Pages that link to "Q37426320"

The following pages link to Congenital muscular dystrophy. Part I: a review of phenotypical and diagnostic aspects (Q37426320):

Displaying 20 items.

• Pharmacology of manipulating lean body mass (Q26824503) (← links)
• Congenital muscular dystrophy: from muscle to brain (Q27023097) (← links)
• Diagnostic approach to the congenital muscular dystrophies (Q30767612) (← links)
• Limb-girdle and congenital muscular dystrophies: current diagnostics, management, and emerging technologies (Q33837536) (← links)
• Congenital muscular dystrophy and generalized epilepsy caused by GMPPB mutations (Q33940640) (← links)
• Comprehensive mutation analysis for congenital muscular dystrophy: a clinical PCR-based enrichment and next-generation sequencing panel (Q34551175) (← links)
• A novel fluorescent assay for T-synthase activity (Q34552242) (← links)
• Air stacking: effects on pulmonary function in patients with spinal muscular atrophy and in patients with congenital muscular dystrophy (Q34679349) (← links)
• Peripheral nerve pathology, including aberrant Schwann cell differentiation, is ameliorated by doxycycline in a laminin-α2-deficient mouse model of congenital muscular dystrophy. (Q35030852) (← links)
• Rigid Spine Syndrome among Children in Oman (Q36009885) (← links)
• Versican processing by a disintegrin-like and metalloproteinase domain with thrombospondin-1 repeats proteinases-5 and -15 facilitates myoblast fusion. (Q36543792) (← links)
• Glia unglued: how signals from the extracellular matrix regulate the development of myelinating glia (Q37915435) (← links)
• Enter the matrix: shape, signal and superhighway. (Q38078500) (← links)
• Common recessive limb girdle muscular dystrophies differential diagnosis: why and how? (Q38253968) (← links)
• Immortalized pathological human myoblasts: towards a universal tool for the study of neuromuscular disorders (Q39738924) (← links)
• Perioperative considerations in Walker-Warburg syndrome. (Q43246617) (← links)
• Rigid spinal muscular dystrophy and rigid spine syndrome: report of 7 children (Q46155174) (← links)
• Comparison of brain MRI findings with language and motor function in the dystroglycanopathies (Q48357459) (← links)
• Cystic kidneys in fetal Walker-Warburg syndrome with POMT2 mutation: Intrafamilial phenotypic variability in four siblings and review of literature. (Q52088286) (← links)
• Myotonic Dystrophy and Developmental Regulation of RNA Processing (Q88453318) (← links)