(Q33828986)

29 July 2017

Is collapsing C1q nephropathy another MYH9-associated kidney disease? A case report (English)

1 reference

29 July 2017

1 reference

1 reference

7

Carl D Langefeld

1 reference

29 July 2017

8

Barry I Freedman

1 reference

29 July 2017

3

Donald W Bowden

1 reference

29 July 2017

6

Mary E Comeau

1 reference

29 July 2017

5

Pamela J Hicks

1 reference

29 July 2017

4

Meredith A Bostrom

1 reference

PubMed ID

20116156

29 July 2017

Amber M Reeves-Daniel

series ordinal

1

object named as

Amber M Reeves-Daniel

1 reference

29 July 2017

2

Samy S Iskandar

1 reference

29 July 2017

29 January 2010

1 reference

American Journal of Kidney Diseases

29 July 2017

1 reference

29 July 2017

55

1 reference

29 July 2017

e21-4

1 reference

29 July 2017

5

1 reference

Megakaryocytes of patients with MYH9-related thrombocytopenia present an altered proplatelet formation

29 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864358

Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864358

Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864358

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864358

MYH9 is associated with nondiabetic end-stage renal disease in African Americans

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864358

A new multipoint method for genome-wide association studies by imputation of genotypes

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864358

C1q nephropathy: a variant of focal segmental glomerulosclerosis.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864358

Collapsing glomerulopathy

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864358

Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864358

Idiopathic collapsing focal segmental glomerulosclerosis: a clinicopathologic study

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864358

C1q nephropathy: a distinct pathologic entity usually causing nephrotic syndrome.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864358

C1q nephropathy: a pediatric clinicopathologic study.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864358

Genome-wide linkage analysis of serum creatinine in three isolated European populations.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864358

10.1053/J.AJKD.2009.10.060

29 October 2018

Identifiers

DOI

1 reference

29 July 2017

1 reference

29 July 2017

1 reference

PubMed ID

20116156