Pages that link to "Q38221009"

The following pages link to Ullrich congenital muscular dystrophy: clinicopathological features, natural history and pathomechanism(s). (Q38221009):

Displaying 15 items.

• A TALEN-Exon Skipping Design for a Bethlem Myopathy Model in Zebrafish (Q27301818) ‎ (← links)
• "Target" and "Sandwich" Signs in Thigh Muscles have High Diagnostic Values for Collagen VI-related Myopathies (Q37157908) ‎ (← links)
• Autophagy activation in COL6 myopathic patients by a low-protein-diet pilot trial (Q37520725) ‎ (← links)
• New perspectives on the development of muscle contractures following central motor lesions. (Q38806009) ‎ (← links)
• Physiology of respiratory disturbances in muscular dystrophies. (Q41934825) ‎ (← links)
• Clinical, Pathologic, and Genetic Features of Collagen VI-Related Myopathy in Korea. (Q42646168) ‎ (← links)
• Skin Biopsy for Diagnosis of Ullrich Congenital Muscular Dystrophy: An Observational Study (Q50056255) ‎ (← links)
• Novel Nonsense Mutation in SLC39A13 Initially Presenting as Myopathy: Case Report and Review of the Literature. (Q52624722) ‎ (← links)
• Muscle MRI in pediatrics: clinical, pathological and genetic correlation. (Q52924614) ‎ (← links)
• The Case for Laboratory Developed Procedures: Quality and Positive Impact on Patient Care. (Q53108123) ‎ (← links)
• From Structure to Phenotype: Impact of Collagen Alterations on Human Health. (Q55096200) ‎ (← links)
• Compound heterozygous POMGNT1 mutations leading to muscular dystrophy-dystroglycanopathy type A3: a case report (Q64065905) ‎ (← links)
• Overexpression of miR-29 Leads to Myopathy that Resemble Pathology of Ullrich Congenital Muscular Dystrophy. (Q64974654) ‎ (← links)
• Muscular dystrophies (Q91594164) ‎ (← links)
• Circulating Biomarkers in Muscular Dystrophies: Disease and Therapy Monitoring (Q97423855) ‎ (← links)