Ehlers-Danlos syndrome: how to diagnose and when to perform genetic tests. - Wikidata - wikimedia - TriplyDB

Ehlers-Danlos syndrome: how to diagnose and when to perform genetic tests.

Ehlers-Danlos syndrome: how to diagnose and when to perform genetic tests.

http://www.wikidata.org/entity/Q38226265

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Critical involvement of ZEB2 in collagen fibrillogenesis: the molecular similarity between Mowat-Wilson syndrome and Ehlers-Danlos syndrome Nationwide population-based cohort study of psychiatric disorders in individuals with Ehlers-Danlos syndrome or hypermobility syndrome and their siblings A novel missense mutation of COL5A2 in a patient with Ehlers-Danlos syndrome.Ehlers-Danlos syndrome, classical type.Genetics of eosinophilic esophagitis.Systemic Multiple Aneurysms Caused by Vascular Ehlers-Danlos Syndrome.The health and life path of rare disease patients: results of the 2015 French barometer.A multimodal physical therapy approach utilizing the Maitland concept in the management of a patient with cervical and lumbar radiculitis and Ehlers-Danlos syndrome-hypermobility type: A case report.Multiple fractures in infants who have Ehlers-Danlos/hypermobility syndrome and or vitamin D deficiency: A case series of 72 infants whose parents were accused of child abuse and neglect.

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Ehlers-Danlos syndrome: how to diagnose and when to perform genetic tests.

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Archives of Disease in Childhood

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Postural tachycardia syndrome: a heterogeneous and multifactorial disorder

Haploinsufficiency of TNXB is associated with hypermobility type of Ehlers-Danlos syndrome.

Loss of dermatan-4-sulfotransferase 1 function results in adducted thumb-clubfoot syndrome.

A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency.

Loss-of-function mutations of CHST14 in a new type of Ehlers-Danlos syndrome.

Effect of celiprolol on prevention of cardiovascular events in vascular Ehlers-Danlos syndrome: a prospective randomised, open, blinded-endpoints trial.

Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss

Clinical and molecular characterization of 40 patients with classic Ehlers-Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations

The Ehlers-Danlos syndrome, a disorder with many faces.

Addressing the confounding role of joint hypermobility syndrome and gastrointestinal involvement in postural orthostatic tachycardia syndrome.

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Ehlers-Danlos syndrome