These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
34. [Epidermolysis bullosa hereditaria dystrophica with severe mutilations in two girls]. Balabanow K; Kapniloff S Hautarzt; 1971 Oct; 22(10):450-2. PubMed ID: 5122286 [No Abstract] [Full Text] [Related]
35. [Inherited epidermolysis bullosa: from diagnosis to reality]. Hernández-Martín A; Torrelo A Actas Dermosifiliogr; 2010 Jul; 101(6):495-505. PubMed ID: 20738968 [TBL] [Abstract][Full Text] [Related]
36. A comprehensive next-generation sequencing assay for the diagnosis of epidermolysis bullosa. Lucky AW; Dagaonkar N; Lammers K; Husami A; Kissell D; Zhang K Pediatr Dermatol; 2018 Mar; 35(2):188-197. PubMed ID: 29334134 [TBL] [Abstract][Full Text] [Related]
37. Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa. A consensus report by the Subcommittee on Diagnosis and Classification of the National Epidermolysis Bullosa Registry. Fine JD; Bauer EA; Briggaman RA; Carter DM; Eady RA; Esterly NB; Holbrook KA; Hurwitz S; Johnson L; Lin A J Am Acad Dermatol; 1991 Jan; 24(1):119-35. PubMed ID: 1999509 [TBL] [Abstract][Full Text] [Related]
38. [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]
40. Esophagitis and almost complete esophageal occlusion in a girl with epidermolysis bullosa. Djurić Z; Nagorni A; Zivanović D Turk J Pediatr; 2012; 54(3):301-4. PubMed ID: 23094544 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]