231 related articles for article (PubMed ID: 10905086)
1. [Occurrence of X-linked ichthyosis along with atopy].
Harangi F; Morava E; Adonyi M
Orv Hetil; 2000 Jun; 141(23):1301-3. PubMed ID: 10905086
[TBL] [Abstract][Full Text] [Related]
2. X-linked ichthyosis without STS deficiency: clinical, genetical, and molecular studies.
Robledo R; Melis P; Schillinger E; Casciano I; Balazs I; Rinaldi A; Siniscalco M; Filippi G
Am J Med Genet; 1995 Nov; 59(2):143-8. PubMed ID: 8588575
[TBL] [Abstract][Full Text] [Related]
3. Allergic disease as an association of steroid sulphatase deficiency.
Sakura N; Nishimura S; Matsumoto T; Ohsaki M; Ogata T
J Inherit Metab Dis; 1997 Nov; 20(6):807-10. PubMed ID: 9427150
[TBL] [Abstract][Full Text] [Related]
4. Characterization of the deletion breakpoints in a patient with steroid sulfatase deficiency.
Yen PH; Ferrero GB; Chinault AC; Mohandas T; Ballabio A
Hum Mutat; 1994; 4(1):76-8. PubMed ID: 7951263
[No Abstract] [Full Text] [Related]
5. Delay of growth and development in children with bronchial asthma, atopic dermatitis and allergic rhinitis.
Baum WF; Schneyer U; Lantzsch AM; Klöditz E
Exp Clin Endocrinol Diabetes; 2002 Apr; 110(2):53-9. PubMed ID: 11928066
[TBL] [Abstract][Full Text] [Related]
6. Somatic and germinal mosaicism for the steroid sulfatase gene deletion in a steroid sulfatase deficiency carrier.
Cuevas-Covarrubias SA; Jiménez-Vaca AL; González-Huerta LM; Valdes-Flores M; Del Refugio Rivera-Vega M; Maya-Nunez G; Kofman-Alfaro SH
J Invest Dermatol; 2002 Oct; 119(4):972-5. PubMed ID: 12406347
[TBL] [Abstract][Full Text] [Related]
7. Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X-linked ichthyosis due to steroid sulfatase deficiency.
Ballabio A; Zollo M; Carrozzo R; Caiulo A; Zuffardi O; Cascioli CF; Viggiano D; Strisciuglio P
Am J Med Genet; 1991 Nov; 41(2):184-7. PubMed ID: 1785631
[TBL] [Abstract][Full Text] [Related]
8. The biochemical identification of carrier state in mothers of sporadic cases of X-linked recessive ichthyosis.
Cuevas-Covarrubias SA; Kofman-Alfaro S; Orozco Orozco E; Diaz-Zagoya JC
Genet Couns; 1995; 6(2):103-7. PubMed ID: 7546451
[TBL] [Abstract][Full Text] [Related]
9. X-linked ichthyosis: an update.
Hernández-Martín A; González-Sarmiento R; De Unamuno P
Br J Dermatol; 1999 Oct; 141(4):617-27. PubMed ID: 10583107
[TBL] [Abstract][Full Text] [Related]
10. Two cases of steroid sulfatase deficiency with complex phenotype due to contiguous gene deletions.
Nishimura S; Masuda H; Matsumoto T; Sakura N; Matsumoto T; Ueda K
Am J Med Genet; 1991 Sep; 40(3):260-3. PubMed ID: 1951426
[TBL] [Abstract][Full Text] [Related]
11. Most "sporadic" cases of X-linked ichthyosis are not de novo mutations.
Cuevas-Covarrubias SA; Valdes-Flores M; Orozco Orozco E; Díaz-Zagoya JC; Kofman-Alfaro SH
Acta Derm Venereol; 1999 Mar; 79(2):143-4. PubMed ID: 10228635
[TBL] [Abstract][Full Text] [Related]
12. The detection of steroid sulfatase gene deletion (STS) in Egyptian males with X-linked ichthyosis.
Abdel-Hamed MF; Hussein HA; Helmy NA; Elsaie ML
J Drugs Dermatol; 2010 Oct; 9(10):1192-6. PubMed ID: 20941942
[TBL] [Abstract][Full Text] [Related]
13. Association of atopy, asthma, allergic rhinoconjunctivitis, atopic dermatitis and intestinal helminth infections in Cuban children.
Wördemann M; Diaz RJ; Heredia LM; Collado Madurga AM; Ruiz Espinosa A; Prado RC; Millan IA; Escobedo A; Rojas Rivero L; Gryseels B; Gorbea MB; Polman K
Trop Med Int Health; 2008 Feb; 13(2):180-6. PubMed ID: 18304263
[TBL] [Abstract][Full Text] [Related]
14. [Two cases of X-linked ichthyosis associated with myopathies].
Ishikawa Y; Imai T; Kameda K; Okabe M; Nagaoka M; Minami R
Rinsho Shinkeigaku; 1990 Aug; 30(8):855-9. PubMed ID: 2253421
[TBL] [Abstract][Full Text] [Related]
15. Deletion of exons 1-5 of the STS gene causing X-linked ichthyosis.
Valdes-Flores M; Kofman-Alfaro SH; Vaca AL; Cuevas-Covarrubias SA
J Invest Dermatol; 2001 Mar; 116(3):456-8. PubMed ID: 11231321
[TBL] [Abstract][Full Text] [Related]
16. Atopic cataracts in a Japanese population. With special reference to factors possibly relevant to cataract formation.
Uehara M; Amemiya T; Arai M
Dermatologica; 1985; 170(4):180-4. PubMed ID: 3996701
[TBL] [Abstract][Full Text] [Related]
17. [Biochemical study on steroid sulfatase and its clinical application to the obstetrics and gynecology].
Sugawara T
Hokkaido Igaku Zasshi; 1992 Jul; 67(4):552-62. PubMed ID: 1427599
[TBL] [Abstract][Full Text] [Related]
18. Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsy.
Gohlke BC; Haug K; Fukami M; Friedl W; Noeker M; Rappold GA; Haverkamp F
J Med Genet; 2000 Aug; 37(8):600-2. PubMed ID: 10922387
[TBL] [Abstract][Full Text] [Related]
19. A study of the steroid sulfatase gene in families with X-linked ichthyosis using polymerase chain reaction.
Nomura K; Nakano H; Umeki K; Harada K; Kon A; Tamai K; Sawamura D; Hashimoto I
Acta Derm Venereol; 1995 Sep; 75(5):340-2. PubMed ID: 8615047
[TBL] [Abstract][Full Text] [Related]
20. Deletion patterns of the STS gene and flanking sequences in Israeli X-linked ichthyosis patients and carriers: analysis by polymerase chain reaction and fluorescence in situ hybridization techniques.
Aviram-Goldring A; Goldman B; Netanelov-Shapira I; Chen-Shtoyerman R; Zvulunov A; Tal O; Ilan T; Peleg L
Int J Dermatol; 2000 Mar; 39(3):182-7. PubMed ID: 10759956
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]