| Nome |
# |
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Genome-wide association study identifies susceptibility loci for IgA nephropathy, file ddc633e2-affc-4e2e-e053-3705fe0a4c80
|
690
|
|
Genomic Mismatch at LIMS1 Locus and Kidney Allograft Rejection., file ddc633e3-c884-4e2e-e053-3705fe0a4c80
|
544
|
|
IgA nephropathy, the most common cause of
glomerulonephritis, is linked to 6q22–23, file ddc633e2-a7b2-4e2e-e053-3705fe0a4c80
|
519
|
|
CHOLESTEROL CRYSTAL EMBOLISM: A RECOGNIZABLE CAUSE OF RENAL DISEASE, file ddc633e2-a7b3-4e2e-e053-3705fe0a4c80
|
515
|
|
IgA nephropathy: the presence of familial disease does not confer an increased risk for progression, file ddc633e2-a7ae-4e2e-e053-3705fe0a4c80
|
401
|
|
Uromodulin storage diseases: clinical aspects and mechanisms., file ddc633e2-a7b4-4e2e-e053-3705fe0a4c80
|
352
|
|
Cyclosporine in patients with steroid-resistant nephrotic syndrome: an open-label, nonrandomized, retrospective study, file ddc633e2-a991-4e2e-e053-3705fe0a4c80
|
348
|
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Genetic drivers of kidney defects in the digeorge syndrome, file ddc633e3-560f-4e2e-e053-3705fe0a4c80
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318
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|
Infertility and hypergonadotropic hypogonadism as first evidence of hereditary apolipoprotein A-I amyloidosis, file ddc633e2-a86b-4e2e-e053-3705fe0a4c80
|
311
|
|
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics., file ddc633e2-a7b5-4e2e-e053-3705fe0a4c80
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267
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|
Renal outcome in patients with congenital anomalies of the kidney and urinary tract., file ddc633e2-b09c-4e2e-e053-3705fe0a4c80
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238
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Defective intracellular trafficking of uromodulin mutant isoforms, file ddc633e2-a87e-4e2e-e053-3705fe0a4c80
|
235
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|
Low cerebrovascular event rate in subjects with patent foramen ovale and different clinical presentations: results from a prospective non randomized study on a population including patients with and without patent foramen ovale closure., file ddc633e3-f03f-4e2e-e053-3705fe0a4c80
|
222
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Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome., file ddc633e2-aff9-4e2e-e053-3705fe0a4c80
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214
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|
The importance of skin biopsy in the diverse clinical manifestations of cholesterol embolism., file ddc633e2-aa51-4e2e-e053-3705fe0a4c80
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188
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Repetitive fragmentation products of albumin and alpha1-antitrypsin in glomerular diseases associated with nephrotic syndrome., file ddc633e2-a86c-4e2e-e053-3705fe0a4c80
|
180
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|
Atheroembolic renal disease, file ddc633e2-b05e-4e2e-e053-3705fe0a4c80
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178
|
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Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations., file ddc633e2-b060-4e2e-e053-3705fe0a4c80
|
174
|
|
Active focal segmental glomerulosclerosis is associated with massive oxidation of plasma albumin, file ddc633e2-a87f-4e2e-e053-3705fe0a4c80
|
167
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Rituximab in Children with Steroid-Dependent Nephrotic Syndrome: A Multicenter, Open-Label, Noninferiority, Randomized Controlled Trial., file ddc633e3-cf0e-4e2e-e053-3705fe0a4c80
|
166
|
|
Coexistence of Different Circulating Anti-PodocyteAntibodies in Membranous Nephropathy, file ddc633e2-b2d1-4e2e-e053-3705fe0a4c80
|
164
|
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PREDICTORS OF RENAL AND PATIENT OUTCOMES IN ATHEROEMBOLIC RENAL DISEASE: A PROSPECTIVE STUDY., file ddc633e2-a7bd-4e2e-e053-3705fe0a4c80
|
163
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The Case | Cystic renal disease, nephrogenic diabetes insipidus, and polycytemia., file ddc633e3-ce66-4e2e-e053-3705fe0a4c80
|
163
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The pathophysiology of IgA nephropathy, file ddc633e2-bb0f-4e2e-e053-3705fe0a4c80
|
162
|
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Suprarenal aortic cross-clamping in the elective surgery of abdominal aortic aneurysms. Lessons from 68 cases out of consecutive survey of 746 abdominal aortic substitutions., file ddc633e3-33de-4e2e-e053-3705fe0a4c80
|
148
|
|
Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33., file ddc633e2-a86a-4e2e-e053-3705fe0a4c80
|
147
|
|
Renal apolipoprotein A-I amyloidosis: a rare and usually ignored cause of hereditary tubulointerstitial nephritis, file ddc633e2-b0a3-4e2e-e053-3705fe0a4c80
|
138
|
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IgA nephropathy--the case for a genetic basis becomes stronger., file ddc633e2-b09b-4e2e-e053-3705fe0a4c80
|
135
|
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Autosomal Dominant tubulointerstitial Kidney Disease with Adult onset due to a novel Renin Mutation Mapping in the Mature protein, file ddc633e3-f2d9-4e2e-e053-3705fe0a4c80
|
134
|
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Cis and trans regulatory elements in NPHS2 promoter: implications in proteinuria and progression of renal diseases, file ddc633e2-a880-4e2e-e053-3705fe0a4c80
|
133
|
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The rediscovery of uromodulin (Tamm-Horsfall protein): from tubulointerstitial nephropathy to chronic kidney disease., file ddc633e2-affa-4e2e-e053-3705fe0a4c80
|
133
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Search for genetic association between IgA nephropathy and candidate genes selected by function or by gene mapping at loci IGAN2 and IGAN3, file ddc633e2-bb7c-4e2e-e053-3705fe0a4c80
|
130
|
|
Deciphering Variability of PKD1 and PKD2 in an Italian Cohort of 643 Patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD), file ddc633e3-5611-4e2e-e053-3705fe0a4c80
|
127
|
|
Genetic approaches to human renal agenesis/hypoplasia and dysplasia., file ddc633e2-a7ac-4e2e-e053-3705fe0a4c80
|
125
|
|
GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway, file ddc633e3-55c9-4e2e-e053-3705fe0a4c80
|
124
|
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A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13., file ddc633e2-b05f-4e2e-e053-3705fe0a4c80
|
119
|
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Phenotypic expansion of DGKE-associated diseases., file ddc633e3-ce5c-4e2e-e053-3705fe0a4c80
|
115
|
|
Urinary secretion and extracellular aggregation of mutant uromodulin isoforms, file ddc633e2-b111-4e2e-e053-3705fe0a4c80
|
114
|
|
Familial aggregation of primary glomerulonephritis in an Italian population isolate: Valtrompia study, file ddc633e2-a7ad-4e2e-e053-3705fe0a4c80
|
112
|
|
Lack of association between dialysis modality and outcomes in atheroembolic renal disease, file ddc633e2-b09a-4e2e-e053-3705fe0a4c80
|
112
|
|
Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci., file ddc633e2-a87d-4e2e-e053-3705fe0a4c80
|
111
|
|
Genetic studies of IgA nephropathy: past, present, and future., file ddc633e2-b05c-4e2e-e053-3705fe0a4c80
|
111
|
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Copy number disorders are a Common Cause of Congenital Kidney Malformations, file ddc633e3-cf0f-4e2e-e053-3705fe0a4c80
|
108
|
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Mutations in DSTYK and dominant urinary tract malformations., file ddc633e2-b7e6-4e2e-e053-3705fe0a4c80
|
107
|
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Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens, file ddc633e3-cf0d-4e2e-e053-3705fe0a4c80
|
106
|
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Non-collagen genes role in digenic Alport syndrome, file ddc633e3-d25d-4e2e-e053-3705fe0a4c80
|
104
|
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The progression from obesity to type 2 diabetes in Alström syndrome., file ddc633e3-f252-4e2e-e053-3705fe0a4c80
|
103
|
|
Glomerular Autoimmune Multicomponents of Human Lupus Nephritis In Vivo (2): Planted Antigens., file ddc633e3-cf0c-4e2e-e053-3705fe0a4c80
|
101
|
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The Case ∣ Familial occurrence of retinitis pigmentosa, deafness, and nephropathy., file ddc633e2-b00d-4e2e-e053-3705fe0a4c80
|
94
|
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Glomerular autoimmune multicomponents of human lupus nephritis in vivo: α-enolase and annexin AI, file ddc633e3-d57c-4e2e-e053-3705fe0a4c80
|
91
|
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The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis, file ddc633e4-26c3-4e2e-e053-3705fe0a4c80
|
83
|
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Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds, file ddc633e2-b0a0-4e2e-e053-3705fe0a4c80
|
67
|
|
Multi-Autoantibody Signature and Clinical Outcome in Membranous Nephropathy, file ddc633e4-26c6-4e2e-e053-3705fe0a4c80
|
61
|
|
Liver biopsy discloses a new apolipoprotein A-I hereditary amyloidosis in several unrelated Italian families, file ddc633e2-b0a1-4e2e-e053-3705fe0a4c80
|
52
|
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Autoimmunity in membranous nephropathy targets aldose reductase and SOD2, file ddc633e2-b099-4e2e-e053-3705fe0a4c80
|
51
|
|
Type IV Collagen Mutations in Familial IgA Nephropathy, file ddc633e4-26c8-4e2e-e053-3705fe0a4c80
|
51
|
|
Uromodulin: from monogenic to multifactorial diseases., file ddc633e3-d120-4e2e-e053-3705fe0a4c80
|
44
|
|
Rituximab is a safe and effective long-term treatment for children with steroid and calcineurin inhibitor-dependent idiopathic nephrotic syndrome., file ddc633e3-04ef-4e2e-e053-3705fe0a4c80
|
37
|
|
Glomerular clusterin is associated with PKC-alpha/beta regulation and good outcome of membranous glomerulonephritis in humans, file ddc633e2-a7b1-4e2e-e053-3705fe0a4c80
|
36
|
|
A model to predict disease progression in patients with autosomal dominant polycystic kidney disease (ADPKD): the ADPKD Outcomes Model, file ddc633e3-ce51-4e2e-e053-3705fe0a4c80
|
33
|
|
Berger's Disease, file ddc633e2-bcea-4e2e-e053-3705fe0a4c80
|
32
|
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ORO-FACIO-DIGITAL SYNDROME, file ddc633e2-bce8-4e2e-e053-3705fe0a4c80
|
31
|
|
IDENTIFICATION OF A NEW LOCUS FOR MEDULLARY CYSTIC DISEASE ON CHROMOSOME 16, file ddc633e3-d749-4e2e-e053-3705fe0a4c80
|
26
|
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AUTOSOMAL DOMINANT MEDULLARY CYSTIC KIDNEY DISEASE, file ddc633e2-bce9-4e2e-e053-3705fe0a4c80
|
21
|
|
LES FORMES FAMILIALES DE NÉPHROPATHIE À IgA
ÉTUDES CLINIQUE ET GÉNÉTIQUE, file ddc633e2-b3c6-4e2e-e053-3705fe0a4c80
|
19
|
|
Rituximab versus steroids and cyclophosphamide for the treatment of primary membranous nephropathy: Protocol of a pilot randomised controlled trial, file ddc633e4-200c-4e2e-e053-3705fe0a4c80
|
18
|
|
Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis, file ddc633e2-b273-4e2e-e053-3705fe0a4c80
|
2
|
|
Rituximab in children with resistant idiopathic nephrotic syndrome, file ddc633e2-bb0e-4e2e-e053-3705fe0a4c80
|
1
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| Totale |
10.626 |