72 related articles for article (PubMed ID: 9561483)
21. Major histocompatibility complex haplotypes in Spanish immunoglobulin A deficiency patients: a comparative fine mapping microsatellite study.
Gual L; Martínez A; Fernández-Arquero M; García-Rodríguez MC; Ferreira A; Fontán G; de la Concha EG; Urcelay E
Tissue Antigens; 2004 Dec; 64(6):671-7. PubMed ID: 15546340
[TBL] [Abstract][Full Text] [Related]
22. HLA class II DR and DQ genotypes and haplotypes associated with rheumatic fever among a clinically homogeneous patient population of Latvian children.
Stanevicha V; Eglite J; Zavadska D; Sochnevs A; Shantere R; Gardovska D
Arthritis Res Ther; 2007; 9(3):R58. PubMed ID: 17559688
[TBL] [Abstract][Full Text] [Related]
23. Four mutations (three novel, one founder) in TACSTD2 among Iranian GDLD patients.
Alavi A; Elahi E; Tehrani MH; Amoli FA; Javadi MA; Rafati N; Chiani M; Banihosseini SS; Bayat B; Kalhor R; Amini SS
Invest Ophthalmol Vis Sci; 2007 Oct; 48(10):4490-7. PubMed ID: 17898270
[TBL] [Abstract][Full Text] [Related]
24. [Polymorphism of the microsatellites and tumor necrosis factor genes in chronic inflammatory bowel diseases].
Heresbach D; Ababou A; Bourienne A; Alizadeh M; Quelvennec E; Pagenault M; Dabadie A; Berre NH; Campion JP; Launois B; Gosselin M; Genetet B; Bretagne JF; Semana G
Gastroenterol Clin Biol; 1997; 21(8-9):555-61. PubMed ID: 9587492
[TBL] [Abstract][Full Text] [Related]
25. A study of HLA-G polymorphism and linkage disequilibrium in renal transplant patients and their donors.
Pirri A; Contieri FC; Benvenutti R; Bicalho Mda G
Transpl Immunol; 2009 Jan; 20(3):143-9. PubMed ID: 18926911
[TBL] [Abstract][Full Text] [Related]
26. Familial idiopathic membranous glomerulonephritis.
Vasmant D; Murnaghan K; Bensman A; Muller JY; Mougenot B
Int J Pediatr Nephrol; 1984 Dec; 5(4):193-6. PubMed ID: 6597809
[TBL] [Abstract][Full Text] [Related]
27. HLA non-class II genes may confer type I diabetes susceptibility in a Mapuche (Amerindian) affected family.
Pérez-Bravo F; Martinez-Laso J; Martin-Villa JM; Moscoso J; Moreno A; Serrano-Vela JI; Zamora J; Asenjo S; Gleisner A; Arnaiz-Villena A
Eur J Med Genet; 2006; 49(1):37-41. PubMed ID: 16473308
[TBL] [Abstract][Full Text] [Related]
28. Transient appearance of the lupus anticoagulant in three family members sharing the A11B35DR4 haplotype.
Bussel J; Miller S; Hilgartner M; O'Reilly R; Kempin S; Pollack M; Miller D
Am J Pediatr Hematol Oncol; 1983; 5(3):275-8. PubMed ID: 6414325
[TBL] [Abstract][Full Text] [Related]
29. The study of the extended haplotypes of rare HLA-B*2730 allele using microsatellite loci.
Grubić Z; Stingl K; Kerhin-Brkljacić V; Zunec R
Tissue Antigens; 2008 Jun; 71(6):514-9. PubMed ID: 18380778
[TBL] [Abstract][Full Text] [Related]
30. Idiopathic membranous nephropathy in two siblings.
Maccario M; Segagni S; Efficace E; Piazza V; Poggio F; Villa G; Picardi L; Bovio G; Galli F; Nai M
Nephrol Dial Transplant; 1995; 10(1):108-10. PubMed ID: 7724003
[No Abstract] [Full Text] [Related]
31. Membranous nephropathy in two human leukocyte antigen-identical brothers.
Elshihabi I; Kaye CI; Brzowski A
J Pediatr; 1993 Dec; 123(6):940-2. PubMed ID: 8229527
[TBL] [Abstract][Full Text] [Related]
32. Idiopathic membranous nephropathy in 2 twin brothers.
Vangelista A; Tazzari R; Bonomini V
Nephron; 1988; 50(1):79-80. PubMed ID: 3173611
[No Abstract] [Full Text] [Related]
33. Membranous nephropathy with anti-tubular basement membrane antibody may be X-linked.
Tay AH; Ren EC; Murugasu B; Sim SK; Tan PH; Cohen AH; Yap HK
Pediatr Nephrol; 2000 Aug; 14(8-9):747-53. PubMed ID: 10955919
[TBL] [Abstract][Full Text] [Related]
34. Idiopathic membranous nephropathy, associated with HLA-DRw3 and not related to monocyte-phagocyte system Fc receptor dysfunction, in father and son.
Mezzano S; Rojas G; Ardiles L; Caorsi I; Bertoglio JC; Lopez MI; Kunick M; Elgueta S
Nephron; 1991; 58(3):320-4. PubMed ID: 1896097
[TBL] [Abstract][Full Text] [Related]
35. Genetic factors in the outcome of idiopathic membranous nephropathy.
Zucchelli P; Ponticelli C; Cagnoli L; Aroldi A; Tabacchi P
Nephrol Dial Transplant; 1987; 1(4):265-6. PubMed ID: 3110688
[No Abstract] [Full Text] [Related]
36. Familial IgM mesangial nephropathy: a morphologic and immunogenetic study of three pedigrees.
Scolari F; Scaini P; Savoldi S; Prati E; Sacchi G; Amoroso A; Mazzola G; Canale L; Borelli I; Cristinelli L
Am J Nephrol; 1990; 10(4):261-8. PubMed ID: 2240052
[TBL] [Abstract][Full Text] [Related]
37. Familial occurrence of primary glomerulonephritis: evidence for a role of genetic factors.
Scolari F; Amoroso A; Savoldi S; Prati E; Scaini P; Manganoni A; Borelli I; Mazzola G; Canale L; Sacchi G
Nephrol Dial Transplant; 1992; 7(7):587-96. PubMed ID: 1323067
[TBL] [Abstract][Full Text] [Related]
38. Familial clustering of IgA nephropathy: further evidence in an Italian population.
Scolari F; Amoroso A; Savoldi S; Mazzola G; Prati E; Valzorio B; Viola BF; Nicola B; Movilli E; Sandrini M; Campanini M; Maiorca R
Am J Kidney Dis; 1999 May; 33(5):857-65. PubMed ID: 10213640
[TBL] [Abstract][Full Text] [Related]
39. Gene polymorphism and risk of idiopathic membranous nephropathy.
Liu D; Zhang J; Shi Y; Liu Z
Life Sci; 2019 Jul; 229():124-131. PubMed ID: 31075233
[TBL] [Abstract][Full Text] [Related]
40. Idiopathic membranous nephropathy in two brothers.
Sato K; Oguchi H; Hora K; Furukawa T; Furuta S; Shigematsu H; Yoshizawa S
Nephron; 1987; 46(2):174-8. PubMed ID: 3299123
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]