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Results:
1-7
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Results: 7
Authors:
Fuchshuber, A
Gribouval, O
Ronner, V
Kroiss, S
Karle, S
Brandis, M
Hildebrandt, F
Citation: A. Fuchshuber et al., Clinical and genetic evaluation of familial steroid-responsive nephrotic syndrome in childhood, J AM S NEPH, 12(2), 2001, pp. 374-378
Authors:
Dahan, K
Fuchshuber, A
Adamis, S
Smaers, M
Kroiss, S
Loute, G
Cosyns, JP
Hildebrandt, F
Verellen-Dumoulin, C
Pirson, Y
Citation: K. Dahan et al., Familial juvenile hyperuricemic nephropathy and autosomal dominant medullary cystic kidney disease type 2: Two facets of the same disease?, J AM S NEPH, 12(11), 2001, pp. 2348-2357
Authors:
Fuchshuber, A
Kroiss, S
Karle, S
Berthold, S
Huck, K
Burton, C
Rahman, N
Koptides, M
Deltas, C
Otto, E
Ruschendorf, F
Feest, T
Hildebrandt, F
Citation: A. Fuchshuber et al., Refinement of the gene locus for autosomal dominant medullary cystic kidney disease type 1 (MCKD1) and construction of a physical and partial transcriptional map of the region, GENOMICS, 72(3), 2001, pp. 278-284
Authors:
Back, E
Toder, R
Fuchshuber, A
Citation: E. Back et al., De novo inverted duplication of chromosome 7(q21.3 -> q35): cytogenetic diagnosis confirmed by FISH analysis, CLIN GENET, 60(1), 2001, pp. 77-82
Authors:
Boute, N
Gribouval, O
Roselli, S
Benessy, F
Lee, H
Fuchshuber, A
Dahan, K
Gubler, MC
Niaudet, P
Antignac, C
Citation: N. Boute et al., NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome, NAT GENET, 24(4), 2000, pp. 349-354
Authors:
Kroiss, S
Huck, K
Berthold, S
Ruschendorf, F
Scolari, F
Caridi, G
Ghiggeri, GM
Hildebrant, F
Fuchshuber, A
Citation: S. Kroiss et al., Evidence of further genetic heterogeneity in autosomal dominant medullary cystic kidney disease, NEPH DIAL T, 15(6), 2000, pp. 818-821
Authors:
Fuchshuber, A
Mehls, O
Citation: A. Fuchshuber et O. Mehls, Familial steroid-resistant nephrotic syndromes: recent advances, NEPH DIAL T, 15(12), 2000, pp. 1897-1900
Risultati:
1-7
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