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27. The phenotypic heterogenicity of bullous ichthyosis--a case report of three family members. McGrath J; Cerio R; Wilson-Jones E Clin Exp Dermatol; 1991 Jan; 16(1):25-7. PubMed ID: 2025929 [TBL] [Abstract][Full Text] [Related]
28. Genetically induced abnormalities of epidermal differentiation and ultrastructure in ichthyoses and epidermolyses: pathogenesis, heterogeneity, fetal manifestation, and prenatal diagnosis. Anton-Lamprecht I J Invest Dermatol; 1983 Jul; 81(1 Suppl):149s-56s. PubMed ID: 6345689 [TBL] [Abstract][Full Text] [Related]
30. Epidermolytic Hyperkeratosis--case report. Hayashida MT; Mitsui GL; Reis NI; Fantinato G; Jordão Neto D; Mercante AM An Bras Dermatol; 2015; 90(6):888-91. PubMed ID: 26734873 [TBL] [Abstract][Full Text] [Related]
31. Mutations in the rod domain of keratin 2e in patients with ichthyosis bullosa of Siemens. Rothnagel JA; Traupe H; Wojcik S; Huber M; Hohl D; Pittelkow MR; Saeki H; Ishibashi Y; Roop DR Nat Genet; 1994 Aug; 7(4):485-90. PubMed ID: 7524919 [TBL] [Abstract][Full Text] [Related]
32. "Blind" versus direct vision technique for fetal skin sampling in cases for prenatal diagnosis. Löfberg L; Gustavii B Clin Genet; 1984 Jan; 25(1):37-41. PubMed ID: 6368057 [TBL] [Abstract][Full Text] [Related]
33. Selective involvement of keratins K1 and K10 in the cytoskeletal abnormality of epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma). Ishida-Yamamoto A; McGrath JA; Judge MR; Leigh IM; Lane EB; Eady RA J Invest Dermatol; 1992 Jul; 99(1):19-26. PubMed ID: 1376754 [TBL] [Abstract][Full Text] [Related]
34. A new keratin 2e mutation in ichthyosis bullosa of Siemens. Jones DO; Watts C; Mills C; Sharpe G; Marks R; Bowden PE J Invest Dermatol; 1997 Mar; 108(3):354-6. PubMed ID: 9036938 [TBL] [Abstract][Full Text] [Related]
35. Superficial epidermolytic ichthyosis: a report of two families. Cervantes T; Pham C; Browning JC Pediatr Dermatol; 2013; 30(4):469-72. PubMed ID: 22612346 [TBL] [Abstract][Full Text] [Related]
36. Ichthyosis bullosa of Siemens resulting from a novel missense mutation near the helix termination motif of the keratin 2e gene. Moraru R; Cserhalmi-Friedman PB; Grossman ME; Schneiderman P; Christiano AM Clin Exp Dermatol; 1999 Sep; 24(5):412-5. PubMed ID: 10564334 [TBL] [Abstract][Full Text] [Related]
37. A novel helix termination mutation in keratin 10 in annular epidermolytic ichthyosis, a variant of bullous congenital ichthyosiform erythroderma. Suga Y; Duncan KO; Heald PW; Roop DR J Invest Dermatol; 1998 Dec; 111(6):1220-3. PubMed ID: 9856845 [TBL] [Abstract][Full Text] [Related]
38. Prenatal diagnosis of congenital bullous ichthyosiform erythroderma (epidermolytic hyperkeratosis) by fetal skin biopsy. Golbus MS; Sagebiel RW; Filly RA; Gindhart TD; Hall JG N Engl J Med; 1980 Jan; 302(2):93-5. PubMed ID: 6985700 [No Abstract] [Full Text] [Related]
39. How do keratinizing disorders and blistering disorders overlap? Hamada T; Tsuruta D; Fukuda S; Ishii N; Teye K; Numata S; Dainichi T; Karashima T; Ohata C; Furumura M; Hashimoto T Exp Dermatol; 2013 Feb; 22(2):83-7. PubMed ID: 23039137 [TBL] [Abstract][Full Text] [Related]
40. Treating epidermolytic ichthyosis and ichthyosis with confetti with epidermal autografts cultured from revertant skin. Tanahashi K; Kono M; Yoshikawa T; Suzuki Y; Inoie M; Kuwatsuka Y; Kinoshita F; Takeichi T; Akiyama M Br J Dermatol; 2024 Aug; 191(3):397-404. PubMed ID: 38739763 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]