Ehlers-danlos syndrome, hypermobility type: an underdiagnosed hereditary connective tissue disorder with mucocutaneous, articular, and systemic manifestations
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Neurovisceral phenotypes in the expression of psychiatric symptomsEhlers-Danlos Syndrome, Hypermobility Type: Impact of Somatosensory Orthoses on Postural Control (A Pilot Study)Benign joint hypermobility syndrome in soldiers; what is the effect of military training courses on associated joint instabilities?Pregnancy outcome in joint hypermobility syndrome and Ehlers-Danlos syndrome.Functional adaptation of tendon and skeletal muscle to resistance training in three patients with genetically verified classic Ehlers Danlos Syndrome.Targeted deletion of collagen V in tendons and ligaments results in a classic Ehlers-Danlos syndrome joint phenotype.Transcriptome-Wide Expression Profiling in Skin Fibroblasts of Patients with Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome Hypermobility TypeHealth-related quality of life for children with rare diagnoses, their parents' satisfaction with life and the association between the two.Ehlers-Danlos syndrome hypermobility type is associated with rheumatic diseasesMultimodal chiropractic care of pain and disability for a patient diagnosed with benign joint hypermobility syndrome: a case reportJoint hypermobility syndrome: a review for clinicians.Connective tissue, Ehlers-Danlos syndrome(s), and head and cervical pain.Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy number.The role of narrative medicine in the management of joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type.The association between Ehlers-Danlos syndrome-hypermobility type and gastrointestinal symptoms in university students: a cross-sectional study.Spectrum of mucocutaneous manifestations in 277 patients with joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type.Gastrointestinal disorders in joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type: A review for the gastroenterologist.Hypermobile Ehlers-Danlos syndrome (a.k.a. Ehlers-Danlos syndrome Type III and Ehlers-Danlos syndrome hypermobility type): Clinical description and natural history.Orthopaedic management of the Ehlers-Danlos syndromes.Ehlers-Danlos hypermobility type in an adult with chronic pain and fatigue: a case study.Proprioceptive precision is impaired in Ehlers-Danlos syndrome.Goose skin in a girl with Ehlers-Danlos syndrome.Long-term prognosis of patients with Ehlers-Danlos syndrome and epilepsy.Proprioceptive sensitivity in Ehlers-Danlos syndrome patients.Multimodal Chiropractic Care for Pain and Disability in a Patient Diagnosed With Ehlers-Danlos Syndrome-Hypermobility Type: A Case Report.Identifying lower limb specific and generalised joint hypermobility in adults: validation of the Lower Limb Assessment Score.Dominant Transmission Observed in Adolescents and Families With Orthostatic Intolerance.Functional gastrointestinal disorders are associated with the joint hypermobility syndrome in secondary care: a case-control study.The association between muscle strength and activity limitations in patients with the hypermobility type of Ehlers-Danlos syndrome: the impact of proprioception.The role of the ligamentum teres in the adult hip: redundant or relevant? A review.Visceroptosis and the Ehlers-Danlos Syndrome.The symptom matrix: Using a formalism-based approach to address complex syndromes systematically.Refining patterns of joint hypermobility, habitus, and orthopedic traits in joint hypermobility syndrome and Ehlers-Danlos syndrome, hypermobility type.Joint hypermobility and headache.Re-writing the natural history of pain and related symptoms in the joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type.A study of migraine characteristics in joint hypermobility syndrome a.k.a. Ehlers–Danlos syndrome, hypermobility typeNosology and inheritance pattern(s) of joint hypermobility syndrome and Ehlers-Danlos syndrome, hypermobility type: A study of intrafamilial and interfamilial variability in 23 Italian pedigrees
P2860
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P2860
Ehlers-danlos syndrome, hypermobility type: an underdiagnosed hereditary connective tissue disorder with mucocutaneous, articular, and systemic manifestations
description
2012 nî lūn-bûn
@nan
2012 թուականին հրատարակուած գիտական յօդուած
@hyw
2012 թվականին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Ehlers-danlos syndrome, hyperm ...... r, and systemic manifestations
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Ehlers-danlos syndrome, hyperm ...... r, and systemic manifestations
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Ehlers-danlos syndrome, hyperm ...... r, and systemic manifestations
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Ehlers-danlos syndrome, hyperm ...... r, and systemic manifestations
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type
label
Ehlers-danlos syndrome, hyperm ...... r, and systemic manifestations
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Ehlers-danlos syndrome, hyperm ...... r, and systemic manifestations
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Ehlers-danlos syndrome, hyperm ...... r, and systemic manifestations
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Ehlers-danlos syndrome, hyperm ...... r, and systemic manifestations
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prefLabel
Ehlers-danlos syndrome, hyperm ...... r, and systemic manifestations
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Ehlers-danlos syndrome, hyperm ...... r, and systemic manifestations
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Ehlers-danlos syndrome, hyperm ...... r, and systemic manifestations
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Ehlers-danlos syndrome, hyperm ...... r, and systemic manifestations
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P2860
P3181
P356
P1433
P1476
Ehlers-danlos syndrome, hyperm ...... r, and systemic manifestations
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P2860
P304
P3181
P356
10.5402/2012/751768
P407
P577
2012-01-01T00:00:00Z