Pages that link to "Q37394678"

The following pages link to Joint hypermobility as a distinctive feature in the differential diagnosis of myopathies. (Q37394678):

Displaying 15 items.

• Ehlers-danlos syndrome, hypermobility type: an underdiagnosed hereditary connective tissue disorder with mucocutaneous, articular, and systemic manifestations (Q22305374) (← links)
• Approach to the diagnosis of congenital myopathies (Q26999314) (← links)
• Neurological manifestations of Ehlers-Danlos syndrome(s): A review (Q28088448) (← links)
• Ligament-derived matrix stimulates a ligamentous phenotype in human adipose-derived stem cells (Q34165801) (← links)
• The collagen VI-related myopathies Ullrich congenital muscular dystrophy and Bethlem myopathy (Q34178677) (← links)
• Anesthetic Management of a Patient With Ehlers-Danlos Syndrome (Q37505059) (← links)
• The collagen VI-related myopathies: muscle meets its matrix (Q37555710) (← links)
• The neuromuscular differential diagnosis of joint hypermobility (Q38395355) (← links)
• The wrong end of the telescope: neuromuscular mimics of movement disorders (and vice versa). (Q38769259) (← links)
• Anaesthesia Management and Use of Sugammadex in a Patient with Ullrich's Disease (Q42200748) (← links)
• A novel TaqI polymorphism in the coding region of the ovine TNXB gene in the MHC class III region: morphostructural and physiological influences (Q46978533) (← links)
• Myopathy in a 20-year-old female patient with D4ST-1 deficient Ehlers-Danlos syndrome due to a homozygous CHST14 mutation. (Q53805152) (← links)
• Re-writing the natural history of pain and related symptoms in the joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type. (Q53864616) (← links)
• Clinical and genetic findings in a large cohort of patients with ryanodine receptor 1 gene-associated myopathies (Q57334263) (← links)
• The clinical spectrum and genetic variability of limb-girdle muscular dystrophy in a cohort of Chinese patients (Q58782428) (← links)