112 related articles for article (PubMed ID: 7795546)
1. [Type VII C Ehlers-Danlos disease or human dermatosparaxia: the product of a fruitful union of so-called fundamental sciences with human and veterinary clinical medicine].
Lapière CM; Nusgens BV
Bull Mem Acad R Med Belg; 1994; 149(5-7):228-34; discussion 235-6. PubMed ID: 7795546
[TBL] [Abstract][Full Text] [Related]
2. Evidence for a relationship between Ehlers-Danlos type VII C in humans and bovine dermatosparaxis.
Nusgens BV; Verellen-Dumoulin C; Hermanns-Lê T; De Paepe A; Nuytinck L; Piérard GE; Lapière CM
Nat Genet; 1992 Jun; 1(3):214-7. PubMed ID: 1303238
[TBL] [Abstract][Full Text] [Related]
3. Further evidence that the failure to cleave the aminopropeptide of type I procollagen is the cause of Ehlers-Danlos syndrome type VII.
Ho KK; Kong RY; Kuffner T; Hsu LH; Ma L; Cheah KS
Hum Mutat; 1994; 3(4):358-64. PubMed ID: 8081389
[TBL] [Abstract][Full Text] [Related]
4. [Hereditary deficiency in the enzymes of the biosynthesis of collagen. The Ehlers-Danlos syndromes (author's transl)].
Gajdos A
Nouv Presse Med; 1977 Oct; 6(34):3101-5. PubMed ID: 21384
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. Heritable collagen disorders: the paradigm of the Ehlers-Danlos syndrome.
Byers PH; Murray ML
J Invest Dermatol; 2012 Nov; 132(E1):E6-11. PubMed ID: 23154631
[No Abstract] [Full Text] [Related]
7. Unusual familial manifestation of Ehlers-Danlos syndrome.
Matton MT; De Paepe A; De Keyser F; François B
Prog Clin Biol Res; 1982; 104():243-58. PubMed ID: 7163270
[TBL] [Abstract][Full Text] [Related]
8. [Ehlers-Danlos syndrome type I. Ultrastructural study].
Paradisi M; Giubilei L; Canzona F; Angelo C; Onetti Muda A; Puddu P
Minerva Pediatr; 1997 May; 49(5):215-9. PubMed ID: 9340484
[TBL] [Abstract][Full Text] [Related]
9. The Ehlers-Danlos syndromes.
Yeowell HN; Pinnell SR
Semin Dermatol; 1993 Sep; 12(3):229-40. PubMed ID: 8217561
[TBL] [Abstract][Full Text] [Related]
10. Heritable diseases of connective tissue.
Krane SM
Monogr Pathol; 1983; 24():31-9. PubMed ID: 6888403
[No Abstract] [Full Text] [Related]
11. Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene.
Colige A; Sieron AL; Li SW; Schwarze U; Petty E; Wertelecki W; Wilcox W; Krakow D; Cohn DH; Reardon W; Byers PH; Lapière CM; Prockop DJ; Nusgens BV
Am J Hum Genet; 1999 Aug; 65(2):308-17. PubMed ID: 10417273
[TBL] [Abstract][Full Text] [Related]
12. Mutations in the lysyl hydroxylase 1 gene that result in enzyme deficiency and the clinical phenotype of Ehlers-Danlos syndrome type VI.
Yeowell HN; Walker LC
Mol Genet Metab; 2000; 71(1-2):212-24. PubMed ID: 11001813
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. [Type I Ehlers-Danlos syndrome].
Lacour JP
Ann Dermatol Venereol; 1998 Dec; 125(12):926. PubMed ID: 9922873
[No Abstract] [Full Text] [Related]
15. [The biochemistry of collagen and the locomotor apparatus. Hereditary diseases of connective tissue and rheumatologic diseases (part 2)].
Peyron JG
Rev Rhum Mal Osteoartic; 1977 Feb; 44(2):135-9. PubMed ID: 300490
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [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]
18. 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]
19. Novel human pathological mutations. Gene symbol: PLOD1. Disease: Ehlers-Danlos syndrome type VIA, kyphoscoliotic type.
Giunta C; Bürer-Chambaz C; Steinmann B
Hum Genet; 2009 Apr; 125(3):346. PubMed ID: 19320026
[No Abstract] [Full Text] [Related]
20. Ehlers-Danlos syndrome: yet another type?
Viljoen D; Goldblatt J; Thompson D; Beighton P
Clin Genet; 1987 Sep; 32(3):196-201. PubMed ID: 3621666
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]