Molecular pathology of nephrotic syndrome in childhood: a contemporary approach to diagnosis (Q37156672)

18 August 2017

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title

Molecular pathology of nephrotic syndrome in childhood: a contemporary approach to diagnosis (English)

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18 August 2017

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Helen Liapis

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18 August 2017

publication date

1 July 2008

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Pediatric and Developmental Pathology

18 August 2017

published in

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18 August 2017

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18 August 2017

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18 August 2017

page(s)

154-163

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The origins and development of the concept of a "nephrotic syndrome".

18 August 2017

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High incidence of initial and late steroid resistance in childhood nephrotic syndrome

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A proposed taxonomy for the podocytopathies: a reassessment of the primary nephrotic diseases

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Cell biology of the glomerular podocyte

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Molecular basis of the functional podocin-nephrin complex: mutations in the NPHS2 gene disrupt nephrin targeting to lipid raft microdomains

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A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis

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Collapsing glomerulopathy in HIV and non-HIV patients: a clinicopathological and follow-up study

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Bone morphogenetic protein-7 delays podocyte injury due to high glucose

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Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).

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The number of podocyte slit diaphragms is decreased in minimal change nephrotic syndrome.

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Respiratory chain deficiency presenting as congenital nephrotic syndrome

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Cytomegalovirus-related congenital nephrotic syndrome with diffuse mesangial sclerosis

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Podocyte proteins in Galloway-Mowat syndrome

21 January 2018

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Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database

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Expanding the clinical spectrum of Frasier syndrome

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WT1 and PAX-2 podocyte expression in Denys-Drash syndrome and isolated diffuse mesangial sclerosis

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Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities

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Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders

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Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

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Focal and segmental glomerulosclerosis: varying biologic mechanisms underlie a final histopathologic end point

21 January 2018

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NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.

21 January 2018

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Broadening the spectrum of diseases related to podocin mutations

21 January 2018

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Expression profile of nephrin, podocin, and CD2AP in Chinese children with MCNS and IgA nephropathy

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21 January 2018

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21 January 2018

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COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement

21 January 2018

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Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency

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Gene Expression Profiles of Podocyte-Associated Molecules as Diagnostic Markers in Acquired Proteinuric Diseases

21 January 2018

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Expression of nephrin in acquired forms of nephrotic syndrome in childhood

21 January 2018

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21 January 2018

Identifiers

DOI

10.2350/07-11-0375.1

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18 August 2017

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