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Year Number of Results
1936 1
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1948 8
1949 7
1950 11
1951 9
1952 19
1953 12
1954 13
1955 13
1956 16
1957 5
1958 6
1959 15
1960 10
1961 9
1962 12
1963 27
1964 26
1965 26
1966 24
1967 29
1968 26
1969 51
1970 32
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1972 38
1973 33
1974 28
1975 42
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1983 29
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1988 54
1989 66
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1992 45
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2002 56
2003 47
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2005 94
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2008 96
2009 93
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2011 141
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4,787 results
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Page 1
The Many Facets of Hypermobile Ehlers-Danlos Syndrome.
Riley B. Riley B. J Am Osteopath Assoc. 2020 Jan 1;120(1):30-32. doi: 10.7556/jaoa.2020.012. J Am Osteopath Assoc. 2020. PMID: 31904772 Free article. Review.
Of the 13 subtypes of Ehlers-Danlos Syndromes (EDSs) identified in the 2017 international classification of EDSs, 12 have a recognized, associated genetic mutation. ...
Of the 13 subtypes of Ehlers-Danlos Syndromes (EDSs) identified in the 2017 international classification of EDSs, 12 have a re …
[Ehlers-Danlos syndrome].
Leganger J, Søborg ML, Farholt S, Lund AM, Rosenberg J, Burcharth J. Leganger J, et al. Ugeskr Laeger. 2016 Apr 25;178(17):V01160014. Ugeskr Laeger. 2016. PMID: 27136954 Free article. Review. Danish.
Ehlers-Danlos syndrome (EDS) comprises a group of diseases characterized by connective tissue fragility. ...
Ehlers-Danlos syndrome (EDS) comprises a group of diseases characterized by connective tissue fragility. ...
Ehlers-Danlos syndrome.
Grahame R. Grahame R. S Afr Med J. 2016 May 25;106(6 Suppl 1):S45-6. doi: 10.7196/SAMJ.2016.v106i6.10991. S Afr Med J. 2016. PMID: 27245524
The Ehlers-Danlos syndromes (EDSs) were originally described by Ehlers in Denmark and Danlos in Paris in 1898 and 1908, respectively. ...
The Ehlers-Danlos syndromes (EDSs) were originally described by Ehlers in Denmark and Danlos in Paris in 1898 an …
Hypermobile Ehlers-Danlos syndrome (a.k.a. Ehlers-Danlos syndrome Type III and Ehlers-Danlos syndrome hypermobility type): Clinical description and natural history.
Tinkle B, Castori M, Berglund B, Cohen H, Grahame R, Kazkaz H, Levy H. Tinkle B, et al. Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):48-69. doi: 10.1002/ajmg.c.31538. Epub 2017 Feb 1. Am J Med Genet C Semin Med Genet. 2017. PMID: 28145611 Review.
The hypermobile type of Ehlers-Danlos syndrome (hEDS) is likely the most common hereditary disorder of connective tissue. ...Two undifferentiated syndromes have been used to describe these manifestations-joint hypermobility syndrome and hEDS. Both are …
The hypermobile type of Ehlers-Danlos syndrome (hEDS) is likely the most common hereditary disorder of connective tissu …
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. ...
New insights into the phenotype of Joint Hypermobility Syndrome (JHS) and Ehlers-Danlos Syndrome-hypermobile typ …
Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type.
Malfait F, Wenstrup RJ, De Paepe A. Malfait F, et al. Genet Med. 2010 Oct;12(10):597-605. doi: 10.1097/GIM.0b013e3181eed412. Genet Med. 2010. PMID: 20847697 Free article. Review.
It comprises Ehlers-Danlos syndrome type I and Ehlers-Danlos syndrome type II, but it is now apparent that these form a continuum of clinical findings and differ only in phenotypic severity. ...No treatment for the underlying defect is pr …
It comprises Ehlers-Danlos syndrome type I and Ehlers-Danlos syndrome type II, but it is now appar …
Ehlers-Danlos syndrome--a historical review.
Parapia LA, Jackson C. Parapia LA, et al. Br J Haematol. 2008 Apr;141(1):32-5. doi: 10.1111/j.1365-2141.2008.06994.x. Br J Haematol. 2008. PMID: 18324963 Free article.
Ehlers-Danlos syndrome is an inherited heterogeneous group of connective tissue disorders, characterized by abnormal collagen synthesis, affecting skin, ligaments, joints, blood vessels and other organs. ...In 1998, Beighton published the classification of …
Ehlers-Danlos syndrome is an inherited heterogeneous group of connective tissue disorders, characterized by abnormal co …
Diagnosis, natural history, and management in vascular Ehlers-Danlos syndrome.
Byers PH, Belmont J, Black J, De Backer J, Frank M, Jeunemaitre X, Johnson D, Pepin M, Robert L, Sanders L, Wheeldon N. Byers PH, et al. Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):40-47. doi: 10.1002/ajmg.c.31553. Am J Med Genet C Semin Med Genet. 2017. PMID: 28306228 Review.
Vascular Ehlers Danlos syndrome (vEDS) is an uncommon genetic disorders characterized by arterial aneurysm, dissection and rupture, bowel rupture, and rupture of the gravid uterus. ...
Vascular Ehlers Danlos syndrome (vEDS) is an uncommon genetic disorders characterized by arterial aneurysm, dissection …
Ehlers-Danlos Syndrome Type Arthrochalasia: A Systematic Review.
Martín-Martín M, Cortés-Martín J, Tovar-Gálvez MI, Sánchez-García JC, Díaz-Rodríguez L, Rodríguez-Blanque R. Martín-Martín M, et al. Int J Environ Res Public Health. 2022 Feb 7;19(3):1870. doi: 10.3390/ijerph19031870. Int J Environ Res Public Health. 2022. PMID: 35162892 Free PMC article. Review.
Ehlers-Danlos syndrome type arthrochalasia (aEDS) is a rare genetic disease characterized by severe generalized joint hypermobility, bilateral congenital hip dislocation, skin hyperextensibility, muscle hypotonia, and mild dysmorphic features. ...The main obj …
Ehlers-Danlos syndrome type arthrochalasia (aEDS) is a rare genetic disease characterized by severe generalized joint h …
Molecular Genetics and Pathogenesis of Ehlers-Danlos Syndrome and Related Connective Tissue Disorders.
Ritelli M, Colombi M. Ritelli M, et al. Genes (Basel). 2020 May 13;11(5):547. doi: 10.3390/genes11050547. Genes (Basel). 2020. PMID: 32414079 Free PMC article.
Ehlers-Danlos syndromes (EDS) are a group of heritable connective tissue disorders (HCTDs) characterized by a variable degree of skin hyperextensibility, joint hypermobility and tissue fragility. ...EDS need to be differentiated from other HCTDs with a variable clin …
Ehlers-Danlos syndromes (EDS) are a group of heritable connective tissue disorders (HCTDs) characterized by a variable degree …
4,787 results

Searches related to "ehlers-danlos syndrome"