Extracutaneous features and complications of the Ehlers-Danlos syndromes: A systematic review
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N. Burrows | I. Winship | S. Seneviratne | M. Lavallee | I. Hausser | J. Schubart | B. Doolan | F. Michael Pope
[1] N. Burrows,et al. The role of cutaneous manifestations in the diagnosis of the Ehlers‐Danlos syndromes , 2022, Skin health and disease.
[2] G. Larson,et al. Alterations in glycosaminoglycan biosynthesis associated with the Ehlers-Danlos Syndromes. , 2022, American journal of physiology. Cell physiology.
[3] M. Fehlings,et al. Spinal manifestations of Ehlers-Danlos syndrome: a scoping review. , 2022, Journal of neurosurgery. Spine.
[4] R. Wadia. Periodontal Ehlers-Danlos syndrome. , 2020, British dental journal.
[5] H. Critchley,et al. Connecting brain and body: Transdiagnostic relevance of connective tissue variants to neuropsychiatric symptom expression , 2021, World journal of psychiatry.
[6] P. Byers,et al. The Ehlers–Danlos syndromes , 2020, Nature Reviews Disease Primers.
[7] G. Calcagnini,et al. A new insight on postural tachycardia syndrome in 102 adults with hypermobile Ehlers-Danlos Syndrome/hypermobility spectrum disorder. , 2020, Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace.
[8] M. Ritelli,et al. Molecular Genetics and Pathogenesis of Ehlers–Danlos Syndrome and Related Connective Tissue Disorders , 2020, Genes.
[9] L. Au,et al. Brittle cornea syndrome: current perspectives , 2019, Clinical ophthalmology.
[10] J. Hoffman,et al. Urogenital and pelvic complications in the Ehlers‐Danlos syndromes and associated hypermobility spectrum disorders: A scoping review , 2019, Clinical genetics.
[11] M. Ritelli,et al. Cellular and Molecular Mechanisms in the Pathogenesis of Classical, Vascular, and Hypermobile Ehlers‒Danlos Syndromes , 2019, Genes.
[12] L. Opitz,et al. Transcriptome Profiling of Primary Skin Fibroblasts Reveal Distinct Molecular Features Between PLOD1- and FKBP14-Kyphoscoliotic Ehlers–Danlos Syndrome , 2019, Genes.
[13] E. Henske,et al. The Genetics of Pneumothorax. , 2019, American journal of respiratory and critical care medicine.
[14] D. Milewicz,et al. Spontaneous pneumothorax and hemothorax frequently precede the arterial and intestinal complications of vascular Ehlers–Danlos syndrome , 2019, American journal of medical genetics. Part A.
[15] M. Castori,et al. Clinical Relevance of Joint Hypermobility and Its Impact on Musculoskeletal Pain and Bone Mass , 2018, Current Osteoporosis Reports.
[16] J. Parisi,et al. Bi-allelic Alterations in AEBP1 Lead to Defective Collagen Assembly and Connective Tissue Structure Resulting in a Variant of Ehlers-Danlos Syndrome. , 2018, American journal of human genetics.
[17] Jinxiang Han,et al. Osteogenesis imperfecta type III/Ehlers-Danlos overlap syndrome in a Chinese man. , 2018, Intractable & rare diseases research.
[18] F. Malfait,et al. Vascular phenotypes in nonvascular subtypes of the Ehlers-Danlos syndrome: a systematic review , 2017, Genetics in Medicine.
[19] Stephen H. Bell,et al. A ?scoping review. , 2018, Sexual health.
[20] Ulrich Seidel,et al. Biallelic COL3A1 mutations result in a clinical spectrum of specific structural brain anomalies and connective tissue abnormalities , 2017, American journal of medical genetics. Part A.
[21] J. Belmont,et al. The 2017 international classification of the Ehlers–Danlos syndromes , 2017, American journal of medical genetics. Part C, Seminars in medical genetics.
[22] A. Hakim,et al. Cardiovascular autonomic dysfunction in Ehlers–Danlos syndrome—Hypermobile type , 2017, American journal of medical genetics. Part C, Seminars in medical genetics.
[23] P. Byers,et al. Diagnosis, natural history, and management in vascular Ehlers–Danlos syndrome , 2017, American journal of medical genetics. Part C, Seminars in medical genetics.
[24] R. Engelbert,et al. Disability in Adolescents and Adults Diagnosed With Hypermobility-Related Disorders: A Meta-Analysis. , 2016, Archives of physical medicine and rehabilitation.
[25] R. Baron,et al. Central sensitization as the mechanism underlying pain in joint hypermobility syndrome/Ehlers–Danlos syndrome, hypermobility type , 2016, European journal of pain.
[26] G. Lauria,et al. Small fiber neuropathy is a common feature of Ehlers-Danlos syndromes , 2016, Neurology.
[27] B. Marinelli,et al. Bone involvement in adult patients affected with Ehlers-Danlos syndrome. , 2016, Osteoporosis International.
[28] Blair H. Smith,et al. A classification of chronic pain for ICD-11 , 2015, Pain.
[29] É. Mousseaux,et al. The type of variants at the COL3A1 gene associates with the phenotype and severity of vascular Ehlers–Danlos syndrome , 2015, European Journal of Human Genetics.
[30] P. McCrea,et al. Nuclear signaling from cadherin adhesion complexes. , 2015, Current topics in developmental biology.
[31] J. Van Oosterwijck,et al. Evidence for central sensitization in patients with osteoarthritis pain: A systematic literature review , 2014, European journal of pain.
[32] H. Yoshioka,et al. Sp7/Osterix induces the mouse pro-α2(I) collagen gene (Col1a2) expression via the proximal promoter in osteoblastic cells. , 2014, Biochemical and biophysical research communications.
[33] T. D. de Backer,et al. Dysautonomia and its underlying mechanisms in the hypermobility type of Ehlers-Danlos syndrome. , 2014, Seminars in arthritis and rheumatism.
[34] D. Milewicz,et al. Molecular diagnosis in vascular Ehlers-Danlos syndrome predicts pattern of arterial involvement and outcomes. , 2014, Journal of vascular surgery.
[35] R. Engelbert,et al. Chronic pain in patients with the hypermobility type of Ehlers–Danlos syndrome: evidence for generalized hyperalgesia , 2015, Clinical Rheumatology.
[36] K. Hankenson,et al. Type III Collagen Regulates Osteoblastogenesis and the Quantity of Trabecular Bone , 2014, Calcified Tissue International.
[37] K. Mannerkorpi,et al. Profile of Cerebrospinal microRNAs in Fibromyalgia , 2013, PloS one.
[38] Andy H. Choi,et al. Current Perspectives , 2013, Journal of dental research.
[39] Giorgio Cruccu,et al. Reappraising neuropathic pain in humans—how symptoms help disclose mechanisms , 2013, Nature Reviews Neurology.
[40] J. Clayton-Smith,et al. Brittle cornea syndrome: recognition, molecular diagnosis and management , 2013, Orphanet Journal of Rare Diseases.
[41] D. Eyre,et al. Bone Collagen: New Clues to Its Mineralization Mechanism from Recessive Osteogenesis Imperfecta , 2013, Calcified Tissue International.
[42] H. Kuniyasu,et al. Respiratory complications of Ehlers-Danlos syndrome type IV. , 2013, Legal medicine.
[43] E. Mohammadi,et al. Barriers and facilitators related to the implementation of a physiological track and trigger system: A systematic review of the qualitative evidence , 2017, International journal for quality in health care : journal of the International Society for Quality in Health Care.
[44] W. Frishman,et al. Vascular Ehlers-Danlos Syndrome: Pathophysiology, Diagnosis, and Prevention and Treatment of Its Complications , 2012, Cardiology in review.
[45] M. Baumgartner,et al. Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation , 2011, Orphanet journal of rare diseases.
[46] H. Knoop,et al. Both pain and fatigue are important possible determinants of disability in patients with the Ehlers-Danlos syndrome hypermobility type , 2011, Disability and rehabilitation.
[47] D. Moher,et al. Nonalcoholic Fatty Liver Disease and Acute Ischemic Stroke , 2010 .
[48] A. Farmer,et al. Unexplained gastrointestinal symptoms and joint hypermobility: is connective tissue the missing link? , 2010, Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society.
[49] D. Moher,et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. , 2010, International journal of surgery.
[50] D. Moher,et al. Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement , 2009, BMJ : British Medical Journal.
[51] F. Schmidt. Meta-Analysis , 2008 .
[52] Teresa Foo,et al. : SYSTEMATIC LITERATURE REVIEW , 2004 .
[53] H. Calkins,et al. Orthostatic intolerance and chronic fatigue syndrome associated with Ehlers-Danlos syndrome. , 1999, The Journal of pediatrics.
[54] S R Pinnell,et al. Isolation of type III collagen from human adult parenchymal lung tissue. , 1977, Biochemistry.
[55] M. Das,et al. Ehlers-Danlos Syndrome , 2022, Neurocutaneous Disorders.