References
- Lofters WS, Pineo GF, Luke KH. Henoch Schonlein purpura occurring in 3 members of a family. Can Med Assoc J 1973; 109: 46–8
- De Vebre LL. Henoch Schonlein purpura in a family. Can Med Assoc J 1974; 111: 16
- Levy-Khademi F, Korman SH, Amitay Y. Henoch Schonlein purpura: simultaneous occurrence in 2 siblings. Pediatr Dermatol 2000; 17: 139–40
- Meadow SR, Scott DG. Berger disease: Henoch Schonlein syndrome without a rash. J Pediatr 1985; 106: 27–32
- Robson WL, Leung AK. Henoch Schonlein purpura. Adv Pediatr 1994; 41: 163–94
- Blankenship BE. Henoch Schonlein purpura: a review. J Tenn Med Soc 1985; 78: 615–8
- Fugger L, Tisch R, Libau R, van Ender P, Mc Devitt H. The role of human major histocompatibility complex (HLA) genes in disease. The Metabolic and Molecular Bases of Inherited Disease8th edn, C Scriver, A Beaudet, W Slu, D Valle. Medical Publishing Division, Mc Graw-Hill. 1998; 311
- Amoli MA, Thomson W, Hajeer A, Calvino M, Garcia-Porrua C, Ollier W, Gonzalez-Gay M. HLA DRB1*01 association with HSP in patients from northwest Spain. J Rheumatol 2001; 28: 1266–70
- Amoroso A, Berrino M, Canale L, Coppo R, Cornaglia M, Guarrera S, Mazzola G. Immunogenetics of Henoch Schonlein disease. Eur J Immunogenet 1997; 24: 323–33