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

Conversion of PYP/HMDP scanning on sequential imaging in a patient with a TTR gene mutation.

Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology - 1 Jul 2024

Hansen Christopher L, Farber John, Binder Adam, Reist Kirk, Brailovsky Yevgeniy

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Amyloid Neuropathies, Familial
Share to TTR gene
Share to Mutation
Share to Prealbumin

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Radiopharmaceuticals

Source

Identifiers

PMID: 38216412
DOI: 10.1016/j.nuclcard.2023.101780

Genes

TTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Conversion of PYP/HMDP scanning on sequential imaging in a patient with a TTR gene mutation.PMID 38216412Read ↗

Severe progressive brain involvement in a patient with TRMT10C mutation.Semantic proximity Read ↗

Erdheim-Chester disease: The power of nuclear medicine imaging.Semantic proximity Read ↗

Nuclear medicine and molecular imaging advances in the 21st centurySemantic proximity Read ↗

Abnormal myocardial scintigraphy in a GTP cyclohydrolase 1 mutation carrier with Parkinson's disease.Semantic proximity Read ↗

Functional imaging in PNH caused by a new FilaminA mutation.Semantic proximity Read ↗

An unusual DMSA scan: answer.Semantic proximity Read ↗

Teaching NeuroImages: Subacute encephalopathy in a young woman with THTR2 gene mutation.Semantic proximity Read ↗

Tc-99m PYP scintigraphy identified multi-organ disease associated with transthyretin Phe64Ser mutation.Semantic proximity Read ↗

REMOVAL: Pelvic MRI in a 17-year-old XY girl with 5-alpha reductase deficiency and a homozygous Gly115Asp mutation in SRD5A2.Semantic proximity Read ↗

Transthyretin Amyloid Cardiomyopathy Diagnosed on Incidental Myocardial Uptake During Bone Scintigraphy.Semantic proximity Read ↗

Teaching Video NeuroImage: TWNK Mutation Causes Chronic Progressive External Ophthalmoplegia and Cerebellar Ataxia: A POLG-Like Phenotype.Semantic proximity Read ↗

A distinct imaging phenotype in amyotrophic lateral sclerosis confidently detected on T1 MTC.Semantic proximity Read ↗

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