Pages that link to "Q37552615"
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The following pages link to Consensus statement on standard of care for congenital muscular dystrophies (Q37552615):
Displaying 50 items.
- Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategies (Q22001192) (← links)
- Mechanical insufflation-exsufflation for people with neuromuscular disorders (Q24201568) (← links)
- Respiratory assessment in centronuclear myopathies (Q26864621) (← links)
- Quality improvement in neurology: muscular dystrophy quality measures (Q27348818) (← links)
- Congenital muscular dystrophies: a brief review (Q28255519) (← links)
- Mutations in INPP5K, Encoding a Phosphoinositide 5-Phosphatase, Cause Congenital Muscular Dystrophy with Cataracts and Mild Cognitive Impairment (Q30032671) (← links)
- Assessment of target enrichment platforms using massively parallel sequencing for the mutation detection for congenital muscular dystrophy (Q30455033) (← links)
- Diagnostic approach to the congenital muscular dystrophies (Q30767612) (← links)
- Improving Reproducibility of Phenotypic Assessments in the DyW Mouse Model of Laminin-α2 Related Congenital Muscular Dystrophy (Q33787898) (← links)
- Pneumothoraces in collagen VI-related dystrophy: a case series and recommendations for management. (Q33828542) (← links)
- Neurology of inherited glycosylation disorders (Q34269429) (← links)
- Dystromirs as serum biomarkers for monitoring the disease severity in Duchenne muscular Dystrophy (Q35055089) (← links)
- Nutritional practices at a glance: spinal muscular atrophy type I nutrition survey findings (Q35101826) (← links)
- Reliability and validity of the TIMPSI for infants with spinal muscular atrophy type I (Q35238315) (← links)
- ColVI myopathies: where do we stand, where do we go? (Q35290709) (← links)
- Understanding the experiences and needs of individuals with Spinal Muscular Atrophy and their parents: a qualitative study (Q35820766) (← links)
- Hospitalizations and emergency room visits for adolescents and young adults with muscular dystrophy living in South Carolina (Q35931632) (← links)
- Natural history of pulmonary function in collagen VI-related myopathies (Q37383472) (← links)
- Results of a two-year pilot study of clinical outcome measures in collagen VI- and laminin alpha2-related congenital muscular dystrophies (Q37446660) (← links)
- The collagen VI-related myopathies: muscle meets its matrix (Q37555710) (← links)
- Consensus statement on standard of care for congenital myopathies (Q37585735) (← links)
- Orthopedic Management of Scoliosis by Garches Brace and Spinal Fusion in SMA Type 2 Children (Q37589766) (← links)
- Rate of oral intake and effects of mechanical insufflation-exsufflation on pulmonary complications in patients with duchenne muscular dystrophy (Q37714767) (← links)
- A review of pediatric palliative care service utilization in children with a progressive neuromuscular disease who died on a palliative care program (Q37996979) (← links)
- Ullrich congenital muscular dystrophy: clinicopathological features, natural history and pathomechanism(s). (Q38221009) (← links)
- Pulmonary Manifestations of Neuromuscular Diseases (Q38551822) (← links)
- Domiciliary noninvasive positive airway pressure therapy in children (Q38668436) (← links)
- Clinical course of growth in patients with congenital neuromuscular disease in a single multidisciplinary neuromuscular clinic (Q38769729) (← links)
- Upper extremity outcome measures for collagen VI-related myopathy and LAMA2-related muscular dystrophy (Q38770619) (← links)
- Young adults' experiences of living with recessive limb-girdle muscular dystrophy from a salutogenic orientation: an interview study (Q39061103) (← links)
- Adherence and barriers to hyperinsufflation in children with congenital muscular dystrophy. (Q39164057) (← links)
- Comparison of sitting and supine forced vital capacity in collagen VI-related dystrophy and laminin α2-related dystrophy. (Q40381994) (← links)
- Do abdominal cutouts in thoracolumbosacral orthoses increase pulmonary function? (Q41868817) (← links)
- Hemodynamic instability during prone spine surgery in a patient with merosin-deficient congenital muscular dystrophy (Q44604971) (← links)
- Pediatric laminopathies: Whole-body magnetic resonance imaging fingerprint and comparison with Sepn1 myopathy. (Q45952742) (← links)
- Genetic and Clinical Advances of Congenital Muscular Dystrophy (Q46563168) (← links)
- Cardiac manifestations of congenital LMNA-related muscular dystrophy in children: three case reports and recommendations for care. (Q46953467) (← links)
- Physical therapy services received by individuals with spinal muscular atrophy (SMA). (Q47859543) (← links)
- A new self-report quality of life questionnaire for children with neuromuscular disorders: presentation of the instrument, rationale for its development, and some preliminary results (Q48113030) (← links)
- "3 . . 2 . . 1 . . Impact [factor]: target [academic career] destroyed!": just another statistical casualty (Q50547421) (← links)
- Utility of next generation sequencing in genetic diagnosis of early onset neuromuscular disorders. (Q50967429) (← links)
- Novel Variants in Individuals with RYR1-Related Congenital Myopathies: Genetic, Laboratory, and Clinical Findings. (Q52647770) (← links)
- Amelioration of Muscle and Nerve Pathology in LAMA2 Muscular Dystrophy by AAV9-Mini-Agrin. (Q54210538) (← links)
- Duchenne and Becker muscular dystrophy in adolescents: current perspectives. (Q54918633) (← links)
- Correlation of phenotype with genotype and protein structure in RYR1-related disorders (Q58696990) (← links)
- A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: a Case report (Q60908834) (← links)
- Palliative care services in families of males with muscular dystrophy: Data from MD STARnet (Q64115587) (← links)
- Muscular dystrophies (Q86291937) (← links)
- Dysphagia and Dysarthria in Children with Neuromuscular Diseases, a Prevalence Study (Q90356107) (← links)
- Cough augmentation techniques for people with chronic neuromuscular disorders (Q94400175) (← links)