140 related articles for article (PubMed ID: 3491758)
1. Biochemical, morphological and immunological findings in a patient with a cutis laxa-associated inborn disorder (De Barsy syndrome).
Pontz BF; Zepp F; Stöss H
Eur J Pediatr; 1986 Oct; 145(5):428-34. PubMed ID: 3491758
[TBL] [Abstract][Full Text] [Related]
2. A disease with features of cutis laxa and Ehlers-Danlos syndrome. Report of a mother and daughter.
Tsukahara M; Shinkai H; Asagami C; Eguchi T; Kajii T
Hum Genet; 1988 Jan; 78(1):9-12. PubMed ID: 3338795
[TBL] [Abstract][Full Text] [Related]
3. The De Barsy syndrome.
Guerra D; Fornieri C; Bacchelli B; Lugli L; Torelli P; Balli F; Ferrari P
J Cutan Pathol; 2004 Oct; 31(9):616-24. PubMed ID: 15330994
[TBL] [Abstract][Full Text] [Related]
4. Heterogeneity of elastin expression in cutis laxa fibroblast strains.
Sephel GC; Byers PH; Holbrook KA; Davidson JM
J Invest Dermatol; 1989 Jul; 93(1):147-53. PubMed ID: 2745999
[TBL] [Abstract][Full Text] [Related]
5. Collagen studies in congenital cutis laxa.
Taïeb A; Aumailley M; Courouge-Dorcier D; Rabaud M; Bioulac-Sage P; Surlève-Bazeille JE; Maleville J
Arch Dermatol Res; 1987; 279(5):308-14. PubMed ID: 3632035
[TBL] [Abstract][Full Text] [Related]
6. Cutis laxa, congenital form with pulmonary emphysema: an ultrastructural study.
Ledoux-Corbusier M
J Cutan Pathol; 1983 Oct; 10(5):340-9. PubMed ID: 6630666
[TBL] [Abstract][Full Text] [Related]
7. Increased expression of type VI collagen genes in cutis laxa fibroblasts.
Hatamochi A; Arakawa M; Mori K; Mori Y; Ueki H; Yoshioka H
J Dermatol Sci; 1996 Feb; 11(2):97-103. PubMed ID: 8869029
[TBL] [Abstract][Full Text] [Related]
8. Severe congenital cutis laxa with cardiovascular manifestations due to homozygous deletions in ALDH18A1.
Fischer B; Callewaert B; Schröter P; Coucke PJ; Schlack C; Ott CE; Morroni M; Homann W; Mundlos S; Morava E; Ficcadenti A; Kornak U
Mol Genet Metab; 2014 Aug; 112(4):310-6. PubMed ID: 24913064
[TBL] [Abstract][Full Text] [Related]
9. Cutis laxa. Ultrastructural and biochemical studies.
Hashimoto K; Kanzaki T
Arch Dermatol; 1975 Jul; 111(7):861-73. PubMed ID: 1147631
[TBL] [Abstract][Full Text] [Related]
10. Acquired cutis laxa (generalized elastolysis): light and electron microscopic studies.
Nanko H; Jepsen LV; Zachariae H; Søgaard H
Acta Derm Venereol; 1979; 59(4):315-24. PubMed ID: 92145
[TBL] [Abstract][Full Text] [Related]
11. Cutis Laxa syndrome: a case report.
Hbibi M; Abourazzak S; Idrissi M; Chaouki S; Atmani S; Hida M
Pan Afr Med J; 2015; 20():3. PubMed ID: 25995800
[TBL] [Abstract][Full Text] [Related]
12. Autosomal recessive cutis laxa syndrome. A case report.
Jung K; Ueberham U; Hausser I; Bosler K; John B; Linse R
Acta Derm Venereol; 1996 Jul; 76(4):298-301. PubMed ID: 8869689
[TBL] [Abstract][Full Text] [Related]
13. Bilateral congenital entropion with cutis laxa.
Al-Faky YH; Salih MA; Mubarak M; Al-Rikabi AC
Pediatr Dermatol; 2014; 31(3):e82-4. PubMed ID: 24517732
[TBL] [Abstract][Full Text] [Related]
14. Acquired cutis laxa type II (Marshall syndrome) in an 18-month-old child: a case report.
Haider M; Alfadley A; Kadry R; Almutawa A
Pediatr Dermatol; 2010; 27(1):89-91. PubMed ID: 20199420
[TBL] [Abstract][Full Text] [Related]
15. Morphometric analysis of elastic skin fibres from patients with: cutis laxa, anetoderma, pseudoxanthoma elasticum, and Buschke-Ollendorff and Williams-Beuren syndromes.
Ghomrasseni S; Dridi M; Bonnefoix M; Septier D; Gogly G; Pellat B; Godeau G
J Eur Acad Dermatol Venereol; 2001 Jul; 15(4):305-11. PubMed ID: 11730039
[TBL] [Abstract][Full Text] [Related]
16. [Congenital generalized cutis laxa: 5 cases].
Rybojad M; Baumann C; Godeau G; Moraillon I; Prigent F; Morel P; Bourrat E
Ann Dermatol Venereol; 1999 Apr; 126(4):317-9. PubMed ID: 10421933
[TBL] [Abstract][Full Text] [Related]
17. Ultrastructural demonstration of a relationship between acquired cutis laxa and monoclonal gammopathy.
Maruani A; Arbeille B; Machet MC; Barbet C; Laure B; Martin L; Machet L
Acta Derm Venereol; 2010 Jul; 90(4):406-8. PubMed ID: 20574607
[TBL] [Abstract][Full Text] [Related]
18. De Barsy syndrome: a review of the phenotype.
Kivuva EC; Parker MJ; Cohen MC; Wagner BE; Sobey G
Clin Dysmorphol; 2008 Apr; 17(2):99-107. PubMed ID: 18388779
[TBL] [Abstract][Full Text] [Related]
19. A familial cutis laxa syndrome with ultrastructural abnormalities of collagen and elastin.
Marchase P; Holbrook K; Pinnell SR
J Invest Dermatol; 1980 Nov; 75(5):399-403. PubMed ID: 7430706
[TBL] [Abstract][Full Text] [Related]
20. Collagen metabolism in cutis laxa fibroblasts: increased collagenase gene expression associated with unaltered expression of type I and type III collagen.
Hatamochi A; Wada T; Takeda K; Ueki H; Kawano S; Terada K; Morita T
J Invest Dermatol; 1991 Sep; 97(3):483-7. PubMed ID: 1651970
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]