Pages that link to "Q37585735"

The following pages link to Consensus statement on standard of care for congenital myopathies (Q37585735):

Displaying 30 items.

• Multidisciplinary approach to the management of myopathies (Q34523022) ‎ (← links)
• Combined MRI and ³¹P-MRS investigations of the ACTA1(H40Y) mouse model of nemaline myopathy show impaired muscle function and altered energy metabolism (Q34684528) ‎ (← links)
• An integrated diagnosis strategy for congenital myopathies. (Q34797333) ‎ (← links)
• Multimodal MRI and (31)P-MRS investigations of the ACTA1(Asp286Gly) mouse model of nemaline myopathy provide evidence of impaired in vivo muscle function, altered muscle structure and disturbed energy metabolism (Q34973774) ‎ (← links)
• Congenital myopathies: Natural history of a large pediatric cohort (Q35106557) ‎ (← links)
• Feeding and Swallowing Disorders in Pediatric Neuromuscular Diseases: An Overview (Q37589746) ‎ (← links)
• Rate of oral intake and effects of mechanical insufflation-exsufflation on pulmonary complications in patients with duchenne muscular dystrophy (Q37714767) ‎ (← links)
• Skeletal muscle α-actin diseases (actinopathies): pathology and mechanisms. (Q38028847) ‎ (← links)
• Managing snoring and obstructive sleep apnoea in childhood (Q38153068) ‎ (← links)
• Insights into the effects of disease-causing mutations in human actins (Q38191504) ‎ (← links)
• Consensus statement on preventive and symptomatic care of leukodystrophy patients (Q38313759) ‎ (← links)
• Pulmonary Manifestations of Neuromuscular Diseases (Q38551822) ‎ (← links)
• A fine balance and a shared learning journey: Exploring healthcare engagement through the experiences of youth with Neuromuscular Disorders. (Q38558959) ‎ (← links)
• A natural history study of X-linked myotubular myopathy (Q38607699) ‎ (← links)
• Clinical course of growth in patients with congenital neuromuscular disease in a single multidisciplinary neuromuscular clinic (Q38769729) ‎ (← links)
• Anesthetic management of 877 pediatric patients undergoing muscle biopsy for neuromuscular disorders: a 20-year review (Q38816760) ‎ (← links)
• Dysphagia in Duchenne muscular dystrophy: practical recommendations to guide management (Q41976150) ‎ (← links)
• Children with central and peripheral neurologic disorders have distinguishable patterns of dysphagia on videofluoroscopic swallow study. (Q45871740) ‎ (← links)
• Pneumonia in pediatric acute neuromuscular respiratory failure (Q46574389) ‎ (← links)
• Congenital myopathies: clinical phenotypes and new diagnostic tools (Q47134873) ‎ (← links)
• Ultrasound of oral and masticatory muscles: Why every neuromuscular swallow team should have an ultrasound machine (Q47252140) ‎ (← links)
• Congenital myopathies: disorders of excitation-contraction coupling and muscle contraction (Q49388884) ‎ (← links)
• Cardiac α-actin over-expression therapy in dominant ACTA1 disease. (Q50937208) ‎ (← links)
• Utility of next generation sequencing in genetic diagnosis of early onset neuromuscular disorders. (Q50967429) ‎ (← links)
• Treating pediatric neuromuscular disorders: The future is now. (Q52756417) ‎ (← links)
• Molecular Genetics of Nemaline Myopathy (Q57394322) ‎ (← links)
• Motor function performance in individuals with RYR1-related myopathies (Q90028044) ‎ (← links)
• Congenital myopathies in the adult neuromuscular clinic: Diagnostic challenges and pitfalls (Q92008119) ‎ (← links)
• KLHL40 Mutation Associated with Severe Nemaline Myopathy, Fetal Akinesia, and Cleft Palate (Q92462397) ‎ (← links)
• Nemaline myopathies: a current view (Q92950622) ‎ (← links)