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.
330 related articles for article (PubMed ID: 27582382)
1. 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]
2. Measurement of serum tenascin-X in patients with congenital adrenal hyperplasia at risk for Ehlers-Danlos contiguous gene deletion syndrome CAH-X. Kolli V; Kim H; Rao H; Lao Q; Gaynor A; Milner JD; Merke DP BMC Res Notes; 2019 Oct; 12(1):711. PubMed ID: 31666125 [TBL] [Abstract][Full Text] [Related]
3. Elastic fiber abnormalities in hypermobility type Ehlers-Danlos syndrome patients with tenascin-X mutations. Zweers MC; Dean WB; van Kuppevelt TH; Bristow J; Schalkwijk J Clin Genet; 2005 Apr; 67(4):330-4. PubMed ID: 15733269 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. A TNXB splice donor site variant as a cause of hypermobility type Ehlers-Danlos syndrome in patients with congenital adrenal hyperplasia. Lao Q; Mallappa A; Rueda Faucz F; Joyal E; Veeraraghavan P; Chen W; Merke DP Mol Genet Genomic Med; 2021 Feb; 9(2):e1556. PubMed ID: 33332743 [TBL] [Abstract][Full Text] [Related]
6. Tenascin-X haploinsufficiency associated with Ehlers-Danlos syndrome in patients with congenital adrenal hyperplasia. Merke DP; Chen W; Morissette R; Xu Z; Van Ryzin C; Sachdev V; Hannoush H; Shanbhag SM; Acevedo AT; Nishitani M; Arai AE; McDonnell NB J Clin Endocrinol Metab; 2013 Feb; 98(2):E379-87. PubMed ID: 23284009 [TBL] [Abstract][Full Text] [Related]
8. Rare neurological manifestations in a Saudi Arabian patient with Ehlers-Danlos syndrome and a novel homozygous variant in the TNXB gene. Al-Harbi TM; Al-Rammah H; Al-Zahrani N; Liu Y; Sleiman PMA; Dridi W; Hakonarson H Am J Med Genet A; 2022 Feb; 188(2):618-623. PubMed ID: 34636138 [TBL] [Abstract][Full Text] [Related]
9. A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency. Schalkwijk J; Zweers MC; Steijlen PM; Dean WB; Taylor G; van Vlijmen IM; van Haren B; Miller WL; Bristow J N Engl J Med; 2001 Oct; 345(16):1167-75. PubMed ID: 11642233 [TBL] [Abstract][Full Text] [Related]
10. Tenascin-X: a candidate gene for benign joint hypermobility syndrome and hypermobility type Ehlers-Danlos syndrome? Zweers MC; Kucharekova M; Schalkwijk J Ann Rheum Dis; 2005 Mar; 64(3):504-5. PubMed ID: 15708907 [No Abstract] [Full Text] [Related]
12. Clinical and Molecular Characterization of Classical-Like Ehlers-Danlos Syndrome Due to a Novel Rymen D; Ritelli M; Zoppi N; Cinquina V; Giunta C; Rohrbach M; Colombi M Genes (Basel); 2019 Oct; 10(11):. PubMed ID: 31731524 [TBL] [Abstract][Full Text] [Related]
13. The Prevalence of the Chimeric TNXA/TNXB Gene and Clinical Symptoms of Ehlers-Danlos Syndrome with 21-Hydroxylase Deficiency. Gao Y; Lu L; Yu B; Mao J; Wang X; Nie M; Wu X J Clin Endocrinol Metab; 2020 Jul; 105(7):. PubMed ID: 32291442 [TBL] [Abstract][Full Text] [Related]
14. Tenascin-X, Congenital Adrenal Hyperplasia, and the CAH-X Syndrome. Miller WL; Merke DP Horm Res Paediatr; 2018; 89(5):352-361. PubMed ID: 29734195 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Bi-allelic AEBP1 mutations in two patients with Ehlers-Danlos syndrome. Syx D; De Wandele I; Symoens S; De Rycke R; Hougrand O; Voermans N; De Paepe A; Malfait F Hum Mol Genet; 2019 Jun; 28(11):1853-1864. PubMed ID: 30668708 [TBL] [Abstract][Full Text] [Related]