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27. Clinical phenotype of Bart's syndrome seen in a family with dominant dystrophic epidermolysis bullosa. Wakasugi S; Mizutari K; Ono T J Dermatol; 1998 Aug; 25(8):517-22. PubMed ID: 9769597 [TBL] [Abstract][Full Text] [Related]
28. A novel glycine mutation in the COL7A1 gene leading to dominant dystrophic epidermolysis bullosa with intra-familial phenotypical heterogeneity. Riedl E; Klausegger A; Bauer JW; Foedinger D; Kittler H Pediatr Dermatol; 2009; 26(1):115-7. PubMed ID: 19250433 [TBL] [Abstract][Full Text] [Related]
29. Cerebellar ataxia in a family with recurrent epidermolysis bullosa dystrophica. Colombi M; Gardella R; Barlati S; Cappa SF; Marini D; Gasparotti R Arch Dermatol; 1991 Nov; 127(11):1737. PubMed ID: 1952992 [No Abstract] [Full Text] [Related]
30. Squamous cell carcinoma complicating epidermolysis bullosa in a 6-year-old girl. Shivaswamy KN; Sumathy TK; Shyamprasad AL; Ranganathan C Int J Dermatol; 2009 Jul; 48(7):731-3. PubMed ID: 19570079 [TBL] [Abstract][Full Text] [Related]
31. A Japanese family with dominant pretibial dystrophic epidermolysis bullosa: Identification of a new glycine substitution in the triple-helical collagenous domain of type VII collagen. Hamada T; Fukuda S; Ishii N; Abe T; Nagata K; Koro O; Hatano Y; Nakano H; Sawamura D; Hashimoto T J Dermatol Sci; 2009 Jun; 54(3):212-4. PubMed ID: 19269793 [No Abstract] [Full Text] [Related]
32. Congenital localized absence of skin, blistering and nail abnormalities, a new syndrome. Bart BJ Birth Defects Orig Artic Ser; 1971 Jun; 7(8):118-20. PubMed ID: 5173254 [TBL] [Abstract][Full Text] [Related]
33. Dominant dystrophic epidermolysis bullosa associated with pyloric stenosis and congenital absence of skin. Dereure O; Vailly J; Lagrange B; Meneguzzi G; Ortonne JP; Guillot B Arch Dermatol; 2001 May; 137(5):665-6. PubMed ID: 11346353 [No Abstract] [Full Text] [Related]
34. Images in HIV/AIDS. Elephantiasis nostras verrucosa secondary to Kaposi sarcoma: a rare case. Sathyakumar S; Suh JS; Sharp VL; Polsky B AIDS Read; 2008 Feb; 18(2):81-2. PubMed ID: 18330034 [No Abstract] [Full Text] [Related]
35. Recessive dystrophic epidermolysis bullosa complicated with nephrotic syndrome due to secondary amyloidosis. Gündüz K; Vatansever S; Türel A; Sen S Int J Dermatol; 2000 Feb; 39(2):151-3. PubMed ID: 10692067 [No Abstract] [Full Text] [Related]
36. A rare case of recessive dystrophic epidermolysis bullosa and verruciform xanthoma. Orpin SD; Scott IC; Rajaratnam R; Colloby PS; Heagerty A Clin Exp Dermatol; 2009 Jan; 34(1):49-51. PubMed ID: 18681870 [TBL] [Abstract][Full Text] [Related]
38. [Manifestations of epidermolysis bullosa in the deglutition tract]. Stĕdrý V; Síbl O; Hájek M Cesk Otolaryngol; 1990 Aug; 39(4):199-203. PubMed ID: 2289241 [TBL] [Abstract][Full Text] [Related]
39. Recessive dystrophic epidermolysis bullosa associated with mesangioproliferative glomerulonephritis and multifocal necrotizing leucoencephalopathy of the pons. Lehman TD; Morgan TK; Lehman NL; Vogel H; McGuire JS Br J Dermatol; 2004 Dec; 151(6):1266-9. PubMed ID: 15606525 [TBL] [Abstract][Full Text] [Related]
40. Glycine substitution mutations by different amino acids at the same codon in COL7A1 cause different modes of dystrophic epidermolysis bullosa inheritance. Sawamura D; Mochitomi Y; Kanzaki T; Nakamura H; Shimizu H Br J Dermatol; 2006 Oct; 155(4):834-7. PubMed ID: 16965438 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]