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

Year Number of Results
1936 1
1937 2
1938 2
1939 3
1942 1
1946 9
1947 7
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
1971 32
1972 38
1973 33
1974 28
1975 42
1976 29
1977 37
1978 26
1979 44
1980 45
1981 35
1982 41
1983 29
1984 56
1985 51
1986 41
1987 47
1988 54
1989 66
1990 56
1991 60
1992 45
1993 68
1994 62
1995 56
1996 60
1997 73
1998 59
1999 67
2000 78
2001 75
2002 56
2003 47
2004 75
2005 94
2006 94
2007 74
2008 96
2009 93
2010 96
2011 141
2012 150
2013 162
2014 178
2015 157
2016 157
2017 173
2018 195
2019 257
2020 266
2021 304
2022 300
2023 315
2024 168

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5,145 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 …
Hypermobile Ehlers-Danlos syndrome and disorders of the gastrointestinal tract: What the gastroenterologist needs to know.
Thwaites PA, Gibson PR, Burgell RE. Thwaites PA, et al. J Gastroenterol Hepatol. 2022 Sep;37(9):1693-1709. doi: 10.1111/jgh.15927. Epub 2022 Jul 20. J Gastroenterol Hepatol. 2022. PMID: 35750466 Free PMC article. Review.
BACKGROUND AND AIM: Hypermobile Ehlers-Danlos syndrome (hEDS) and the hypermobility spectrum disorders (HSD) can be challenging to diagnose and manage. ...METHODS: Literature relevant to the gastrointestinal system and hypermobile Ehlers-Danlos
BACKGROUND AND AIM: Hypermobile Ehlers-Danlos syndrome (hEDS) and the hypermobility spectrum disorders (HSD) can be cha …
[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. ...
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 …
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
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
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 …
Neuro-ophthalmic manifestations of Ehlers-Danlos syndrome.
Rachapudi SS, Laylani NA, Davila-Siliezar PA, Lee AG. Rachapudi SS, et al. Curr Opin Ophthalmol. 2023 Nov 1;34(6):476-480. doi: 10.1097/ICU.0000000000001002. Epub 2023 Aug 30. Curr Opin Ophthalmol. 2023. PMID: 37729660 Review.
PURPOSE OF REVIEW: To review the neuro-ophthalmic manifestations of Ehlers-Danlos syndrome (EDS). RECENT FINDINGS: Ehlers-Danlos syndrome (EDS) is a rare genetic disorder with an estimated prevalence of 1 in 5000 individuals, but its true …
PURPOSE OF REVIEW: To review the neuro-ophthalmic manifestations of Ehlers-Danlos syndrome (EDS). RECENT FINDINGS: E
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
Ehlers-Danlos syndrome.
Atkinson G. Atkinson G. Br Dent J. 2020 Aug;229(3):153. doi: 10.1038/s41415-020-2019-3. Br Dent J. 2020. PMID: 32811922 No abstract available.
5,145 results