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22. [Probable liaison between loci of genes causing 2 recessive autosomic diseases: dystrophic bullous epidermolysis and mesenteric lymphangiectasia. Apropos of a case]. Macotela-Ruiz E; Cantu JM; Landa L; Ancona A Bull Soc Fr Dermatol Syphiligr; 1969; 76(6):771-3. PubMed ID: 5384199 [No Abstract] [Full Text] [Related]
23. [Contribution of a case on epidermolysis bullosa hereditaria dystrophica, albopapuloid type of Pasini]. Metzner HH Dermatol Wochenschr; 1967 Sep; 153(39):1081-6. PubMed ID: 5613996 [No Abstract] [Full Text] [Related]
24. Cause-specific risks of childhood death in inherited epidermolysis bullosa. Fine JD; Johnson LB; Weiner M; Suchindran C J Pediatr; 2008 Feb; 152(2):276-80. PubMed ID: 18206702 [TBL] [Abstract][Full Text] [Related]
25. [Antenatal diagnosis of hereditary epidermolysis bullosa]. Blanchet-Bardon C; Dumez Y; Nazzaro V; Mimoz C; Puissant A Ann Dermatol Venereol; 1987; 114(4):525-39. PubMed ID: 3619299 [TBL] [Abstract][Full Text] [Related]
27. Progress in epidermolysis bullosa: from eponyms to molecular genetic classification. Uitto J; Richard G Clin Dermatol; 2005; 23(1):33-40. PubMed ID: 15708287 [TBL] [Abstract][Full Text] [Related]
28. Epidermolysis bullosa. Lin AN; Carter DM Annu Rev Med; 1993; 44():189-99. PubMed ID: 8476240 [TBL] [Abstract][Full Text] [Related]
29. Enhanced biosynthesis of human skin collagenase in fibroblast cultures from recessive dystrophic epidermolysis bullosa. Valle KJ; Bauer EA J Clin Invest; 1980 Aug; 66(2):176-87. PubMed ID: 6249847 [TBL] [Abstract][Full Text] [Related]
30. Gastrointestinal complications of inherited epidermolysis bullosa: cumulative experience of the National Epidermolysis Bullosa Registry. Fine JD; Johnson LB; Weiner M; Suchindran C J Pediatr Gastroenterol Nutr; 2008 Feb; 46(2):147-58. PubMed ID: 18223373 [TBL] [Abstract][Full Text] [Related]
31. Gastrointestinal manifestations of epidermolysis bullosa in children. Gryboski JD; Touloukian R; Campanella RA Arch Dermatol; 1988 May; 124(5):746-52. PubMed ID: 3364997 [TBL] [Abstract][Full Text] [Related]
33. Compound heterozygosity for a nonsense mutation and a splice site mutation in the type VII collagen gene (COL7A1) in recessive dystrophic epidermolysis bullosa. Tamai K; Ishida-Yamamoto A; Matsuo S; Iizuka H; Hashimoto I; Christiano AM; Uitto J; McGrath JA Lab Invest; 1997 Feb; 76(2):209-17. PubMed ID: 9042157 [TBL] [Abstract][Full Text] [Related]
34. [Recessive dystrophic epidermolysis bullosa (with esophageal involvement)]. Vallarino J; Terán de Vallarino M; Ollague W; Macias J; Jalil A Med Cutan Ibero Lat Am; 1986; 14(1):19-25. PubMed ID: 3526033 [TBL] [Abstract][Full Text] [Related]
35. [Hereditary epidermolysis bullosa in Tunisia: an epidemio-clinical and ultrastructural study]. Cherif F; Mnajja N; Feriani S; Ben Saïd ZM; Jaafoura MH; Dhahri AB; Boubaker S Arch Inst Pasteur Tunis; 2005; 82(1-4):53-8. PubMed ID: 16929755 [TBL] [Abstract][Full Text] [Related]
36. [Simple epidermolysis bullosa. A case in twins]. Goberna F; Martínez M; Arribas M; Galparsoro JM; Ruiz C; Ruiz JM; Sanz M An Esp Pediatr; 1986 Feb; 24(2):131-3. PubMed ID: 3963654 [No Abstract] [Full Text] [Related]
38. Premature termination codon mutations in the type VII collagen gene (COL7A1) underlie severe recessive dystrophic epidermolysis bullosa. Uitto J; Hovnanian A; Christiano AM Proc Assoc Am Physicians; 1995 Jul; 107(2):245-52. PubMed ID: 8624860 [No Abstract] [Full Text] [Related]
39. Eye involvement in inherited epidermolysis bullosa: experience of the National Epidermolysis Bullosa Registry. Fine JD; Johnson LB; Weiner M; Stein A; Cash S; Deleoz J; Devries DT; Suchindran C Am J Ophthalmol; 2004 Aug; 138(2):254-62. PubMed ID: 15289135 [TBL] [Abstract][Full Text] [Related]