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

Age dependence of endogenous galactose formation in Q188R homozygous galactosemic patients.

Molecular genetics and metabolism - 1 Jan 2004

Schadewaldt Peter, Kamalanathan Loganathan, Hammen Hans Werner, Wendel Udo

Abstract excerpt

The age dependence of endogenous galactose formation was investigated in Q188R homozygous galactosemic patients (n=18; 4-38 years) using the primed continuous infusion approach with D-[1-13C]galactose as a substrate. Studies were conducted under postabsorptive conditions (fasting >10h) and good m...

Read the complete abstract on PubMed

Topics

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

Share to Age Factors
Share to Body Height
Share to Body Weight

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Carbon Isotopes

Share to Galactose

Share to Galactosemias

Share to Models, Biological

Share to UTP-Hexose-1-Phosphate Uridylyltransferase

Source

Identifiers

PMID: 14728989
DOI: 10.1016/j.ymgme.2003.10.007

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-14728989-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 9 closest

Age dependence of endogenous galactose formation in Q188R homozygous galactosemic patients.PMID 14728989Read ↗

Risk factors for premature ovarian failure in females with galactosemia.Semantic proximity Read ↗

Effects of temporary low-dose galactose supplements in children aged 5-12 y with classical galactosemia: a pilot study.Semantic proximity Read ↗

Urine and plasma galactitol in patients with galactose-1-phosphate uridyltransferase deficiency galactosemia.Semantic proximity Read ↗

In vivo oxidation of [13C]galactose in patients with galactose-1-phosphate uridyltransferase deficiency.Semantic proximity Read ↗

Pathways of galactose metabolism by galactosemics: evidence for galactose conversion to hepatic UDPglucose.Semantic proximity Read ↗

Biochemical and molecular studies of 132 patients with galactosemia.Semantic proximity Read ↗

Evidence for alternate galactose oxidation in a patient with deletion of the galactose-1-phosphate uridyltransferase gene.Semantic proximity Read ↗

Black children deficient in galactose 1-phosphate uridyltransferase: correlation of activity and immunoreactive protein in erythrocytes and leukocytes.Semantic proximity Read ↗

Galactose-1-phosphate uridylyltransferase: kinetics of formation and reaction of uridylyl-enzyme intermediate in wild-type and specifically mutated uridylyltransferases.Semantic proximity Read ↗

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