X연관 어린선 (Korean Wikipedia)

Analysis of information sources in references of the Wikipedia article "X연관 어린선" in Korean language version.

refsWebsite

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11nih.gov

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7doi.org

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2pnas.org

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1omim.org

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1emedicine.com

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1ablenews.co.kr

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1docdocdoc.co.kr

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1oxfordjournals.org

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ablenews.co.kr

http://www.ablenews.co.kr/News/NewsContent.aspx?CategoryCode=0023&NewsCode=002320090731210833656250

docdocdoc.co.kr

http://www.docdocdoc.co.kr/news/newsview.php?newscd=2013052800041

doi.org

dx.doi.org

Ballabio A; Parenti G; Carrozzo R; 외. (1987). “Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis”. 《Proc. Natl. Acad. Sci. U.S.A.》 84 (13): 4519–23. doi:10.1073/pnas.84.13.4519. PMC 305121. PMID 3474618.
Bonifas JM; Morley BJ; Oakey RE; Kan YW; Epstein EH (1987년 12월). “Cloning of a cDNA for steroid sulfatase: frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosis”. 《Proc. Natl. Acad. Sci. U.S.A.》 84 (24): 9248–51. doi:10.1073/pnas.84.24.9248. PMC 299730. PMID 3480541.
Lykkesfeldt G; Lykkesfeldt AE; Skakkebaek NE (1984). “Steroid sulphatase in man: a non inactivated X-locus with partial gene dosage compensation”. 《Hum. Genet.》 65 (4): 355–7. doi:10.1007/BF00291559. PMID 6582028.
Van Esch H; Hollanders K; Badisco L; 외. (2005). “Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis”. 《Hum. Mol. Genet.》 14 (13): 1795–803. doi:10.1093/hmg/ddi186. PMID 15888481.
Ballabio A; Sebastio G; Carrozzo R; 외. (1987). “Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndrome”. 《Hum. Genet.》 77 (4): 338–41. doi:10.1007/BF00291422. PMID 3480263.
Cotellessa C; Cuevas-Covarrubias SA; Valeri P; Fargnoli MC; Peris K (2005). “Topical tazarotene 0.05% versus glycolic acid 70% treatment in X-linked ichthyosis due to extensive deletion of the STS gene”. 《Acta Derm. Venereol.》 85 (4): 346–8. doi:10.1080/00015550510026613. PMID 16191859.
Freiberg RA; Choate KA; Deng H; Alperin ES; Shapiro LJ; Khavari PA (1997). “A model of corrective gene transfer in X-linked ichthyosis”. 《Hum. Mol. Genet.》 6 (6): 927–33. doi:10.1093/hmg/6.6.927. PMID 9175741.

emedicine.com

Ichthyosis, X-Linked - eMedicine: Treatment Section

nih.gov

ncbi.nlm.nih.gov

Ballabio A; Parenti G; Carrozzo R; 외. (1987). “Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis”. 《Proc. Natl. Acad. Sci. U.S.A.》 84 (13): 4519–23. doi:10.1073/pnas.84.13.4519. PMC 305121. PMID 3474618.
Bonifas JM; Morley BJ; Oakey RE; Kan YW; Epstein EH (1987년 12월). “Cloning of a cDNA for steroid sulfatase: frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosis”. 《Proc. Natl. Acad. Sci. U.S.A.》 84 (24): 9248–51. doi:10.1073/pnas.84.24.9248. PMC 299730. PMID 3480541.
Basler E; Grompe M; Parenti G; Yates J; Ballabio A (1992년 3월). “Identification of point mutations in the steroid sulfatase gene of three patients with X-linked ichthyosis”. 《Am. J. Hum. Genet.》 50 (3): 483–91. PMC 1684279. PMID 1539590.
Cuevas-Covarrubias SA; Kofman-Alfaro S; Orozco Orozco E,; Diaz-Zagoya JC (1995). “The biochemical identification of carrier state in mothers of sporadic cases of X-linked recessive ichthyosis”. 《Genet. Couns.》 6 (2): 103–7. PMID 7546451.
Lykkesfeldt G; Lykkesfeldt AE; Skakkebaek NE (1984). “Steroid sulphatase in man: a non inactivated X-locus with partial gene dosage compensation”. 《Hum. Genet.》 65 (4): 355–7. doi:10.1007/BF00291559. PMID 6582028.
DiGiovanna JJ, Robinson-Bostom L (2003). “Ichthyosis: etiology, diagnosis, and management”. 《Am J Clin Dermatol》 4 (2): 81–95. PMID 12553849.
Van Esch H; Hollanders K; Badisco L; 외. (2005). “Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis”. 《Hum. Mol. Genet.》 14 (13): 1795–803. doi:10.1093/hmg/ddi186. PMID 15888481.
Ballabio A; Sebastio G; Carrozzo R; 외. (1987). “Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndrome”. 《Hum. Genet.》 77 (4): 338–41. doi:10.1007/BF00291422. PMID 3480263.
Bradshaw KD; Carr BR (1986). “Placental sulfatase deficiency: maternal and fetal expression of steroid sulfatase deficiency and X-linked ichthyosis”. 《Obstet Gynecol Surv》 41 (7): 401–13. PMID 3531932.
Cotellessa C; Cuevas-Covarrubias SA; Valeri P; Fargnoli MC; Peris K (2005). “Topical tazarotene 0.05% versus glycolic acid 70% treatment in X-linked ichthyosis due to extensive deletion of the STS gene”. 《Acta Derm. Venereol.》 85 (4): 346–8. doi:10.1080/00015550510026613. PMID 16191859.
Freiberg RA; Choate KA; Deng H; Alperin ES; Shapiro LJ; Khavari PA (1997). “A model of corrective gene transfer in X-linked ichthyosis”. 《Hum. Mol. Genet.》 6 (6): 927–33. doi:10.1093/hmg/6.6.927. PMID 9175741.

omim.org

Online 'Mendelian Inheritance in Man' (OMIM) ICHTHYOSIS, X-LINKED -308100

oxfordjournals.org

hmg.oxfordjournals.org

Freiberg RA; Choate KA; Deng H; Alperin ES; Shapiro LJ; Khavari PA (1997). “A model of corrective gene transfer in X-linked ichthyosis”. 《Hum. Mol. Genet.》 6 (6): 927–33. doi:10.1093/hmg/6.6.927. PMID 9175741.

pnas.org

Ballabio A; Parenti G; Carrozzo R; 외. (1987). “Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis”. 《Proc. Natl. Acad. Sci. U.S.A.》 84 (13): 4519–23. doi:10.1073/pnas.84.13.4519. PMC 305121. PMID 3474618.
Bonifas JM; Morley BJ; Oakey RE; Kan YW; Epstein EH (1987년 12월). “Cloning of a cDNA for steroid sulfatase: frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosis”. 《Proc. Natl. Acad. Sci. U.S.A.》 84 (24): 9248–51. doi:10.1073/pnas.84.24.9248. PMC 299730. PMID 3480541.