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Diagnosis, natural history, and management in vascular Ehlers–Danlos syndrome

American journal of medical genetics. Part C, Seminars in medical genetics, 2017-03, Vol.175 (1), p.40-47

2017

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Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type

Genetics in medicine, 2010-10, Vol.12 (10), p.597-605

2010

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The evidence‐based rationale for physical therapy treatment of children, adolescents, and adults diagnosed with joint hypermobility syndrome/hypermobile Ehlers Danlos syndrome

American journal of medical genetics. Part C, Seminars in medical genetics, 2017-03, Vol.175 (1), p.158-167

2017

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Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield

European journal of human genetics : EJHG, 2023-07, Vol.31 (7), p.749-760

2023

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Joint Hypermobility Syndrome: Recognizing a Commonly Overlooked Cause of Chronic Pain

The American journal of medicine, 2017-06, Vol.130 (6), p.640-647

2017

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Thoracic Aortic Aneurysm and Dissection

Journal of the American College of Cardiology, 2014-10, Vol.64 (16), p.1725-1739

2014

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Cardiovascular autonomic dysfunction in Ehlers–Danlos syndrome—Hypermobile type

American journal of medical genetics. Part C, Seminars in medical genetics, 2017-03, Vol.175 (1), p.168-174

2017

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Contemporary approach to joint hypermobility and related disorders

Current opinion in pediatrics, 2017-12, Vol.29 (6), p.640-649

2017

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Hypermobility spectrum disorders and active migraine in Israeli adolescents: A nationwide study

Headache, 2023-07, Vol.63 (7), p.934-941

2023

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Assessment of the beliefs, needs, and expectations for genetic counseling of patients with hypermobile Ehlers‐Danlos syndrome

American journal of medical genetics. Part A, 2022-11, Vol.188 (11), p.3172-3183

2022

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Are patients with hypermobile Ehlers–Danlos syndrome or hypermobility spectrum disorder so different?

Rheumatology international, 2021-10, Vol.41 (10), p.1785-1794

2021

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ATP7A-related copper transport diseases-emerging concepts and future trends

Nature reviews. Neurology, 2011-01, Vol.7 (1), p.15

Kaler, Stephen G

2011

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Diagnosis and treatment of the Ehlers-Danlos syndromes in China: synopsis of the first guidelines

Orphanet journal of rare diseases, 2024-05, Vol.19 (1), p.194-194

2024

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Recognizing and Effectively Managing Hypermobility-Related Conditions

Physical therapy, 2019-09, Vol.99 (9), p.1189-1200

2019

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Mast cell activation and nutritional disorders in patients with hypermobility

Current opinion in gastroenterology, 2024-05, Vol.40 (3), p.225

2024

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Initial description and evaluation of EDS ECHO: An international effort to improve care for people with the Ehlers‐Danlos syndromes and hypermobility spectrum disorders

American journal of medical genetics. Part C, Seminars in medical genetics, 2021-12, Vol.187 (4), p.609-615

2021

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Psychological interventions to improve pain, fatigue, anxiety, depression, and quality of life in children and adults with hypermobility spectrum disorders and Ehlers-Danlos syndrome: a systematic review

Rheumatology international, 2024-01, Vol.44 (1), p.41-55

2024

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Spontaneous Cervical Artery Dissection in Vascular Ehlers-Danlos Syndrome: A Cohort Study

Stroke (1970), 2021-05, Vol.52 (5), p.1628-1635

2021

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Treating pain in patients with Ehlers–Danlos syndrome: Multidisciplinary management of a multisystemic disease

Schmerz (Berlin, Germany), 2024-02, Vol.38 (1), p.12-18

2024

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Vascular Ehlers-Danlos Syndrome: Long-Term Observational Study

Journal of the American College of Cardiology, 2019-04, Vol.73 (15), p.1948-1957

2019

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Ehlers-Danlos syndrome type IV

Orphanet journal of rare diseases, 2007-07, Vol.2 (1), p.32-32, Article 32

Germain, Dominique P

2007

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Pain management in the Ehlers–Danlos syndromes

American journal of medical genetics. Part C, Seminars in medical genetics, 2017-03, Vol.175 (1), p.212-219

2017

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Healthcare utilization among youth with Ehlers–Danlos syndrome hypermobile type

American journal of medical genetics. Part A, 2022-04, Vol.188 (4), p.1109-1117

2022

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Quality of life, unmet needs, and iatrogenic injuries in rehabilitation of patients with Ehlers-Danlos Syndrome hypermobility type/Joint Hypermobility Syndrome

American journal of medical genetics. Part A, 2016-08, Vol.170A (8), p.2044-2051

2016

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Physical therapy treatment of hypermobile Ehlers–Danlos syndrome: A systematic review

American journal of medical genetics. Part A, 2021-10, Vol.185 (10), p.2986-2994

2021

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Diagnosis, natural history, and management in vascular Ehlers–Danlos syndrome

Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type

The evidence‐based rationale for physical therapy treatment of children, adolescents, and adults diagnosed with joint hypermobility syndrome/hypermobile Ehlers Danlos syndrome

Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield

Joint Hypermobility Syndrome: Recognizing a Commonly Overlooked Cause of Chronic Pain

Thoracic Aortic Aneurysm and Dissection

Cardiovascular autonomic dysfunction in Ehlers–Danlos syndrome—Hypermobile type

Contemporary approach to joint hypermobility and related disorders

Hypermobility spectrum disorders and active migraine in Israeli adolescents: A nationwide study

Assessment of the beliefs, needs, and expectations for genetic counseling of patients with hypermobile Ehlers‐Danlos syndrome

Are patients with hypermobile Ehlers–Danlos syndrome or hypermobility spectrum disorder so different?

ATP7A-related copper transport diseases-emerging concepts and future trends

Diagnosis and treatment of the Ehlers-Danlos syndromes in China: synopsis of the first guidelines

Recognizing and Effectively Managing Hypermobility-Related Conditions

Mast cell activation and nutritional disorders in patients with hypermobility

Initial description and evaluation of EDS ECHO: An international effort to improve care for people with the Ehlers‐Danlos syndromes and hypermobility spectrum disorders

Psychological interventions to improve pain, fatigue, anxiety, depression, and quality of life in children and adults with hypermobility spectrum disorders and Ehlers-Danlos syndrome: a systematic review

Spontaneous Cervical Artery Dissection in Vascular Ehlers-Danlos Syndrome: A Cohort Study

Treating pain in patients with Ehlers–Danlos syndrome: Multidisciplinary management of a multisystemic disease

Vascular Ehlers-Danlos Syndrome: Long-Term Observational Study

Ehlers-Danlos syndrome type IV

Pain management in the Ehlers–Danlos syndromes

Healthcare utilization among youth with Ehlers–Danlos syndrome hypermobile type

Quality of life, unmet needs, and iatrogenic injuries in rehabilitation of patients with Ehlers-Danlos Syndrome hypermobility type/Joint Hypermobility Syndrome

Physical therapy treatment of hypermobile Ehlers–Danlos syndrome: A systematic review

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