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5. [Phenytoin therapy in recessive dystrophic epidermolyses (epidermolysis bullosa dystrophica type Hallopeau-Siemens and epidermolysis bullosa dystrophica inversa)]. Wirth H; Nesch A; Ostapowicz B; Anton-Lamprecht I Z Hautkr; 1983 Apr; 58(8):555-74. PubMed ID: 6858283 [TBL] [Abstract][Full Text] [Related]
6. [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]
7. [Cockayne syndrome and epidermolysis bullosa dystrophica (Hallopeau-Siemens). Simultaneous occurrence in a family]. Lubach D; Riechers U Hautarzt; 1982 Sep; 33(9):491-4. PubMed ID: 7174321 [TBL] [Abstract][Full Text] [Related]
8. [Incidence of structural disorders of teeth in hereditary epidermolysis bullosa]. Gábris K; Csiba A; Orosz M Fogorv Sz; 1996 Jan; 89(1):7-10. PubMed ID: 8713615 [TBL] [Abstract][Full Text] [Related]
9. Epidermolysis bullosa (report of 7 cases in two families). Khatri ML; Jain ML; Charan SS; Mathur NK Indian J Dermatol; 1976 Jul; 21(4):71-3. PubMed ID: 1022691 [No Abstract] [Full Text] [Related]
10. [Gastrointestinal manifestations of recessive dystrophic epidermolysis bullosa]. Michel-Aceves R; Ramírez-Mayans JA; Casaubón-Garcín P; Rivera-Echegoyen M; Antonieta Mora M Bol Med Hosp Infant Mex; 1990 Jan; 47(1):20-5. PubMed ID: 2186753 [TBL] [Abstract][Full Text] [Related]
11. Epidermolysis bullosa simplex associated with muscular dystrophy with recessive inheritance. Niemi KM; Sommer H; Kero M; Kanerva L; Haltia M Arch Dermatol; 1988 Apr; 124(4):551-4. PubMed ID: 3355199 [TBL] [Abstract][Full Text] [Related]
12. Epidermolysis bullosa in Finland. Clinical features, morphology and relation to collagen metabolism. Kero M Acta Derm Venereol Suppl (Stockh); 1984; 110():1-51. PubMed ID: 6331034 [TBL] [Abstract][Full Text] [Related]
13. Epidermolysis bullosa dystrophica dominans in two families in the Faroe Islands. A clinico-genetic study of 56 living individuals. Joensen HD Acta Derm Venereol; 1973; 53(1):53-60. PubMed ID: 4120809 [No Abstract] [Full Text] [Related]
14. 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]
15. The largest family of the Americas with dominant dystrophic epidermolysis bullosa pruriginosa: a 18-year longitudinal genotype-phenotype study. Fortuna G; Di Lorenzo M; Cepeda-Valdes R; Garcia-Garcia C; Salas-Alanis JC J Dermatol Sci; 2013 Sep; 71(3):217-21. PubMed ID: 23688405 [No Abstract] [Full Text] [Related]
16. A rare complication of hereditary epidermolysis bullosa: esophageal carcinoma in recessive dystrophic epidermolysis bullosa inversa. Onsun N; Su O; Pirmit S; Korkmaz S; Korkut YA; Akaydin M; Arda N Eur J Dermatol; 2012; 22(3):409-10. PubMed ID: 22481021 [No Abstract] [Full Text] [Related]
17. [Biochemical and laboratory findings in epidermolysis bullosa hereditaria dystrophica et polydysplastica]. Kansky A G Ital Dermatol Minerva Dermatol; 1970 Mar; 45(3):176-9. PubMed ID: 5468547 [No Abstract] [Full Text] [Related]