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22. The Cockayne-Touraine type of dominant dystrophic epidermolysis bullosa--ultrastructural similarities to the Pasini variant. Oakley CA; Gawkrodger DJ; Ross JA; Hunter JA Acta Derm Venereol; 1984; 64(3):253-6. PubMed ID: 6204490 [TBL] [Abstract][Full Text] [Related]
23. [Dominant epidermolysis bullosa dystrophica of Cockayne-Touraine. Presentation of a familial case and cytogenetic investigation]. Amerio P; Pallotta R; Di Donato D; Dalprà L G Ital Dermatol Venereol; 1988 Sep; 123(9):417-20. PubMed ID: 3243581 [No Abstract] [Full Text] [Related]
24. [Bullae and blisters--differential diagnosis]. Schnopp C MMW Fortschr Med; 2007 Feb; 149(6):29-32. PubMed ID: 17619399 [TBL] [Abstract][Full Text] [Related]
25. [Hereditary epidermolysis bullosa. Epidemiology and clinical classification of 23 cases]. Zahaf A; Mkaouar M; Rebei R Arch Fr Pediatr; 1988 Dec; 45(10):795-8. PubMed ID: 3071287 [TBL] [Abstract][Full Text] [Related]
31. [Review of ophthalmologic complications in hereditary bullous epidermolysis. Apropos of 40 cases]. Deplus S; Bremond-Gignac D; Blanchet-Bardon C; Febrarro JL; Gaudric A J Fr Ophtalmol; 1999; 22(7):760-5. PubMed ID: 10510756 [TBL] [Abstract][Full Text] [Related]
32. Congenital localized absence of skin and associated abnormalities resembling epidermolysis bullosa. A new syndrome. Bart BJ; Gorlin RJ; Anderson VE; Lynch FW Arch Dermatol; 1966 Mar; 93(3):296-304. PubMed ID: 5910871 [No Abstract] [Full Text] [Related]
33. [Dowling-Meara dominant epidermolysis bullosa. An intraepidermal epidermolysis bullosa which hides its prognosis well]. Blanchet-Bardon C; Nazzaro V; Raynaud F; Hubert S; Mimoz C Ann Dermatol Venereol; 1987; 114(3):341-8. PubMed ID: 3605965 [TBL] [Abstract][Full Text] [Related]
34. [Epidermolysis bullosa acquisita: diagnosis by optic immunofluorescent demonstration of junctional antigens and vitamin E treatment]. Hintner H; Schuler G; Fritsch P Hautarzt; 1982 Jun; 33(6):310-4. PubMed ID: 6179897 [TBL] [Abstract][Full Text] [Related]
35. [Association of a pediatric bullous eruption, cutaneous and muscular atrophy, hyperpigmentation and dysmorphism. A new entity?]. Sciolla JP; Guillot B; Barnéon G; Montoya P; Guilhou JJ; Meynadier J Ann Dermatol Venereol; 1986; 113(4):317-27. PubMed ID: 3767229 [TBL] [Abstract][Full Text] [Related]
36. [Our experiences with congenital bullous epidermolysis in childhood]. Plachý V; Cihácek J Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove Suppl; 1973; 16(2):159-64. PubMed ID: 4528261 [No Abstract] [Full Text] [Related]
37. [The effect of collagenase inhibition on bullous eruption and healing process in epidermolysis bullosa]. Coradello H; Lubec G Hautarzt; 1979 Feb; 30(2):89-91. PubMed ID: 217851 [TBL] [Abstract][Full Text] [Related]
38. Prenatal exclusion of Herlitz syndrome by electron microscopy of fetal skin biopsies obtained at fetoscopy. Löfberg L; Anton-Lamprecht I; Michaëlsson G; Gustavii B Acta Derm Venereol; 1983; 63(3):185-9. PubMed ID: 6192629 [TBL] [Abstract][Full Text] [Related]
40. Prenatal detection of epidermolysis bullosa letalis with pyloric atresia in a fetus by abnormal ultrasound and elevated alpha-fetoprotein. Dolan CR; Smith LT; Sybert VP Am J Med Genet; 1993 Sep; 47(3):395-400. PubMed ID: 7510931 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]