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3. [Case of familial bisalbuminemia]. Baldi A; De Vecchi G; Guariglia A; De Crescenzo A Quad Sclavo Diagn; 1973 Dec; 9(4):931-7. PubMed ID: 4802153 [No Abstract] [Full Text] [Related]
4. Bisalbuminemia from a clinical chemist's viewpoint: a case report and review of the recent literature. Faviou E; Nounopoulos C; Dionyssiou-Asteriou A Minerva Med; 2006 Jun; 97(3):287-93. PubMed ID: 16855523 [TBL] [Abstract][Full Text] [Related]
6. Bisalbuminemia: an interesting electrophoretic abnormality--a report of two cases. Thakar YS; Chande C; Dhanvijay AG; Shrikhande AV; Saoji AM Indian J Pathol Microbiol; 1997 Oct; 40(4):559-61. PubMed ID: 9444873 [TBL] [Abstract][Full Text] [Related]
7. Study of two cases of bisalbuminemia by electrofocusing. Sudaka P; Rigat AM; Masseyeff R; Liebschutz H Biomedicine; 1976 Dec; 25(9):337-41. PubMed ID: 1000041 [TBL] [Abstract][Full Text] [Related]
8. [Unusual transient M-proteinemia (IgG-kappa type) detected using separax membrane. A case report]. Nakaguchi S; Okumura J; Sasajima M; Horita H; Nagahara M; Kumatani S; Hashimoto T Rinsho Byori; 1994 Dec; 42(12):1299-302. PubMed ID: 7869596 [TBL] [Abstract][Full Text] [Related]
9. [Inherited and familial bisalbuminemia. Acquired transient bisalbuminemia (author's transl)]. Le Treut A; Catheline M; Cloarec L Pathol Biol (Paris); 1977 Jan; 25(1):45-55. PubMed ID: 322036 [TBL] [Abstract][Full Text] [Related]
11. Mutations and polymorphisms of the gene of the major human blood protein, serum albumin. Minchiotti L; Galliano M; Kragh-Hansen U; Peters T Hum Mutat; 2008 Aug; 29(8):1007-16. PubMed ID: 18459107 [TBL] [Abstract][Full Text] [Related]
13. [Study of a family with a slow type of bisalbuminemia and of 2 other familial cases]. Carniato A; Caenaro GF; Chirillo R Quad Sclavo Diagn; 1977 Jun; 13(2):176-85. PubMed ID: 594304 [TBL] [Abstract][Full Text] [Related]
14. [Hereditary bisalbuminemia. Study of a new familial case in France (author's transl)]. Beaudonnet A; Pichot J; Plauchu H; Revenant MC Ann Biol Clin (Paris); 1978; 36(1):11-7. PubMed ID: 80145 [TBL] [Abstract][Full Text] [Related]
15. Gamma heavy chain disease screening showing a discrepancy between electrophoretic and nephelometric determinations of serum gamma globulin concentration. Takatani T; Morita K; Takaoka N; Tatsumi M; Okuno Y; Masutani T; Murakawa K; Fukui A; Tsukaguchi N; Okamoto Y Ann Clin Biochem; 2002 Sep; 39(Pt 5):531-3. PubMed ID: 12227865 [TBL] [Abstract][Full Text] [Related]
17. A second albumin variant in an Irish population. Leahy DT; McLaughlin H Clin Chim Acta; 1987 Oct; 168(3):273-9. PubMed ID: 3677425 [TBL] [Abstract][Full Text] [Related]
18. [On a case of bisalbuminemia, rare genetic variation of human albumin]. Canella G; Caldera L; Marchi C Fracastoro; 1971; 64(4):242-6. PubMed ID: 5157313 [No Abstract] [Full Text] [Related]
19. Structural analysis and fatty acid-binding properties of two Croatian variants of human serum albumin. Kragh-Hansen U; Campagnoli M; Dodig S; Nielsen H; Benko B; Raos M; Cesati R; Sala A; Galliano M; Minchiotti L Clin Chim Acta; 2004 Nov; 349(1-2):105-12. PubMed ID: 15469862 [TBL] [Abstract][Full Text] [Related]
20. [A case of alloalbuminemia (familial congenital bisalbuminemia) in a subject with hepatic cirrhosis]. Mondavio M; Morino P; De Giorgis L; Ferraro G; Ghiazza GF Minerva Dietol Gastroenterol; 1986; 32(1):87-92. PubMed ID: 3703323 [No Abstract] [Full Text] [Related] [Next] [New Search]