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Current Opinion in Neurology, ISSN 1350-7540, 2016, Volume 29, Issue 5, pp. 635 - 641
Purpose of reviewThe aim of the study was to describe the clinical spectrum of limb girdle muscular dystrophies (LGMDs), the pitfalls of the current... 
Therapy | Limb girdle muscular dystrophy | Classification | therapy | PHENOTYPES | MUSCLE MRI FINDINGS | PREVALENCE | MYOPATHY | classification | limb girdle muscular dystrophy | NEUROSCIENCES | EXERCISE | CLINICAL NEUROLOGY | CARDIAC INVOLVEMENT | MUTATION | DYSFERLINOPATHY | LGMD2A | EXPRESSION
Journal Article
Pattern Recognition, ISSN 0031-3203, 02/2019, Volume 86, pp. 368 - 375
Journal Article
Nervno-Myšečnye Bolezni, ISSN 2222-8721, 02/2015, Issue 1, pp. 6 - 20
Congenital muscular dystrophies (CMD) are a large group of genetically determined muscular diseases, initially defined by an early onset before the age of... 
congenital muscular dystrophies | collagenopathies | selenopathies | merosinopathies | laminopathies | dystroglycanopathies
Journal Article
Muscle & Nerve, ISSN 0148-639X, 07/2013, Volume 48, Issue 1, pp. 55 - 67
ABSTRACT Introduction: Glucocorticoid (GC) therapy in Duchenne muscular dystrophy (DMD) has altered disease progression, necessitating contemporary natural... 
phenotype | quality of life/psychology | child/preschool | locomotion | muscular dystrophies/Duchenne/physiopathology | muscle strength/physiology | health status | muscular dystrophies/therapy | respiratory function tests | adolescent | follow‐up studies | adult | humans | male | muscular dystrophies/classification | Humans | Male | Follow-up studies | Child/preschool | Locomotion | Phenotype | Quality of life/psychology | Health status | Muscular dystrophies/Duchenne/physiopathology | Muscular dystrophies/therapy | Muscular dystrophies/classification | Adolescent | Adult | Muscle strength/physiology | Respiratory function tests | PROFILES | DESIGN | 6-MINUTE WALK TEST | RELIABILITY | CLINICAL NEUROLOGY | psychology | Duchenne | muscular dystrophies | PREDNISONE THERAPY | GAIT | therapy | physiology | MUSCULAR-DYSTROPHY | STRENGTH | classification | NEUROSCIENCES | muscle strength | follow-up studies | physiopathology | BOYS | preschool | STAR AMBULATORY ASSESSMENT | quality of life | child | Outcome Assessment (Health Care) - methods | Glucocorticoids - therapeutic use | Prospective Studies | Child, Preschool | Diagnostic Techniques, Neurological - standards | Muscular Dystrophy, Duchenne - epidemiology | Young Adult | Biomedical Research - methods | Clinical Trials as Topic - standards | Child | Cross-Sectional Studies | Muscular Dystrophy, Duchenne - drug therapy | Treatment Outcome | International Cooperation | Disease Progression | Outcome Assessment (Health Care) - standards | Clinical Trials as Topic - methods | Longitudinal Studies | Biomedical Research - standards | Cohort Studies | Muscle Strength - physiology | Muscular Dystrophy, Duchenne - diagnosis | Clinical trials | Medicine, Experimental | Medical research | Corticosteroids | Steroids | Neurologi | Pediatrics | strength | Pediatrik | prednisone therapy | reliability | profiles | boys | 6-minute walk test | Neurology | protocol | children | muscular-dystrophy | star ambulatory assessment
Journal Article
Muscle & Nerve, ISSN 0148-639X, 07/2013, Volume 48, Issue 1, pp. 32 - 54
Journal Article
Muscle & Nerve, ISSN 0148-639X, 06/2017, Volume 55, Issue 6, pp. 810 - 818
Journal Article