Consensus statement on standard of care for congenital muscular dystrophies. - Wikidata - wikimedia - TriplyDB

Consensus statement on standard of care for congenital muscular dystrophies.

Consensus statement on standard of care for congenital muscular dystrophies.

http://www.wikidata.org/entity/Q37552615

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Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategies.Mechanical insufflation-exsufflation for people with neuromuscular disorders Respiratory assessment in centronuclear myopathies Quality improvement in neurology: muscular dystrophy quality measures Congenital muscular dystrophies: a brief review Mutations in INPP5K, Encoding a Phosphoinositide 5-Phosphatase, Cause Congenital Muscular Dystrophy with Cataracts and Mild Cognitive Impairment Assessment of target enrichment platforms using massively parallel sequencing for the mutation detection for congenital muscular dystrophy.Diagnostic approach to the congenital muscular dystrophies.Improving Reproducibility of Phenotypic Assessments in the DyW Mouse Model of Laminin-α2 Related Congenital Muscular Dystrophy.Pneumothoraces in collagen VI-related dystrophy: a case series and recommendations for management.Neurology of inherited glycosylation disorders.Dystromirs as serum biomarkers for monitoring the disease severity in Duchenne muscular Dystrophy.Nutritional practices at a glance: spinal muscular atrophy type I nutrition survey findings.Reliability and validity of the TIMPSI for infants with spinal muscular atrophy type I ColVI myopathies: where do we stand, where do we go?Understanding the experiences and needs of individuals with Spinal Muscular Atrophy and their parents: a qualitative study Hospitalizations and emergency room visits for adolescents and young adults with muscular dystrophy living in South Carolina Natural history of pulmonary function in collagen VI-related myopathies Results of a two-year pilot study of clinical outcome measures in collagen VI- and laminin alpha2-related congenital muscular dystrophies.The collagen VI-related myopathies: muscle meets its matrix.Consensus statement on standard of care for congenital myopathies.Orthopedic Management of Scoliosis by Garches Brace and Spinal Fusion in SMA Type 2 Children.Rate of oral intake and effects of mechanical insufflation-exsufflation on pulmonary complications in patients with duchenne muscular dystrophy.A review of pediatric palliative care service utilization in children with a progressive neuromuscular disease who died on a palliative care program.Ullrich congenital muscular dystrophy: clinicopathological features, natural history and pathomechanism(s).Pulmonary Manifestations of Neuromuscular Diseases.Domiciliary noninvasive positive airway pressure therapy in children.Clinical course of growth in patients with congenital neuromuscular disease in a single multidisciplinary neuromuscular clinic.Upper extremity outcome measures for collagen VI-related myopathy and LAMA2-related muscular dystrophy.Young adults' experiences of living with recessive limb-girdle muscular dystrophy from a salutogenic orientation: an interview study.Adherence and barriers to hyperinsufflation in children with congenital muscular dystrophy.Comparison of sitting and supine forced vital capacity in collagen VI-related dystrophy and laminin α2-related dystrophy.Do abdominal cutouts in thoracolumbosacral orthoses increase pulmonary function?Hemodynamic instability during prone spine surgery in a patient with merosin-deficient congenital muscular dystrophy.Pediatric laminopathies: Whole-body magnetic resonance imaging fingerprint and comparison with Sepn1 myopathy.Genetic and Clinical Advances of Congenital Muscular Dystrophy.Cardiac manifestations of congenital LMNA-related muscular dystrophy in children: three case reports and recommendations for care.Physical therapy services received by individuals with spinal muscular atrophy (SMA).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."3 . . 2 . . 1 . . Impact [factor]: target [academic career] destroyed!": just another statistical casualty.

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Consensus statement on standard of care for congenital muscular dystrophies.

http://www.wikidata.org/entity/Q37552615

description

2010 nî lūn-bûn

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2010年の論文

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年學術文章

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2010年學術文章

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2010年學術文章

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name

Consensus statement on standard of care for congenital muscular dystrophies.

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Consensus statement on standard of care for congenital muscular dystrophies.

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type

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Consensus statement on standard of care for congenital muscular dystrophies.

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Consensus statement on standard of care for congenital muscular dystrophies.

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prefLabel

Consensus statement on standard of care for congenital muscular dystrophies.

@en

Consensus statement on standard of care for congenital muscular dystrophies.

@nl

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Journal of Child Neurology

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Consensus statement on standard of care for congenital muscular dystrophies.

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Ana Ferreiro

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Andrea Vianello

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Brigitte Estournet-Mathiaud

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Caroline Sewry

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Carsten G Bonnemann

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P2860

Walker-Warburg syndrome

Treatment for swallowing difficulties (dysphagia) in chronic muscle disease

Collagen VI related muscle disorders

The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review

Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy

Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study

Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan

Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophy

Sugar-coaters and straight talkers: communicating about developmental delays in primary care.

Pulmonary manifestations of neuromuscular disease with special reference to Duchenne muscular dystrophy and spinal muscular atrophy.

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