Mots-clés
![]() étude rétrospectiveSynonyme(s)recherche rétrospective ;retrospective searching ;retrospective study retrospective studies |



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Is prophylactic formal fusion with implant revision necessary in non-ambulatory children with spinal muscular atrophy and growing rods who are no longer lengthened?
Hanna R, Sharafinski M, Patterson K, et al.
Spine deformity, 2020, 8, 3, p 547
Revue : Spine deformity, 8, 3 Titre : Is prophylactic formal fusion with implant revision necessary in non-ambulatory children with spinal muscular atrophy and growing rods who are no longer lengthened? Type de document : Article Auteurs : Hanna R ; Sharafinski M ; Patterson K ; Noonan KJ ; Sund S ; Schultz M ; Schroth MK ; Hetzel S ; Halanski MA Editeur : England Année de publication : 06/2020 Pages : p 547 Langues : Anglais (eng) Mots-clés : amyotrophie spinale ; amyotrophie spinale proximale liée à SMN1 ; chirurgie ; déviation rachidienne ; enfant ; étude rétrospective Pubmed / DOI : Pubmed : 32096140 / DOI : 10.1007/s43390-020-00077-6
N° Profil MNM : 2020022 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32096140 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Emerging PD-1 and PD-1L inhibitors-associated myopathy with a characteristic histopathological pattern
Matas-Garcia A, Milisenda JC, Selva-O'Callaghan A, et al.
Autoimmunity reviews, 2020, 19, 2
Revue : Autoimmunity reviews, 19, 2 Titre : Emerging PD-1 and PD-1L inhibitors-associated myopathy with a characteristic histopathological pattern Type de document : Article Auteurs : Matas-Garcia A ; Milisenda JC ; Selva-O'Callaghan A ; Prieto-Gonzalez S ; Padrosa J ; Cabrera C ; Reguart N ; Castrejon N ; Sole M ; Ros J ; Trallero-Araguas E ; Antoniol MN ; Vila-Pijoan G ; Grau JM Editeur : Netherlands Année de publication : 02/2020 Langues : Anglais (eng) Mots-clés : effet indésirable ; étude rétrospective ; inhibiteur du point de contrôle immunitaire ; maladie neuromusculaire ; myopathie inflammatoire Pubmed / DOI : Pubmed : 31838162 / DOI : 10.1016/j.autrev.2019.102455
N° Profil MNM : 2019122 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/31838162 Voir aussiAvis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Hypoglycemia in patients with congenital muscle disease
Hayes LH, Yun P, Mohassel P, et al.
BMC Pediatrics, 2020, 20, 1, p 57
Revue : BMC Pediatrics, 20, 1 Titre : Hypoglycemia in patients with congenital muscle disease Type de document : Article Auteurs : Hayes LH ; Yun P ; Mohassel P ; Norato G ; Donkervoort S ; Leach ME ; Alvarez R ; Rutkowski A ; Shaw ND ; Foley AR ; Bonnemann CG Editeur : England Année de publication : 02/2020 Pages : p 57 Langues : Anglais (eng) Mots-clés : dystrophie musculaire congénitale ; enfant ; épidémiologie ; étude rétrospective ; hypoglycémie ; maladie neuromusculaire ; myopathie congénitale Pubmed / DOI : Pubmed : 32028919 / DOI : 10.1186/s12887-020-1909-5
N° Profil MNM : 2020021 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32028919 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Early NIV is associated with accelerated lung function decline in Duchenne muscular dystrophy treated with glucocorticosteroids
Angliss ME, Sclip KD, Gauld L
BMJ open respiratory research, 2020, 7, 1
Revue : BMJ open respiratory research, 7, 1 Titre : Early NIV is associated with accelerated lung function decline in Duchenne muscular dystrophy treated with glucocorticosteroids Type de document : Article Auteurs : Angliss ME ; Sclip KD ; Gauld L Année de publication : 02/2020 Langues : Anglais (eng) Mots-clés : adolescent ; dystrophie musculaire de Duchenne ; étude de cohorte ; étude rétrospective ; respiration (macroscopique) ; stéroïde ; ventilation non invasive Pubmed / DOI : Pubmed : 32079608 / DOI : 10.1136/bmjresp-2019-000517
N° Profil MNM : 2020022 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32079608 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Transforaminal lumbar puncture for intrathecal access: Case series with literature review and comparison to other techniques
Velayudhan V, Patel S, Danziger A, et al.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2020, 72, p 114
Revue : Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 72 Titre : Transforaminal lumbar puncture for intrathecal access: Case series with literature review and comparison to other techniques Type de document : Article Auteurs : Velayudhan V ; Patel S ; Danziger A ; Grigorian A ; Waite S ; Efendizade A Editeur : Scotland Année de publication : 02/2020 Pages : p 114 Langues : Anglais (eng) Mots-clés : amyotrophie spinale ; amyotrophie spinale proximale (type II) ; amyotrophie spinale proximale liée à SMN1 ; étude rétrospective ; maladie du motoneurone ; maladie neuromusculaire ; nusinersen ; thérapie génique ; voie d'administration Pubmed / DOI : Pubmed : 31980274 / DOI : 10.1016/j.jocn.2019.12.056
N° Profil MNM : 2020013 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/31980274 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Improving specialised care for neuromuscular patients reduces the frequency of preventable emergency hospital admissions
Scalco RS, Quinlivan RM, Nastasi L, et al.
Neuromuscular disorders : NMD, 2020, p 173
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Risk Factors for Cardiac and Non-cardiac Causes of Death in Males with Duchenne Muscular Dystrophy
Wittlieb-Weber CA, Knecht KR, Villa CR, et al.
Pediatric cardiology, 2020
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Effect of mechanical insufflation-exsufflation in children with neuromuscular weakness
Veldhoen ES, Verweij-van den Oudenrijn LP, Ros LA, et al.
Pediatric pulmonology, 2020, 55, 2, p 510
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Hallazgos urodinamicos en pacientes con enfermedad de Charcot-Marie-Tooth con sintomas del tracto urinario inferior : Urodynamic findings in Charcot-Marie-Tooth patients with lower urinary tract symptoms
Gutierrez Ruiz C, Mateu Arrom L, Mayordomo O, et al.
Actas urologicas espanolas, 2020, 44, 1, p 34
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Airway abnormalities in very early treated infantile-onset Pompe disease: A large-scale survey by flexible bronchoscopy
Yang CF, Niu DM, Tai SK, et al.
American Journal of Medical Genetics Part A, 2020
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Statin-induced anti-HMGCR myopathy: successful therapeutic strategies for corticosteroid-free remission in 55 patients
Meyer A, Troyanov Y, Drouin J, et al.
Arthritis research & therapy, 2020, 22, 1, p 5
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Anti-RNP antibodies delineate a subgroup of myositis: A systematic retrospective study on 46 patients
Wesner N, Uruha A, Suzuki S, et al.
Autoimmunity reviews, 2020
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Higher dosing of alglucosidase alfa improves outcomes in children with Pompe disease: a clinical study and review of the literature
Khan AA, Case LE, Herbert M, et al.
Genetics in medicine : official journal of the American College of Medical Genetics, 2020
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Real-world outcomes of long-term prednisone and deflazacort use in patients with Duchenne muscular dystrophy: experience at a single, large care center
Marden JR, Freimark J, Yao Z, et al.
Journal of comparative effectiveness research, 2020
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Relationship between Eating and Digestive Symptoms and Respiratory Function in Advanced Duchenne Muscular Dystrophy Patients
Lee JW, Oh HJ, Choi WA, et al.
Journal of Neuromuscular Diseases, 2020
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Chronic Graft Versus Host Myopathies: Noninflammatory, Multi-Tissue Pathology With Glycosylation Disorders
Pestronk A
Journal of neuropathology and experimental neurology, 2020, 79, 1, p 102
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Bilateral scapulothoracic arthrodesis for facioscapulohumeral muscular dystrophy: function, fusion, and respiratory consequences
Boileau P, Pison A, Wilson A, et al.
Journal of shoulder and elbow surgery, 2020
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Differential response to rituximab in anti-AChR and anti-MuSK positive myasthenia gravis patients: a single-center retrospective study
Litchman T, Roy B, Kumar A, et al.
Journal of the neurological sciences, 2020
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Neurodevelopmental, behavioral, and emotional symptoms common in Duchenne muscular dystrophy
Darmahkasih AJ, Rybalsky I, Tian C, et al.
Muscle & Nerve, 2020
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Charcot-Marie-Tooth disease: experience from a large Italian tertiary neuromuscular center
Gentile L, Russo M, Fabrizi GM, et al.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2020
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Management and current status of spinal muscular atrophy: a retrospective multicentre claims database analysis
Darba J
Orphanet journal of rare diseases, 2020, 15, 1, p 8
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Pulmonary outcome measures in long-term survivors of infantile Pompe disease on enzyme replacement therapy: A case series
Elmallah MK, Desai AK, Nading EB, et al.
Pediatric pulmonology, 2020
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CTG expansion in the DMPK gene: semen quality assessment and outcome of Preimplantation Genetic Diagnosis
Puy V, Mayeur A, Levy A, et al.
The Journal of clinical endocrinology and metabolism, 2020
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ASC-1 Is a Cell Cycle Regulator Associated with Severe and Mild Forms of Myopathy
Villar-Quiles RN, Catervi F, Cabet E, et al.
Annals of neurology, 2019
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Healthcare utilisation in children with SMA type 1 treated with nusinersen: a single centre retrospective review
Ali I, Gilchrist FJ, Carroll WD, et al.
BMJ paediatrics open, 2019, 3, 1
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