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

Variants of alpha 1-proteinase inhibitor in black and white South African patients with focal glomerulosclerosis and minimal change nephrotic syndrome.

Journal of medical genetics - 1 Jan 1998

Halkas A C, Gaillard M C, Thomson P D, Green S L, Ludewick H, Kala U

Abstract excerpt

OBJECTIVE: To determine the prevalence and biochemical characteristics of certain alleles of alpha 1-proteinase inhibitor in black and white South African patients with two common types of pathology causing the nephrotic syndrome. DESIGN: A cross sectional study of black and white patients with focal glomerulosclerosis (FGS) or minimal change disease (MCNS) and black and white controls. SETTING: The patients were...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to alpha 1-Antitrypsin

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Black People

Share to Child, Preschool

Share to Gene Frequency

Share to Genetic Variation

Share to White People

Source

Open in PubMed Open full text

Identifiers

PMID: 9475086
DOI: 10.1136/jmg.35.1.6
PMCID: PMC1051178

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

Variants of alpha 1-proteinase inhibitor in black and white South African patients with focal glomerulosclerosis and minimal change nephrotic syndrome.PMID 9475086Read ↗

The podocin V260E mutation predicts steroid resistant nephrotic syndrome in black South African children with focal segmental glomerulosclerosis.Semantic proximity Read ↗

Identification of DNA polymorphisms associated with the V type alpha1-antitrypsin gene.Semantic proximity Read ↗

Health implications of alpha1-antitrypsin deficiency in Sub-Sahara African countries and their emigrants in Europe and the New World.Semantic proximity Read ↗

Alpha-1-antitrypsin phenotypes in patients with renal arterial fibromuscular dysplasia.Semantic proximity Read ↗

Genetic polymorphisms of the renin-angiotensin system and the outcome of focal segmental glomerulosclerosis in children.Semantic proximity Read ↗

MCP1 2518 A/G polymorphism affects progression of childhood focal segmental glomerulosclerosis.Semantic proximity Read ↗

Familial focal segmental glomerulosclerosis (FSGS) in a Nigerian family and exclusion of mutations in NPHS2,WT1 and APOL1.Semantic proximity Read ↗

Differences in the prevalence of a TaqI RFLP in the 3' flanking region of the alpha 1-proteinase inhibitor gene between asthmatic and non-asthmatic black and white South Africans.Semantic proximity Read ↗

Functional genetic variation in aminopeptidase A (ENPEP): lack of clear association with focal and segmental glomerulosclerosis (FSGS).Semantic proximity Read ↗

Methylenetetrahydrofolate reductase polymorphism in childhood primary focal segmental glomerulosclerosis.Semantic proximity Read ↗

Secretory leukocyte proteinase inhibitor, alpha-1-antitrypsin deficiency and emphysema: Preliminary study, speculation and an hypothesis.Semantic proximity Read ↗

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