Auteurs : Lin TY ; Chen AD ; Chang CH ; Liang WC ; Minami N ; Nishino I ; Lai CS Editeur : United States Année de publication : 01/2020 Langues : Anglais (eng) Mots-clés : complication chirurgicale ; dystrophie musculaire ; dystrophie musculaire oculopharyngée ; étude de cas ; maladie neuromusculaire ; ptosis ; revue de la littérature Pubmed / DOI : Pubmed : 31833892 / DOI : 10.1097/SAP.0000000000002198
N° Profil MNM : 2019122 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/31833892 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
Revue : Seminars in arthritis and rheumatism Titre : The validity and utility of the Cutaneous Disease Area and Severity Index (CDASI) as a clinical outcome instrument in dermatomyositis: A comprehensive review Type de document : Article Auteurs : Ahmed S ; Chen KL ; Werth VP Editeur : United States Année de publication : 01/2020 Langues : Anglais (eng) Mots-clés : dermatomyosite ; échelle d'évaluation ; efficacité thérapeutique ; myopathie inflammatoire ; qualité de vie ; revue de la littérature Pubmed / DOI : Pubmed : 32057402 / DOI : 10.1016/j.semarthrit.2020.01.002
N° Profil MNM : 2020021 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32057402 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
Revue : BMC neurology, 19, 1 Titre : Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD): case reports and epidemiology of ETFDH gene mutations Type de document : Article Auteurs : Chen W ; Zhang Y ; Ni Y ; Cai S ; Zheng X ; Mastaglia FL ; Wu J Editeur : England Année de publication : 12/2019 Pages : p 330 Langues : Anglais (eng) Mots-clés : adolescent ; Asie ; déficit en acyl-CoA déshydrogénase ; effet fondateur ; épidémiologie ; étude de cas ; lipidose ; maladie métabolique ; maladie neuromusculaire ; masculin ; myopathie mitochondriale liée à ETFDH ; revue de la littérature Pubmed / DOI : Pubmed : 31852447 / DOI : 10.1186/s12883-019-1562-5
N° Profil MNM : 2019122 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/31852447 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
Revue : Dementia & neuropsychologia, 13, 4 Titre : Cognitive performance of children with spinal muscular atrophy: A systematic review Type de document : Article Auteurs : Polido GJ ; de Miranda MMV ; Carvas N ; Mendonça RH ; Caromano FA ; Reed UC ; Zanoteli E ; Voos MC Editeur : Brazil Année de publication : 12/2019 Pages : p 436 Langues : Anglais (eng) Mots-clés : amyotrophie spinale ; amyotrophie spinale proximale liée à SMN1 ; article de synthèse ; cognition ; maladie du motoneurone ; maladie neuromusculaire ; revue de la littérature Pubmed / DOI : Pubmed : 31844498 / DOI : 10.1590/1980-57642018dn13-040011
N° Profil MNM : 2019122 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/31844498 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
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Significance of Asymptomatic Hyper Creatine-Kinase Emia
Finsterer J, Scorza FA, Scorza CA
Journal of clinical neuromuscular disease, 2019, 21, 2, p 90
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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
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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
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The neuro-ophthalmology of inherited myopathies
Watson E, Ahmad K, Fraser CL
Current opinion in ophthalmology, 2019, 30, 6, p 476
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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
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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
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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
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Biologic therapy in the idiopathic inflammatory myopathies
Khoo T, Limaye V
Rheumatology international, 2019
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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
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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
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Motor activity and Becker's muscular dystrophy: lights and shadows
Lanza G, Pino M, Fisicaro F, et al.
The Physician and sportsmedicine, 2019
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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
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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
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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
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Juvenile dermatomyositis: advances in clinical presentation, myositis-specific antibodies and treatment
Wu JQ, Lu MP, Reed AM
World journal of pediatrics : WJP, 2019
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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
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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
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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
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MicroRNAs in hereditary and sporadic premature aging syndromes and other laminopathies
Frankel D, Delecourt V, Harhouri K, et al.
Aging cell, 2018
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