148 related articles for article (PubMed ID: 9111998)
1. Congenital cutis laxa and lysyl oxidase deficiency.
Khakoo A; Thomas R; Trompeter R; Duffy P; Price R; Pope FM
Clin Genet; 1997 Feb; 51(2):109-14. PubMed ID: 9111998
[TBL] [Abstract][Full Text] [Related]
2. X-linked cutis laxa: defective cross-link formation in collagen due to decreased lysyl oxidase activity.
Byers PH; Siegel RC; Holbrook KA; Narayanan AS; Bornstein P; Hall JG
N Engl J Med; 1980 Jul; 303(2):61-5. PubMed ID: 6104292
[TBL] [Abstract][Full Text] [Related]
3. Expression of mRNAs for lysyl oxidase and type III procollagen in cultured fibroblasts from patients with the Menkes and occipital horn syndromes as determined by quantitative polymerase chain reaction.
Kemppainen R; Hämäläinen ER; Kuivaniemi H; Tromp G; Pihlajaniemi T; Kivirikko KI
Arch Biochem Biophys; 1996 Apr; 328(1):101-6. PubMed ID: 8638917
[TBL] [Abstract][Full Text] [Related]
4. Severe congenital cutis laxa: Identification of novel homozygous LOX gene variants in two families.
McKenzie F; Mina K; Callewaert B; Beyens A; Dickinson JE; Jevon G; Papadimitriou J; Diness BR; Steensberg JN; Ek J; Baynam G
Clin Genet; 2021 Aug; 100(2):168-175. PubMed ID: 33866545
[TBL] [Abstract][Full Text] [Related]
5. Congenital cutis laxa syndrome: type II autosomal recessive inheritance.
Tüysüz B; Arapoğlu M; Ilikkan B; Demirkesen C; Perk Y
Turk J Pediatr; 2003; 45(3):265-8. PubMed ID: 14696810
[TBL] [Abstract][Full Text] [Related]
6. Congenital cutis laxa with retardation of growth and development.
Patton MA; Tolmie J; Ruthnum P; Bamforth S; Baraitser M; Pembrey M
J Med Genet; 1987 Sep; 24(9):556-61. PubMed ID: 3669050
[TBL] [Abstract][Full Text] [Related]
7. Severe congenital cutis laxa with pulmonary emphysema: a family with three affected sibs.
Van Maldergem L; Vamos E; Liebaers I; Petit P; Vandevelde G; Simonis-Blumenfrucht A; Bouffioux R; Kulakowski S; Hanquinet S; Van Durme P
Am J Med Genet; 1988 Oct; 31(2):455-64. PubMed ID: 3232707
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. Syndrome of congenital cutis laxa with ligamentous laxity and delayed development: report of a brother and sister from Turkey.
Oğur G; Yüksel-Apak M; Demiryont M
Am J Med Genet; 1990 Sep; 37(1):6-9. PubMed ID: 1700609
[TBL] [Abstract][Full Text] [Related]
10. Type II autosomal recessive cutis laxa: report of another patient and molecular studies concerning three candidate genes.
Scherrer DZ; Alexandrino F; Cintra ML; Sartorato EL; Steiner CE
Am J Med Genet A; 2008 Nov; 146A(21):2740-5. PubMed ID: 18819152
[TBL] [Abstract][Full Text] [Related]
11. Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica.
Kariminejad A; Afroozan F; Bozorgmehr B; Ghanadan A; Akbaroghli S; Khorram Khorshid HR; Mojahedi F; Setoodeh A; Loh A; Tan YX; Escande-Beillard N; Malfait F; Reversade B; Gardeitchik T; Morava E
Int J Mol Sci; 2017 Mar; 18(3):. PubMed ID: 28294978
[TBL] [Abstract][Full Text] [Related]
12. Male with type II autosomal recessive cutis laxa.
Imaizumi K; Kurosawa K; Makita Y; Masuno M; Kuroki Y
Clin Genet; 1994 Jan; 45(1):40-3. PubMed ID: 8149651
[TBL] [Abstract][Full Text] [Related]
13. Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation.
Morava E; Lefeber DJ; Urban Z; de Meirleir L; Meinecke P; Gillessen Kaesbach G; Sykut-Cegielska J; Adamowicz M; Salafsky I; Ranells J; Lemyre E; van Reeuwijk J; Brunner HG; Wevers RA
Eur J Hum Genet; 2008 Jan; 16(1):28-35. PubMed ID: 17971833
[TBL] [Abstract][Full Text] [Related]
14. Autosomal recessive form of congenital cutis laxa: more than the clinical appearance.
Andiran N; Sarikayalar F; Saraçlar M; Cağlar M
Pediatr Dermatol; 2002; 19(5):412-4. PubMed ID: 12383097
[TBL] [Abstract][Full Text] [Related]
15. A skeletal and connective tissue disorder associated with lysyl oxidase deficiency and abnormal copper metabolism.
Kaitila II; Peltonen L; Kuivaniemi H; Palotie A; Elo J; Kivirikko KI
Prog Clin Biol Res; 1982; 104():307-15. PubMed ID: 6131429
[No Abstract] [Full Text] [Related]
16. Cutis laxa of the autosomal recessive type in a consanguineous family.
de Schepper S; Loeys B; de Paepe A; Lambert J; Naeyaert JM
Eur J Dermatol; 2003; 13(6):529-33. PubMed ID: 14721770
[TBL] [Abstract][Full Text] [Related]
17. Congenital cutis laxa with a dominant inheritance and early onset emphysema.
Corbett E; Glaisyer H; Chan C; Madden B; Khaghani A; Yacoub M
Thorax; 1994 Aug; 49(8):836-7. PubMed ID: 8091333
[TBL] [Abstract][Full Text] [Related]
18. Epigenetic silencing of lysyl oxidase-like-1 through DNA hypermethylation in an autosomal recessive cutis laxa case.
Debret R; Cenizo V; Aimond G; André V; Devillers M; Rouvet I; Mégarbané A; Damour O; Sommer P
J Invest Dermatol; 2010 Nov; 130(11):2594-601. PubMed ID: 20613779
[TBL] [Abstract][Full Text] [Related]
19. An X-linked form of cutis laxa due to deficiency of lysyl oxidase.
Byers PH; Narayanan AS; Bornstein P; Hall JG
Birth Defects Orig Artic Ser; 1976; 12(5):293-8. PubMed ID: 953234
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]