Association of an anatomo-pathological syndrome of male pseudohermaphroditism, Wilms' tumor, parenchymatous nephropathy and XX/XY mosaicism
about
The Denys-Drash syndromeFrasier and Denys-Drash syndromes: different disorders or part of a spectrum?Tumour suppressor gene mutations in humans and mice: parallels and contrastsHemolytic uremic syndrome as the presenting manifestation of WT1 mutation and Denys-Drash syndrome: a case report.Denys-Drash syndrome, septated vagina and low level of anti-Mullerian hormone in male neonate.Molecular genetics of Müllerian duct formation, regression and differentiationIdentification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation databaseAnalysis of wilms tumors using SNP mapping array-based comparative genomic hybridization.Renin levels in nephroblastoma (Wilms' tumour). Report of a renin secreting tumour.A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1.WT1 and PAX-2 podocyte expression in Denys-Drash syndrome and isolated diffuse mesangial sclerosis.NPHS2 mutations account for only 15% of nephrotic syndrome cases.Wilms' tumor protein Wt1 is an activator of the anti-Müllerian hormone receptor gene Amhr2.Screening of WT1 mutations in exon 8 and 9 in children with steroid resistant nephrotic syndrome from a single centre and establishment of a rapid screening assay using high-resolution melting analysis in a clinical setting.Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour.Two cases of isolated diffuse mesangial sclerosis with WT1 mutations.WT1 mutants reveal SRPK1 to be a downstream angiogenesis target by altering VEGF splicing.The World's Youngest Cadaveric Kidney Transplant: Medical, Surgical and Ethical Issues.Inactivation of Map3k7 in Foxd1-expressing cells results in loss of mesangial PDGFRβ and juvenile kidney scarring.Management of Denys-Drash syndrome: A case series based on an international survey
P2860
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P2860
Association of an anatomo-pathological syndrome of male pseudohermaphroditism, Wilms' tumor, parenchymatous nephropathy and XX/XY mosaicism
description
1967 nî lūn-bûn
@nan
1967 թուականին հրատարակուած գիտական յօդուած
@hyw
1967 թվականին հրատարակված գիտական հոդված
@hy
1967年の論文
@ja
1967年論文
@yue
1967年論文
@zh-hant
1967年論文
@zh-hk
1967年論文
@zh-mo
1967年論文
@zh-tw
1967年论文
@wuu
name
Association of an anatomo-path ...... ephropathy and XX/XY mosaicism
@ast
Association of an anatomo-path ...... ephropathy and XX/XY mosaicism
@en
Association of an anatomo-path ...... ephropathy and XX/XY mosaicism
@nl
type
label
Association of an anatomo-path ...... ephropathy and XX/XY mosaicism
@ast
Association of an anatomo-path ...... ephropathy and XX/XY mosaicism
@en
Association of an anatomo-path ...... ephropathy and XX/XY mosaicism
@nl
prefLabel
Association of an anatomo-path ...... ephropathy and XX/XY mosaicism
@ast
Association of an anatomo-path ...... ephropathy and XX/XY mosaicism
@en
Association of an anatomo-path ...... ephropathy and XX/XY mosaicism
@nl
P2093
P1476
[Association of an anatomo-pat ...... phropathy and XX/XY mosaicism]
@en
P2093
Proesmans W
Van Den Berghe H
P304
P577
1967-08-01T00:00:00Z