722 related articles for article (PubMed ID: 9557891)
1. Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK).
Beighton P; De Paepe A; Steinmann B; Tsipouras P; Wenstrup RJ
Am J Med Genet; 1998 Apr; 77(1):31-7. PubMed ID: 9557891
[TBL] [Abstract][Full Text] [Related]
2. Ehlers-Danlos syndrome--a historical review.
Parapia LA; Jackson C
Br J Haematol; 2008 Apr; 141(1):32-5. PubMed ID: 18324963
[TBL] [Abstract][Full Text] [Related]
3. [Up-to-date classification and multidisciplinary symptoms of Ehlers-Danlos syndromes].
Ralovich FV; Kiss N; Horváth K; Kárpáti S; Medvecz M
Orv Hetil; 2019 Apr; 160(16):603-612. PubMed ID: 30983397
[TBL] [Abstract][Full Text] [Related]
4. Updates in Clinical and Genetics Aspects of Hypermobile Ehlers Danlos Syndrome.
Forghani I
Balkan Med J; 2019 Jan; 36(1):12-16. PubMed ID: 30063214
[TBL] [Abstract][Full Text] [Related]
5. The Ehlers-Danlos syndromes, rare types.
Brady AF; Demirdas S; Fournel-Gigleux S; Ghali N; Giunta C; Kapferer-Seebacher I; Kosho T; Mendoza-Londono R; Pope MF; Rohrbach M; Van Damme T; Vandersteen A; van Mourik C; Voermans N; Zschocke J; Malfait F
Am J Med Genet C Semin Med Genet; 2017 Mar; 175(1):70-115. PubMed ID: 28306225
[TBL] [Abstract][Full Text] [Related]
6. The 2017 international classification of the Ehlers-Danlos syndromes.
Malfait F; Francomano C; Byers P; Belmont J; Berglund B; Black J; Bloom L; Bowen JM; Brady AF; Burrows NP; Castori M; Cohen H; Colombi M; Demirdas S; De Backer J; De Paepe A; Fournel-Gigleux S; Frank M; Ghali N; Giunta C; Grahame R; Hakim A; Jeunemaitre X; Johnson D; Juul-Kristensen B; Kapferer-Seebacher I; Kazkaz H; Kosho T; Lavallee ME; Levy H; Mendoza-Londono R; Pepin M; Pope FM; Reinstein E; Robert L; Rohrbach M; Sanders L; Sobey GJ; Van Damme T; Vandersteen A; van Mourik C; Voermans N; Wheeldon N; Zschocke J; Tinkle B
Am J Med Genet C Semin Med Genet; 2017 Mar; 175(1):8-26. PubMed ID: 28306229
[TBL] [Abstract][Full Text] [Related]
7. [Ehlers-Danlos syndrome--diagnosis and subclassification].
Rand-Hendriksen S; Wekre LL; Paus B
Tidsskr Nor Laegeforen; 2006 Aug; 126(15):1903-7. PubMed ID: 16915311
[TBL] [Abstract][Full Text] [Related]
8. Application of the 2017 criteria for vascular Ehlers-Danlos syndrome in 50 patients ascertained according to the Villefranche nosology.
Ritelli M; Rovati C; Venturini M; Chiarelli N; Cinquina V; Castori M; Colombi M
Clin Genet; 2020 Feb; 97(2):287-295. PubMed ID: 31600821
[TBL] [Abstract][Full Text] [Related]
9. Accuracy of Clinical Diagnostic Criteria for Patients With Vascular Ehlers-Danlos Syndrome in a Tertiary Referral Centre.
Henneton P; Albuisson J; Adham S; Legrand A; Mazzella JM; Jeunemaitre X; Frank M
Circ Genom Precis Med; 2019 Mar; 12(3):e001996. PubMed ID: 30919682
[TBL] [Abstract][Full Text] [Related]
10. [Ehlers-Danlos syndromes].
Germain DP
Ann Dermatol Venereol; 2017 Dec; 144(12):744-758. PubMed ID: 29032848
[TBL] [Abstract][Full Text] [Related]
11. Ehlers-Danlos syndrome: classifications, oral manifestations, and dental considerations.
Abel MD; Carrasco LR
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2006 Nov; 102(5):582-90. PubMed ID: 17052632
[TBL] [Abstract][Full Text] [Related]
12. Spectrum of mucocutaneous, ocular and facial features and delineation of novel presentations in 62 classical Ehlers-Danlos syndrome patients.
Colombi M; Dordoni C; Venturini M; Ciaccio C; Morlino S; Chiarelli N; Zanca A; Calzavara-Pinton P; Zoppi N; Castori M; Ritelli M
Clin Genet; 2017 Dec; 92(6):624-631. PubMed ID: 28485813
[TBL] [Abstract][Full Text] [Related]
13. Ehlers-Danlos syndrome.
Grahame R
S Afr Med J; 2016 May; 106(6 Suppl 1):S45-6. PubMed ID: 27245524
[TBL] [Abstract][Full Text] [Related]
14. Ehlers-Danlos syndrome, classical type.
Bowen JM; Sobey GJ; Burrows NP; Colombi M; Lavallee ME; Malfait F; Francomano CA
Am J Med Genet C Semin Med Genet; 2017 Mar; 175(1):27-39. PubMed ID: 28192633
[TBL] [Abstract][Full Text] [Related]
15. The international consortium on the Ehlers-Danlos syndromes.
Bloom L; Byers P; Francomano C; Tinkle B; Malfait F;
Am J Med Genet C Semin Med Genet; 2017 Mar; 175(1):5-7. PubMed ID: 28306227
[TBL] [Abstract][Full Text] [Related]
16. Hypermobile Ehlers-Danlos syndrome: A review and a critical appraisal of published genetic research to date.
Scicluna K; Formosa MM; Farrugia R; Borg I
Clin Genet; 2022 Jan; 101(1):20-31. PubMed ID: 34219226
[TBL] [Abstract][Full Text] [Related]
17. Well-defined clinical presentation of Ehlers-Danlos syndrome in patients with tenascin-X deficiency: a report of four cases.
Hendriks AGM; Voermans NC; Schalkwijk J; Hamel BC; van Rossum MM
Clin Dysmorphol; 2012 Jan; 21(1):15-18. PubMed ID: 21959861
[TBL] [Abstract][Full Text] [Related]
18. [Joint hypermobility, skin hyper-elasticity, connective tissue fragility: classical symptoms of Ehlers-Danlos syndrome].
Häggblom L; Sanner G
Lakartidningen; 1995 Dec; 92(50):4809-13. PubMed ID: 8538298
[No Abstract] [Full Text] [Related]
19. An acquired or heritable connective tissue disorder? A review of hypermobile Ehlers Danlos Syndrome.
Martin A
Eur J Med Genet; 2019 Jul; 62(7):103672. PubMed ID: 31102747
[TBL] [Abstract][Full Text] [Related]
20. A framework for the classification of joint hypermobility and related conditions.
Castori M; Tinkle B; Levy H; Grahame R; Malfait F; Hakim A
Am J Med Genet C Semin Med Genet; 2017 Mar; 175(1):148-157. PubMed ID: 28145606
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
