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26. Deep Phenotyping of Superficial Epidermolytic Ichthyosis due to a Recurrent Mutation in KRT2. Suzuki Y, Takeichi T, Tanahashi K, Muro Y, Suga Y, Ogi T, Akiyama M. Int J Mol Sci; 2022 Jul 14; 23(14):. PubMed ID: 35887135 [Abstract] [Full Text] [Related]
27. [A case of congenital ichthyosiform erythroderma of Brocq with universal edema]. GROSS H. Arch Kinderheilkd; 1954 Jul 14; 149(1):72-5. PubMed ID: 13218627 [No Abstract] [Full Text] [Related]
28. Bullous congenital ichthyosiform erythroderma of Brocq. Kucharekova M, Mosterd K, Winnepenninckx V, van Geel M, Sommer A, van Steensel MA. Int J Dermatol; 2007 Nov 14; 46 Suppl 3():36-8. PubMed ID: 17973888 [Abstract] [Full Text] [Related]
29. Dyskeratosis ichthyosiformis congenita migrans: a variant of congenital ichthyosiform erythroderma. STEVANOVIC DV, PAVIC RL. AMA Arch Derm; 1958 Nov 14; 78(5):625-9. PubMed ID: 13582209 [No Abstract] [Full Text] [Related]
30. [CONGENITAL ICHTHYOSIFORM ERYTHRODERMA ASSOCIATED WITH SYMBLEPHARON AND KERATODYSTROPHY]. LANCELLOTTI M, TABACCHI G. Minerva Dermatol; 1964 Dec 14; 39():335-42. PubMed ID: 14265264 [No Abstract] [Full Text] [Related]