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Bu Makaleye Atıf Yap
TEKİN, M., KAHRAMANER, Z., ERDEMİR, A., KONCA, Ç. (2022). Harlequin iktiyozis: Aynı ailede üçüncü olgu. Türk Pediatri Arşivi, Cilt: 49 - Sayı: 3, 269–271. https://ajindex.com/articles/641247
Dergiler / Türk Pediatri Arşivi / 2014 / Cilt: 49 - Sayı: 3
Harlequin iktiyozis: Aynı ailede üçüncü olgu
- Dergi
- Türk Pediatri Arşivi
- Sayfa
- 269–271
- Yayın Tarihi
- 2022-11-05
- DOI
- —
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DergiPark Kaydı ↗Kaynakça (3)
- Akiyama M, Sugiyama-Nakagiri Y, Sakai K, et al. Mutations in ipid transporter ABCA12 in harlequin ichthyosis and functio- nal recovery by corrective gene transfer. J Clin Invest 2005; 115: 1777-84. [CrossRef ] Darmstadt GL, Sidbury R. Disordersof keratinization. In: Behrman RE, Kliegman RM, Jenson HB, (eds). Nelson Textbook of Pediatrics. 17th ed. Philadelphia: WB Saunders Company, 2004: 2200-4.
- Milner ME, OGuin WM, Holbrook KA, Dale BA. Abnormal lamellar granules in harlequin ichthyosis. J Invest Dermatol. 1992; 99: 824-9. [CrossRef ] Akiyama M. The pathogenesis of severe congenital ichthyosis of the neonate. J Dermatol Sci 1999; 21: 96-104. [CrossRef ] Saraçoğlu ZN, Tekin N, Ürer SM, Sabuncu I, Akbit A. Oral acit- retin treatment in severe congenital ichthyosis of the neonate. Turk J Pediatr 2002; 44: 61-4.
- Rajpopat S, Moss C, Mellerio J, et al. Harlequin Ichthyosis: A Review of Clinical and Molecular Findings in 45 Cases. Arch Dermatol 2011; 147: 681-6. [CrossRef ] Richard G, Choate K, Milstone L, Bale S. Management of icthyo- sis and related conditions gene based diagnosis and emerging gene based therapy. Dermatol Ther 2013; 26: 55-68. [CrossRef ]