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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1967 1
1968 1
1969 1
1970 1
1971 1
1972 2
1973 3
1975 1
1977 1
1978 1
1979 2
1980 4
1982 2
1984 1
1985 1
1986 2
1987 1
1988 1
1990 1
1991 3
1993 4
1994 1
1995 2
1996 3
1997 5
1998 2
1999 5
2000 6
2001 5
2002 6
2003 5
2004 9
2005 4
2006 10
2007 4
2008 7
2009 8
2010 6
2011 9
2012 14
2013 10
2014 17
2015 4
2016 17
2017 8
2018 17
2019 24
2020 23
2021 21
2022 13
2023 15
2024 8

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286 results

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Page 1
Physical therapy treatment of hypermobile Ehlers-Danlos syndrome: A systematic review.
Reychler G, De Backer MM, Piraux E, Poncin W, Caty G. Reychler G, et al. Am J Med Genet A. 2021 Oct;185(10):2986-2994. doi: 10.1002/ajmg.a.62393. Epub 2021 Jun 19. Am J Med Genet A. 2021. PMID: 34145717
Physiotherapy techniques are regularly prescribed in the hypermobile type Ehlers-Danlos syndrome (hEDS) and they are appreciated by the patients. ...Physiotherapy benefits on proprioception and pain in patients with hEDS even if robust randomized contr …
Physiotherapy techniques are regularly prescribed in the hypermobile type Ehlers-Danlos syndrome (hEDS) and they are ap …
The evidence-based rationale for physical therapy treatment of children, adolescents, and adults diagnosed with joint hypermobility syndrome/hypermobile Ehlers Danlos syndrome.
Engelbert RH, Juul-Kristensen B, Pacey V, de Wandele I, Smeenk S, Woinarosky N, Sabo S, Scheper MC, Russek L, Simmonds JV. Engelbert RH, et al. Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):158-167. doi: 10.1002/ajmg.c.31545. Am J Med Genet C Semin Med Genet. 2017. PMID: 28306230 Free article.
New insights into the phenotype of Joint Hypermobility Syndrome (JHS) and Ehlers-Danlos Syndrome-hypermobile type (hEDS) have raised many issues in relation to classification, diagnosis, assessment, and treatment. ...The current evidence-based literature rega …
New insights into the phenotype of Joint Hypermobility Syndrome (JHS) and Ehlers-Danlos Syndrome-hypermobile type (hEDS …
A novel therapeutic strategy for Ehlers-Danlos syndrome based on nutritional supplements.
Mantle D, Wilkins RM, Preedy V. Mantle D, et al. Med Hypotheses. 2005;64(2):279-83. doi: 10.1016/j.mehy.2004.07.023. Med Hypotheses. 2005. PMID: 15607555
Ehlers-Danlos syndrome is a rare disorder, comprising a group of related inherited disorders of connective tissue, resulting from underlying abnormalities in the synthesis and metabolism of collagen. This proposal is specifically concerned with Ehlers- …
Ehlers-Danlos syndrome is a rare disorder, comprising a group of related inherited disorders of connective tissue, resu …
Pathophysiology of Eosinophilic Esophagitis.
O'Shea KM, Aceves SS, Dellon ES, Gupta SK, Spergel JM, Furuta GT, Rothenberg ME. O'Shea KM, et al. Gastroenterology. 2018 Jan;154(2):333-345. doi: 10.1053/j.gastro.2017.06.065. Epub 2017 Jul 27. Gastroenterology. 2018. PMID: 28757265 Free PMC article. Review.
Ehlers-Danlos Syndrome: An Analysis of the Current Treatment Options.
Song B, Yeh P, Nguyen D, Ikpeama U, Epstein M, Harrell J. Song B, et al. Pain Physician. 2020 Jul;23(4):429-438. Pain Physician. 2020. PMID: 32709178 Free article.
BACKGROUND: Ehlers-Danlos syndrome (EDS) is a multifaceted disease that can present with a variety of types of pain. ...Further research and investigation are necessary to develop a comprehensive treatment database for this complex condition. KEY WORDS: Eh …
BACKGROUND: Ehlers-Danlos syndrome (EDS) is a multifaceted disease that can present with a variety of types of pain. .. …
The Ehlers-Danlos syndrome.
Malfait F, De Paepe A. Malfait F, et al. Adv Exp Med Biol. 2014;802:129-43. doi: 10.1007/978-94-007-7893-1_9. Adv Exp Med Biol. 2014. PMID: 24443025 Review.
The Ehlers-Danlos Syndromes comprise a heterogeneous group of diseases, which are characterized by fragility of the soft connective tissues and widespread manifestations in skin, ligaments and joints, blood vessels and internal organs. The clinical spectrum varies from mil …
The Ehlers-Danlos Syndromes comprise a heterogeneous group of diseases, which are characterized by fragility of the soft connective tissues …
Nonatherosclerotic Abdominal Vasculopathies.
Skeik N, Hyde JR, Olson SL, Thaler CM, Abuatiyeh W, Ahmed AK, Lyon DR, Witt DR, Garberich R, Sullivan T. Skeik N, et al. Ann Vasc Surg. 2019 Oct;60:128-146. doi: 10.1016/j.avsg.2019.04.004. Epub 2019 Jun 12. Ann Vasc Surg. 2019. PMID: 31200053
BACKGROUND: Nonatherosclerotic abdominal arterial vasculopathies (NAVs), including mesenteric or renal artery dissection, aneurysm, stenosis, and vasculitis, are rare but have great clinical significance. Patients may present emergently with life-threatening complications …
BACKGROUND: Nonatherosclerotic abdominal arterial vasculopathies (NAVs), including mesenteric or renal artery dissection, aneurysm, stenosis …
Loeys-Dietz syndrome.
Van Laer L, Dietz H, Loeys B. Van Laer L, et al. Adv Exp Med Biol. 2014;802:95-105. doi: 10.1007/978-94-007-7893-1_7. Adv Exp Med Biol. 2014. PMID: 24443023 Review.
Loeys-Dietz syndrome is an autosomal dominant aortic aneurysm syndrome characterized by multisystemic involvement. The most typical clinical triad includes hypertelorism, bifid uvula or cleft palate and aortic aneurysm with tortuosity. ...
Loeys-Dietz syndrome is an autosomal dominant aortic aneurysm syndrome characterized by multisystemic involvement. The most typical clini …
Arterial complications of vascular Ehlers-Danlos syndrome.
Eagleton MJ. Eagleton MJ. J Vasc Surg. 2016 Dec;64(6):1869-1880. doi: 10.1016/j.jvs.2016.06.120. Epub 2016 Sep 26. J Vasc Surg. 2016. PMID: 27687326 Free article. Review.
BACKGROUND: Vascular Ehlers-Danlos syndrome (EDS) is a relatively rare genetic syndrome that occurs owing to disorders in the metabolism of fibrillary collagen. ...
BACKGROUND: Vascular Ehlers-Danlos syndrome (EDS) is a relatively rare genetic syndrome that occurs owing to disorders …
Vascular Ehlers-Danlos Syndrome: Long-Term Observational Study.
Frank M, Adham S, Seigle S, Legrand A, Mirault T, Henneton P, Albuisson J, Denarié N, Mazzella JM, Mousseaux E, Messas E, Boutouyrie P, Jeunemaitre X. Frank M, et al. J Am Coll Cardiol. 2019 Apr 23;73(15):1948-1957. doi: 10.1016/j.jacc.2019.01.058. J Am Coll Cardiol. 2019. PMID: 30999998 Free article.
BACKGROUND: Vascular Ehlers-Danlos syndrome (vEDS) is a rare genetic connective tissue disorder secondary to pathogenic variants within the COL3A1 gene, resulting in exceptional arterial and organ fragility and premature death. The only published clinical …
BACKGROUND: Vascular Ehlers-Danlos syndrome (vEDS) is a rare genetic connective tissue disorder secondary to pathogenic …
286 results