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2. [The cytoskeleton in hereditary ichthyoses]. Moll I, Traupe H, Voigtländer V, Moll R. Hautarzt; 1988 Feb; 39(2):82-90. PubMed ID: 2452141 [Abstract] [Full Text] [Related]
3. [Hereditary ichthyosis in Tunisia: epidemiological study of 60 cases]. Kharfi M, El Fekih N, Ammar D, Khaled A, Fazaa B, Ridha Kamoun M. Tunis Med; 2008 Nov; 86(11):983-6. PubMed ID: 19213489 [Abstract] [Full Text] [Related]
4. Ichthyosis: etiology, diagnosis, and management. DiGiovanna JJ, Robinson-Bostom L. Am J Clin Dermatol; 2003 Nov; 4(2):81-95. PubMed ID: 12553849 [Abstract] [Full Text] [Related]
5. The expression of the 27-kd heat shock protein in keratinization disorders: an immunohistological study. Jonak C, Metze D, Traupe H, Happle R, König A, Trautinger F. Hum Pathol; 2005 Jun; 36(6):686-93. PubMed ID: 16021576 [Abstract] [Full Text] [Related]
7. Ichthyosis: clinical manifestations and practical treatment options. Oji V, Traupe H. Am J Clin Dermatol; 2009 Jun; 10(6):351-64. PubMed ID: 19824737 [Abstract] [Full Text] [Related]
8. Autosomal dominant lamellar ichthyosis: a new skin disorder. Traupe H, Kolde G, Happle R. Clin Genet; 1984 Nov; 26(5):457-61. PubMed ID: 6499258 [Abstract] [Full Text] [Related]
9. [Serum IgE level in autosomal dominant and X chromosomal recessive ichthyosis vulgaris]. Würsch TG, Wüthrich B. Z Hautkr; 1980 Dec 15; 55(24):1615-9. PubMed ID: 7194545 [Abstract] [Full Text] [Related]
10. Elevated n-alkanes in congenital ichthyosiform erythroderma. Phenotypic differentiation of two types of autosomal recessive ichthyosis. Williams ML, Elias PM. J Clin Invest; 1984 Jul 15; 74(1):296-300. PubMed ID: 6736251 [Abstract] [Full Text] [Related]
12. Report of a family with an unusual expression of recessive ichthyosis. Review of 42 cases. Bernhardt M, Baden HP. Arch Dermatol; 1986 Apr 15; 122(4):428-33. PubMed ID: 3954411 [Abstract] [Full Text] [Related]
13. Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009. Oji V, Tadini G, Akiyama M, Blanchet Bardon C, Bodemer C, Bourrat E, Coudiere P, DiGiovanna JJ, Elias P, Fischer J, Fleckman P, Gina M, Harper J, Hashimoto T, Hausser I, Hennies HC, Hohl D, Hovnanian A, Ishida-Yamamoto A, Jacyk WK, Leachman S, Leigh I, Mazereeuw-Hautier J, Milstone L, Morice-Picard F, Paller AS, Richard G, Schmuth M, Shimizu H, Sprecher E, Van Steensel M, Taïeb A, Toro JR, Vabres P, Vahlquist A, Williams M, Traupe H. J Am Acad Dermatol; 2010 Oct 15; 63(4):607-41. PubMed ID: 20643494 [Abstract] [Full Text] [Related]
14. [Genetic counseling in Sjögren-Larsson syndrome (author's transl)]. Theile U. Z Orthop Ihre Grenzgeb; 1978 Oct 15; 116(6):912-4. PubMed ID: 726579 [Abstract] [Full Text] [Related]
15. Inherited ichthyosis: Syndromic forms. Yoneda K. J Dermatol; 2016 Mar 15; 43(3):252-63. PubMed ID: 26945533 [Abstract] [Full Text] [Related]
16. Clinico-epidemiological features of primary hereditary ichthyoses in the Eastern province of Saudi Arabia. Al-Zayir AA, Al-Amro Al-Alakloby OM. Int J Dermatol; 2006 Mar 15; 45(3):257-64. PubMed ID: 16533225 [Abstract] [Full Text] [Related]
17. [Sjögren-Larsson syndrome: lamellar ichthyosis, mental retardation and spasticity (author's transl)]. Ruiz Maldonado R, Tamayo L, Carnevale A, López A, Peña L. Rev Invest Clin; 1974 Mar 15; 26(1):63-74. PubMed ID: 4453676 [No Abstract] [Full Text] [Related]
18. Possible genetic heterogeneity of X-linked ichthyosis. Passarge E, Post B, Schöpf E. Birth Defects Orig Artic Ser; 1971 Jun 15; 7(8):46-9. PubMed ID: 5173313 [Abstract] [Full Text] [Related]
19. Ichthyosis and neutral lipid storage disease. Williams ML, Koch TK, O'Donnell JJ, Frost PH, Epstein LB, Grizzard WS, Epstein CJ. Am J Med Genet; 1985 Apr 15; 20(4):711-26. PubMed ID: 3993689 [Abstract] [Full Text] [Related]
20. A mother and two children with nonbullous congenital ichthyosiform erythroderma. Rossmann-Ringdahl I, Anton-Lamprecht I, Swanbeck G. Arch Dermatol; 1986 May 15; 122(5):559-64. PubMed ID: 3707173 [Abstract] [Full Text] [Related] Page: [Next] [New Search]