-
2
-
-
0021154660
-
Racial difference in the prevalence of IgA-associated nephropathies
-
Galla JH, Kohaut EC, Alexander R et al. Racial difference in the prevalence of IgA-associated nephropathies. Lancet 1984; 2: 522
-
(1984)
Lancet
, vol.2
, pp. 522
-
-
Galla, J.H.1
Kohaut, E.C.2
Alexander, R.3
-
3
-
-
0032884792
-
Familial IgA nephropathy
-
Scolari F. Familial IgA nephropathy. J Nephrol 1999; 12: 213-219
-
(1999)
J Nephrol
, vol.12
, pp. 213-219
-
-
Scolari, F.1
-
4
-
-
0027355460
-
Multiplex families in IgA nephropathy
-
Levy M. Multiplex families in IgA nephropathy. Contrib Nephrol 1993; 104: 46-53
-
(1993)
Contrib Nephrol
, vol.104
, pp. 46-53
-
-
Levy, M.1
-
5
-
-
0033762699
-
IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23
-
Gharavi AG, Yan Y, Scolari F et al. IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23. Nat Genet 2000; 26: 354-357
-
(2000)
Nat Genet
, vol.26
, pp. 354-357
-
-
Gharavi, A.G.1
Yan, Y.2
Scolari, F.3
-
6
-
-
33847663024
-
Localization of a novel disease susceptibility locus to chromosome 2q36 by genome scan of a large extended Canadian family with IgA nephropathy (IgAN)
-
Pei YPA, Magistroni R, Klassen J, Kappel J, Cattran D, St George P. Localization of a novel disease susceptibility locus to chromosome 2q36 by genome scan of a large extended Canadian family with IgA nephropathy (IgAN). J Am Soc Nephrol 2005; 16 [Suppl S]: 592A
-
(2005)
J Am Soc Nephrol
, vol.16
, Issue.SUPPL. S
-
-
Pei, Y.P.A.1
Magistroni, R.2
Klassen, J.3
Kappel, J.4
Cattran, D.5
St George, P.6
-
7
-
-
33845227377
-
Genetic heterogeneity in Italian families with IgA nephropathy: Suggestive linkage for two novel IgA nephropathy loci
-
Bisceglia L, Cerullo G, Forabosco P. et al. Genetic heterogeneity in Italian families with IgA nephropathy: Suggestive linkage for two novel IgA nephropathy loci. Am J Hum Genet 2006; 79: 1130-1134
-
(2006)
Am J Hum Genet
, vol.79
, pp. 1130-1134
-
-
Bisceglia, L.1
Cerullo, G.2
Forabosco, P.3
-
9
-
-
0034098774
-
Allegro, a new computer program for multipoint linkage analysis
-
Gudbjartsson DF, Jonasson K, Frigge ML et al. Allegro, a new computer program for multipoint linkage analysis. Nat Genet 2000; 25: 12-13
-
(2000)
Nat Genet
, vol.25
, pp. 12-13
-
-
Gudbjartsson, D.F.1
Jonasson, K.2
Frigge, M.L.3
-
10
-
-
0035984454
-
Consanguinity in a population sample of Israeli Muslim Arabs, Christian Arabs and Druze
-
Vardi-Saliternik R, Friedlander Y, Cohen T. Consanguinity in a population sample of Israeli Muslim Arabs, Christian Arabs and Druze. Ann Hum Biol 2002; 29: 422-431
-
(2002)
Ann Hum Biol
, vol.29
, pp. 422-431
-
-
Vardi-Saliternik, R.1
Friedlander, Y.2
Cohen, T.3
-
11
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander E, Kruglyak L. Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results. Nat Genet 1995; 11: 241-247
-
(1995)
Nat Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
12
-
-
0034051681
-
Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis
-
Kaplan JM, Kim SH, North KN et al. mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis. Nat Genet 2000; 24: 251-256
-
(2000)
Nat Genet
, vol.24
, pp. 251-256
-
-
Kaplan, J.M.1
Kim, S.H.2
North, K.N.3
-
13
-
-
20844461826
-
A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis
-
Winn MP, Conlon PJ, Lynn KL et al. A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis. Science 2005; 308: 1801-1804
-
(2005)
Science
, vol.308
, pp. 1801-1804
-
-
Winn, M.P.1
Conlon, P.J.2
Lynn, K.L.3
-
14
-
-
0036156915
-
Increased risk of end-stage renal disease in familial IgA nephropathy
-
Schena FP, Cerullo G, Rossini M et al. Increased risk of end-stage renal disease in familial IgA nephropathy. J Am Soc Nephrol 2002; 13: 453-460
-
(2002)
J Am Soc Nephrol
, vol.13
, pp. 453-460
-
-
Schena, F.P.1
Cerullo, G.2
Rossini, M.3
-
15
-
-
33646064092
-
IgA nephropathy: The presence of familial disease does not confer an increased risk for progression
-
Izzi C, Ravani P, Torres D et al. IgA nephropathy: The presence of familial disease does not confer an increased risk for progression. Am J Kidney Dis 2006; 47: 761-769
-
(2006)
Am J Kidney Dis
, vol.47
, pp. 761-769
-
-
Izzi, C.1
Ravani, P.2
Torres, D.3
-
16
-
-
0037248895
-
Mutations in the COL4A4 gene in thin basement membrane disease
-
Buzza M, Dagher H, Wang YY et al. Mutations in the COL4A4 gene in thin basement membrane disease. Kidney Int 2003; 63: 447-453
-
(2003)
Kidney Int
, vol.63
, pp. 447-453
-
-
Buzza, M.1
Dagher, H.2
Wang, Y.Y.3
-
17
-
-
0030900198
-
Thin GBM nephropathy: Premature glomerular obsolescence is associated with hypertension and late onset renal failure
-
Nieuwhof CM, de Heer F, de Leeuw P et al. Thin GBM nephropathy: premature glomerular obsolescence is associated with hypertension and late onset renal failure. Kidney Int 1997; 51: 1596-1601
-
(1997)
Kidney Int
, vol.51
, pp. 1596-1601
-
-
Nieuwhof, C.M.1
de Heer, F.2
de Leeuw, P.3
-
19
-
-
0037756785
-
Consanguinity-associated kidney diseases in Lebanon: An epidemiological study
-
Barbari A, Stephan A, Masri M et al. Consanguinity-associated kidney diseases in Lebanon: An epidemiological study. Mol Immunol 2003; 39: 1109-1114
-
(2003)
Mol Immunol
, vol.39
, pp. 1109-1114
-
-
Barbari, A.1
Stephan, A.2
Masri, M.3
-
20
-
-
0031897168
-
Familial Mediterranean fever clinical and genetic features in Druzes and in Iraqi Jews: A preliminary study
-
Touitou I, Ben-Chetrit E, Notarnicola C et al. Familial Mediterranean fever clinical and genetic features in Druzes and in Iraqi Jews: A preliminary study. J Rheumatol 1998; 25: 916-919
-
(1998)
J Rheumatol
, vol.25
, pp. 916-919
-
-
Touitou, I.1
Ben-Chetrit, E.2
Notarnicola, C.3
-
21
-
-
0035183256
-
The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA
-
Mandel H, Szargel R, Labay V et al. The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA. Nat Genet 2001; 29: 337-341
-
(2001)
Nat Genet
, vol.29
, pp. 337-341
-
-
Mandel, H.1
Szargel, R.2
Labay, V.3
-
22
-
-
0021964474
-
Familial IgA nephropathy. Evidence of an inherited mechanism of disease
-
Julian BA, Quiggins PA, Thompson JS et al. Familial IgA nephropathy. Evidence of an inherited mechanism of disease. N Engl J Med 1985; 312: 202-208
-
(1985)
N Engl J Med
, vol.312
, pp. 202-208
-
-
Julian, B.A.1
Quiggins, P.A.2
Thompson, J.S.3
-
24
-
-
33644853997
-
Familial aggregation of primary glomerulonephritis in an Italian population isolate: Valtrompia study
-
Izzi C, Sanna-Cherchi S, Prati E et al. Familial aggregation of primary glomerulonephritis in an Italian population isolate: Valtrompia study. Kidney Int 2006; 69: 1033-1040
-
(2006)
Kidney Int
, vol.69
, pp. 1033-1040
-
-
Izzi, C.1
Sanna-Cherchi, S.2
Prati, E.3
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