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

Homocystinuria due to 5,10‐methylenetetra‐hydrofolate reductase deficiency revealed by stroke in adult siblings

1 Aug 1991

Abstract excerpt

Three patients from a single family of six siblings had homocystinemia and homocystinuria due to 5,10-methylenetetrahydrofolate reductase deficiency and had severe recurrent strokes in adult life. Two of the patients died 1 year after clinical onset.

Read the complete abstract on PubMed

Topics

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

Share to Amino Acid Enzymes and Metabolism
Share to Folate and B Vitamins Research
Share to Metabolism and Genetic Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 1866027
DOI: 10.1212/wnl.41.8.1313

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Homocystinuria due to 5,10‐methylenetetra‐hydrofolate reductase deficiency revealed by stroke in adult siblingsPMID 1866027Read ↗

Severe methylenetetrahydrofolate reductase deficiency revealed by a pulmonary embolism in a young adult.Semantic proximity Read ↗

Manifestations of neurological symptoms and thromboembolism in adults with MTHFR-deficiency.Semantic proximity Read ↗

Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke.Semantic proximity Read ↗

Monogenic Causes of Strokes.Semantic proximity Read ↗

Methylene tetrahydrofolate reductase mutation and stroke in a monozygotic twin.Semantic proximity Read ↗

Severe Methylenetetrahydrofolate Reductase DeficiencySemantic proximity Read ↗

Life-threatening methylenetetrahydrofolate reductase (MTHFR) deficiency with extremely early onset: characterization of two novel mutations in compound heterozygous patients.Semantic proximity Read ↗

Adult-onset severe methylenetetrahydrofolate reductase deficiency characterized by reversible spastic paraplegia with a novel mutation.Semantic proximity Read ↗

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