(Q38062343)

28 August 2017

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title

The renal biopsy in the genomic era. (English)

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28 August 2017

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Helen Liapis

1

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PubMed ID

23179194

28 August 2017

Joseph P Gaut

series ordinal

2

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28 August 2017

21 November 2012

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28 August 2017

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28 August 2017

28

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28 August 2017

8

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28 August 2017

1207-1219

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https://scigraph.springernature.com/pub.10.1007/s00467-012-2356-9

28 August 2017

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21 January 2018

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Early ultrastructural changes in renal allografts: correlation with antibody-mediated rejection and transplant glomerulopathy.

21 January 2018

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21 January 2018

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21 January 2018

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Risk factors for cyclosporine-induced tubulointerstitial lesions in children with minimal change nephrotic syndrome

21 January 2018

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Nephrotoxicity as a cause of acute kidney injury in children.

21 January 2018

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21 January 2018

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21 January 2018

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Gene expression profiling in glomeruli from human kidneys with diabetic nephropathy.

21 January 2018

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A molecular classifier for predicting future graft loss in late kidney transplant biopsies

21 January 2018

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21 January 2018

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Experimental approaches to the human renal transcriptome

21 January 2018

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Interpreting gene-expression profiles in transplantation: a critical appraisal

21 January 2018

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Expression profiles of congenital renal dysplasia reveal new insights into renal development and disease.

21 January 2018

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Characterization of heterogeneity in the molecular pathogenesis of lupus nephritis from transcriptional profiles of laser-captured glomeruli

21 January 2018

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C3 glomerulonephritis: clinicopathological findings, complement abnormalities, glomerular proteomic profile, treatment, and follow-up

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

21 January 2018

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Specific podocin mutations determine age of onset of nephrotic syndrome all the way into adult life

21 January 2018

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Patients with ACTN4 mutations demonstrate distinctive features of glomerular injury.

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome.

21 January 2018

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Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome

21 January 2018

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Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrum

21 January 2018

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C3 glomerulopathy: a new classification

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00467-012-2356-9

Membranoproliferative glomerulonephritis and C3 glomerulopathy: resolving the confusion

21 January 2018

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21 January 2018

Dense deposit disease.

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2356-9

Proliferative glomerulonephritis secondary to dysfunction of the alternative pathway of complement

21 January 2018

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Atypical hemolytic uremic syndrome in children: complement mutations and clinical characteristics

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2356-9

M-type phospholipase A2 receptor as target antigen in idiopathic membranous nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2356-9

Membranous nephropathy: recent travels and new roads ahead

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00467-012-2356-9

Mechanisms of nephronophthisis and related ciliopathies

21 January 2018

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Nephronophthisis: disease mechanisms of a ciliopathy

21 January 2018

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Phenotype and outcome in hereditary tubulointerstitial nephritis secondary to UMOD mutations

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00467-012-2356-9

Novel genetic aspects of congenital anomalies of kidney and urinary tract

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00467-012-2356-9

Clinical practice. Autosomal dominant polycystic kidney disease

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00467-012-2356-9

Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: summary statement of a first National Institutes of Health/Office of Rare Diseases conference

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2356-9

Mutations in FN1 cause glomerulopathy with fibronectin deposits.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2356-9

Phenotypic expression of primary hyperoxaluria: comparative features of types I and II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2356-9

The early introduction of percutaneous renal biopsy in Italy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2356-9

Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2356-9

Incidental healed postinfectious glomerulonephritis: a study of 1012 renal biopsy specimens examined by electron microscopy

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00467-012-2356-9

The Banff 97 working classification of renal allograft pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2356-9

Diffuse mesangial sclerosis: a congenital glomerulopathy with nephrotic syndrome.

21 January 2018

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12 December 2020

Gene expression analysis in renal biopsies

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12 December 2020

Molecular aetiology of primary hyperoxaluria type 1

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12 December 2020

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12 December 2020

Renal pathology in children with mitochondrial diseases

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12 December 2020

Actual practices in nephropathology: a survey and comparison with best practices

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12 December 2020

Alport syndrome. Molecular genetic aspects

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12 December 2020

The development of renal pathology

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12 December 2020

Genotype-phenotype correlation in X-linked Alport syndrome patients carrying missense mutations in the collagenous domain of COL4A5

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12 December 2020

An aid to the diagnosis of genetic disorders underlying adult-onset renal failure: a literature review.

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12 December 2020

Presence of autoantibodies against tubular and uveal cells in a patient with tubulointerstitial nephritis and uveitis (TINU) syndrome

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12 December 2020

Immune complex disease. I. Experimental acute and chronic glomerulonephritis

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12 December 2020

Cystic diseases of the kidney: molecular biology and genetics

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12 December 2020

Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis

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12 December 2020

Electron microscopic study of medical diseases of the kidney: update--1988.

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12 December 2020

Gaucher disease with nephrotic syndrome: response to enzyme replacement therapy

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12 December 2020

Persistent familial hematuria in children and the locus for thin basement membrane nephropathy

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12 December 2020

Familial glomerulopathy with giant fibrillar (fibronectin-positive) deposits: 15-year follow-up in a large kindred

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12 December 2020

Genotype–phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease

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12 December 2020

Electron microscopy in the diagnosis of lysosomal storage diseases.

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12 December 2020

Pathology of the kidney in cystinosis

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12 December 2020

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12 December 2020

Approach to renal biopsy

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12 December 2020

X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males.

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12 December 2020

A reevaluation of routine electron microscopy in the examination of native renal biopsies

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12 December 2020

Pierson syndrome in an adolescent girl with nephrotic range proteinuria but a normal GFR

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12 December 2020

Histopathology, ultrastructure, and clinical phenotypes in thin glomerular basement membrane disease variants

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12 December 2020

Electron microscopic investigations of the renal glomeruli

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12 December 2020

Laser capture microdissection-microarray analysis of focal segmental glomerulosclerosis glomeruli

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12 December 2020

A Mother and Daughter with Unexplained Renal Failure

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12 December 2020

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12 December 2020

APOE Kyoto mutation in European Americans with lipoprotein glomerulopathy

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12 December 2020

Acute tubulointerstitial nephritis in 21 Japanese children

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12 December 2020

Practice guidelines for the renal biopsy

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12 December 2020

Familial plasma lecithin: cholesterol acyltransferase (LCAT) deficiency. Ultrastructural aspects of a new syndrome with particular reference to lesions in the kidneys and the spleen

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12 December 2020

Familial nephropathy and multiple exostoses with exostosin-1 (EXT1) gene mutation

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12 December 2020

Congenital nephrotic syndrome in mice lacking CD2-associated protein

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12 December 2020

10.1007/S00467-012-2356-9

Identifiers

DOI

1 reference

PubMed ID

23179194

Dimensions Publication ID

28 August 2017

0 references

1 reference

PubMed ID

23179194