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Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation In: Orphanet Journal of Rare Diseases. Band 6, 2011, S. 46, ISSN1750-1172. doi:10.1186/1750-1172-2-32. PMID 17640391. PMC 3135503 (freier Volltext). (Review).
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Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation In: Orphanet Journal of Rare Diseases. Band 6, 2011, S. 46, ISSN1750-1172. doi:10.1186/1750-1172-2-32. PMID 17640391. PMC 3135503 (freier Volltext). (Review).
Britta Berglund, Mattiasson Anne-Cathrine, Ingrid Randers: Dignity not fully upheld when seeking health care: experiences expressed by individuals suffering from Ehlers-Danlos syndrome. In: Disability and Rehabilitation. Band32, Nr.1, 2010, ISSN0963-8288, S.1–7, doi:10.3109/09638280903178407, PMID 19925271.
I. Robertson: Keratoconus and the Ehlers-Danlos syndrome: a new aspect of keratoconus. In: The Medical journal of Australia. Band 1, Nummer 18, Mai 1975, S. 571–573, ISSN0025-729X. PMID 1143149.
R. K. MISHRA, I. B. GOEL: DISCIFORM MACULAR DEGENERATION ASSOCIATED WITH EHLERS-DANLOS SYNDROME. (CUTIS HYPERELESTICA). In: Journal of the All-India Ophthalmological Society. Band 11, Dezember 1963, S. 87–95, ISSN0044-7307. PMID 14098999.
N. C. Voermans, H. Knoop u. a.: Pain in ehlers-danlos syndrome is common, severe, and associated with functional impairment. In: Journal of pain and symptom management. Band 40, Nummer 3, September 2010, S. 370–378, ISSN1873-6513. doi:10.1016/j.jpainsymman.2009.12.026. PMID 20579833.
N. C. Voermans, H. Knoop u. a.: Pain in ehlers-danlos syndrome is common, severe, and associated with functional impairment. In: Journal of pain and symptom management. Band 40, Nummer 3, September 2010, S. 370–378, ISSN1873-6513. doi:10.1016/j.jpainsymman.2009.12.026. PMID 20579833.
Pradeep Chopra, Brad Tinkle, Claude Hamonet, Isabelle Brock, Anne Gompel: Pain management in the Ehlers–Danlos syndromes. In: American Journal of Medical Genetics Part C: Seminars in Medical Genetics. Band175, Nr.1, 2017, ISSN1552-4876, S.212–219, doi:10.1002/ajmg.c.31554.
L. Remvig, D. V. Jensen, R. C. Ward: Are diagnostic criteria for general joint hypermobility and benign joint hypermobility syndrome based on reproducible and valid tests? A review of the literature. In: The Journal of Rheumatology. Band 34, 2007, S. 798–803, ISSN0315-162X. PMID 17295436. (Review).
I. Bjelland, G. S. Tell u. a.: Folate, vitamin B12, homocysteine, and the MTHFR 677C->T polymorphism in anxiety and depression: the Hordaland Homocysteine Study. In: Archives of general psychiatry. Band 60, Nummer 6, Juni 2003, S. 618–626, ISSN0003-990X. doi:10.1001/archpsyc.60.6.618. PMID 12796225.
L. Yan, L. Zhao u. a.: Association of the maternal MTHFR C677T polymorphism with susceptibility to neural tube defects in offsprings: evidence from 25 case-control studies. In: PloS one. Band 7, Nummer 10, 2012, S. e41689, ISSN1932-6203. doi:10.1371/journal.pone.0041689. PMID 23056169. PMC 3463537 (freier Volltext).
Z. H. Shagirova, L. N. Ushenkova u. a.: [Investigation of detoxification polymorphisms genes, methylenetetrahydrofolate-reductase (MTHFR) and P53 in the radiosensitive human cells]. In: Radiatsionnaia biologiia, radioecologiia. Band 50, Nummer 2, 2010 Mar-Apr, S. 128–133, ISSN0869-8031. PMID 20464958.