Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Is collapsing C1q nephropathy another MYH9-associated kidney disease? A case report.

American journal of kidney diseases : the official journal of the National Kidney Foundation - 1 May 2010

Reeves-Daniel Amber M, Iskandar Samy S, Bowden Donald W, Bostrom Meredith A, Hicks Pamela J, Comeau Mary E, Langefeld Carl D, Freedman Barry I

Abstract excerpt

C1q nephropathy is a rare kidney disease that can present with nephrotic syndrome and typically has the histologic phenotype of either minimal change disease or focal segmental glomerulosclerosis (FSGS). Disagreement exists about whether it is a distinct immune complex-mediated glomerulopathy or...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Complement C1q
Share to Glomerulosclerosis, Focal Segmental

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Kidney Failure, Chronic

Share to Kidney Glomerulus

Share to Kidney Tubules

Share to Molecular Motor Proteins

Share to Myosin Heavy Chains

Share to Nephrotic Syndrome

Source

Open in PubMed Open full text

Identifiers

PMID: 20116156
DOI: 10.1053/j.ajkd.2009.10.060
PMCID: PMC2864358

Genes

MYH9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20116156-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Is collapsing C1q nephropathy another MYH9-associated kidney disease? A case report.PMID 20116156Read ↗

Coincident idiopathic focal segmental glomerulosclerosis collapsing variant and diabetic nephropathy in an African American homozygous for MYH9 risk variants.Semantic proximity Read ↗

The spectrum of MYH9-associated nephropathy.Semantic proximity Read ↗

Genetics of Focal Segmental Glomerulosclerosis and Human Immunodeficiency Virus–Associated Collapsing Glomerulopathy: The Role of MYH9 Genetic VariationSemantic proximity Read ↗

Idiopathic collapsing glomerulopathy is associated with APOL1 high-risk genotypes or Mendelian variants in most affected individuals in a highly admixed population.Semantic proximity Read ↗

CKD in MYH9-related disorders.Semantic proximity Read ↗

Patients with Epstein-Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease.Semantic proximity Read ↗

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

Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study.Semantic proximity Read ↗

AKI and Collapsing Glomerulopathy Associated with COVID-19 and APOL 1 High-Risk Genotype.Semantic proximity Read ↗

The non-muscle Myosin heavy chain 9 gene (MYH9) is not associated with lupus nephritis in African Americans.Semantic proximity Read ↗

Collapsing glomerulopathy in a young woman with APOL1 risk alleles following acute parvovirus B19 infection: a case report investigation.Semantic proximity Read ↗

MYH9 genetic variants associated with glomerular disease: what is the role for genetic testing?Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.