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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
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
Hypoglycemia in patients with congenital muscle disease
Hayes LH, Yun P, Mohassel P, et al.
BMC Pediatrics, 2020, 20, 1, p 57
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Neurodevelopmental, behavioral, and emotional symptoms common in Duchenne muscular dystrophy
Darmahkasih AJ, Rybalsky I, Tian C, et al.
Muscle & Nerve, 2020
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
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
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
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
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
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
