These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
319 related articles for article (PubMed ID: 28485813)
1. 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]
2. Multisystemic manifestations in a cohort of 75 classical Ehlers-Danlos syndrome patients: natural history and nosological perspectives. Ritelli M; Venturini M; Cinquina V; Chiarelli N; Colombi M Orphanet J Rare Dis; 2020 Jul; 15(1):197. PubMed ID: 32736638 [TBL] [Abstract][Full Text] [Related]
3. Clinical and molecular characterization of 40 patients with classic Ehlers-Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations. Ritelli M; Dordoni C; Venturini M; Chiarelli N; Quinzani S; Traversa M; Zoppi N; Vascellaro A; Wischmeijer A; Manfredini E; Garavelli L; Calzavara-Pinton P; Colombi M Orphanet J Rare Dis; 2013 Apr; 8():58. PubMed ID: 23587214 [TBL] [Abstract][Full Text] [Related]
4. Identification of the novel COL5A1 c.3369_3431dup, p.(Glu1124_Gly1144dup) variant in a patient with incomplete classical Ehlers-Danlos syndrome: The importance of phenotype-guided genetic testing. Ritelli M; Cinquina V; Venturini M; Colombi M Mol Genet Genomic Med; 2020 Oct; 8(10):e1422. PubMed ID: 32720758 [TBL] [Abstract][Full Text] [Related]
5. Spectrum of mucocutaneous manifestations in 277 patients with joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type. Castori M; Dordoni C; Morlino S; Sperduti I; Ritelli M; Valiante M; Chiarelli N; Zanca A; Celletti C; Venturini M; Camerota F; Calzavara-Pinton P; Grammatico P; Colombi M Am J Med Genet C Semin Med Genet; 2015 Mar; 169C(1):43-53. PubMed ID: 25655071 [TBL] [Abstract][Full Text] [Related]
6. Arterial complications in classical Ehlers-Danlos syndrome: a case series. Angwin C; Brady AF; Pope FM; Vandersteen A; Baker D; Cheema H; Sobey G; Johnson D; von Klemperer K; Kazkaz H; van Dijk F; Ghali N J Med Genet; 2020 Nov; 57(11):769-776. PubMed ID: 32467296 [TBL] [Abstract][Full Text] [Related]
7. A classical Ehlers-Danlos syndrome family with incomplete presentation diagnosed by molecular testing. Colombi M; Dordoni C; Cinquina V; Venturini M; Ritelli M Eur J Med Genet; 2018 Jan; 61(1):17-20. PubMed ID: 29024828 [TBL] [Abstract][Full Text] [Related]
9. Molecular insights in the pathogenesis of classical Ehlers-Danlos syndrome from transcriptome-wide expression profiling of patients' skin fibroblasts. Chiarelli N; Carini G; Zoppi N; Ritelli M; Colombi M PLoS One; 2019; 14(2):e0211647. PubMed ID: 30716086 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Evaluation of a patient with classical Ehlers-Danlos syndrome due to a 9q34 duplication affecting COL5A1. Kuroda Y; Ohashi I; Naruto T; Ida K; Enomoto Y; Saito T; Nagai JI; Kurosawa K Congenit Anom (Kyoto); 2018 Nov; 58(6):191-193. PubMed ID: 29520887 [TBL] [Abstract][Full Text] [Related]
12. Homozygosity and Heterozygosity for Null Col5a2 Alleles Produce Embryonic Lethality and a Novel Classic Ehlers-Danlos Syndrome-Related Phenotype. Park AC; Phillips CL; Pfeiffer FM; Roenneburg DA; Kernien JF; Adams SM; Davidson JM; Birk DE; Greenspan DS Am J Pathol; 2015 Jul; 185(7):2000-11. PubMed ID: 25987251 [TBL] [Abstract][Full Text] [Related]
13. A case of Ehlers-Danlos syndrome presenting with widened atrophic scars of forehead, elbow, knee, and pretibial area: A case report. Xu X; Wang Z; Zan T Medicine (Baltimore); 2019 Sep; 98(37):e17138. PubMed ID: 31517854 [TBL] [Abstract][Full Text] [Related]
14. Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type. Malfait F; Wenstrup RJ; De Paepe A Genet Med; 2010 Oct; 12(10):597-605. PubMed ID: 20847697 [TBL] [Abstract][Full Text] [Related]
15. Recognizing the tenascin-X deficient type of Ehlers-Danlos syndrome: a cross-sectional study in 17 patients. Demirdas S; Dulfer E; Robert L; Kempers M; van Beek D; Micha D; van Engelen BG; Hamel B; Schalkwijk J; Loeys B; Maugeri A; Voermans NC Clin Genet; 2017 Mar; 91(3):411-425. PubMed ID: 27582382 [TBL] [Abstract][Full Text] [Related]
16. Clinical and molecular characteristics of 168 probands and 65 relatives with a clinical presentation of classical Ehlers-Danlos syndrome. Colman M; Syx D; De Wandele I; Dhooge T; Symoens S; Malfait F Hum Mutat; 2021 Oct; 42(10):1294-1306. PubMed ID: 34265140 [TBL] [Abstract][Full Text] [Related]
17. Expanding the Clinical and Mutational Spectrum of Recessive Ritelli M; Cinquina V; Venturini M; Pezzaioli L; Formenti AM; Chiarelli N; Colombi M Genes (Basel); 2019 Feb; 10(2):. PubMed ID: 30759870 [TBL] [Abstract][Full Text] [Related]
18. Deficits in Col5a2 Expression Result in Novel Skin and Adipose Abnormalities and Predisposition to Aortic Aneurysms and Dissections. Park AC; Phan N; Massoudi D; Liu Z; Kernien JF; Adams SM; Davidson JM; Birk DE; Liu B; Greenspan DS Am J Pathol; 2017 Oct; 187(10):2300-2311. PubMed ID: 28734943 [TBL] [Abstract][Full Text] [Related]
19. Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria. Symoens S; Syx D; Malfait F; Callewaert B; De Backer J; Vanakker O; Coucke P; De Paepe A Hum Mutat; 2012 Oct; 33(10):1485-93. PubMed ID: 22696272 [TBL] [Abstract][Full Text] [Related]