References
- McLachlan, R, Grigg, AP, Cornell, FN, et al. Demonstration of monoclonal IgE by isoelectric focusing: first reported case of IgE myeloma in Australia. Clin Chem 1988; 34: 2168–2171
- McLachlan R. Isoelectric focusing of immunoglobulins. Atlas of patterns II. Clin Biochem Monogr November, 1989; 26–32
- Aziz, KE, Montanaro, A, McCluskey, PJ, et al. Sjögren's syndrome: review with recent insights into immunopathogenesis. Aust NZ J Med 1992; 22: 671–678
- Osserman EF, Takatsuki K. Clinical and immunochemical studies of four cases of heavy (Hγ2) chain disease. Am J Med 1964; 37: 351–373
- Franklin, EC, Lowenstein, J, Bigelow, B, et al. Heavy chain disease — a new disorder of serum γ-globulins: report of the first case. Am J Med 1964; 37: 332–350
- Wager, O, Räsänen, JA, Lindeberg, L, et al. Two cases of IgG heavy-chain disease. Acta Pathol Microbiol Scand 1969; 75: 350–352
- Lyons, RM, Chaplin, H, Tillack, TW, et al. Gamma heavy chain disease: rapid, sustained response to cyclophosphamide and prednisone. Blood 1975; 46: 1–9
- Fermand, J-P, Brouet, J-C, Danon, F, et al. Gamma heavy chain “disease”: heterogeneity of the clinicopathologic features. Report of 16 cases and review of the literature. Medicine (Baltimore) 1989; 68: 321–335
- Venables, PJW. Sjögren's syndrome and overlap syndromes. Oxford Textbook of Clinical Nephrology1st edn., S Cameron, Davidson, AM, Grünfeld, J-P, et al. Oxford University Press, Oxford 1992; 1: 693–699, In
- Bloch, KJ, Buchanan, WW, Wohl, MJ, et al. Sjögren's syndrome. A clinical, pathological and serological study of sixty-two cases. Medicine (Baltimore) 1965; 44: 187–231
- Talal N. Sjögren's syndrome, lymphoproliferation and renal tubular acidosis. Ann Int Med 1971; 74: 633–634
- Shirakura, T, Kobayashi, Y, Murai, Y, et al. A case of gamma heavy chain disease associated with autoimmune haemolytic anaemia: clinical, haematological, immunological and pathological details. Scand J Haematol 1976; 16: 387–393
- Kyle RA, Greipp PR, Banks PM. The diverse picture of gamma heavy-chain disease. Report of seven cases and review of the literature. Mayo Clinic Proceedings 1981; 56: 439–451