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

Clinical and laboratory findings and etiologies of genetic homocystinemia: a single-center experience

20 Sept 2023

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 Alcoholism and Thiamine Deficiency
Share to Folate and B Vitamins Research
Share to Sulfur Compounds in Biology

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 37728847
DOI: 10.1007/s13760-023-02356-1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical and laboratory findings and etiologies of genetic homocystinemia: a single-center experiencePMID 37728847Read ↗

Classical homocystinuria: A common inborn error of metabolism? An epidemiological study based on genetic databasesSemantic proximity Read ↗

Varied phenotypic presentations of homocystinuria in two siblings.Semantic proximity Read ↗

Common metabolic disorder (inborn errors of metabolism) concerns in primary care practiceSemantic proximity Read ↗

Cystinuria: an update on pathophysiology, genetics, and clinical managementSemantic proximity Read ↗

Aminoacidopathies: Prevalence, Etiology, Screening, and Treatment OptionsSemantic proximity Read ↗

Cystinuria: recent advances in pathophysiology and genetics.Semantic proximity Read ↗

Homocystinuria: Challenges in diagnosis and managementSemantic proximity Read ↗

Clinical and Genetic Characteristics of 111 Children Diagnosed by Gene Testing in the Pediatric Digestive Department: A Single-Center Retrospective AnalysisSemantic proximity Read ↗

Current genetic defects in common variable immunodeficiency patients on the geography between Europe and Asia: a single-center experienceSemantic proximity Read ↗

[Clinical diagnosis of genetic liver disease].Semantic proximity Read ↗

Glucose-6-phosphate dehydrogenase deficiency: a historical perspectiveSemantic proximity Read ↗

Diagnosis and evaluation of primary panhypogammaglobulinemia: a molecular and genetic challenge.Semantic proximity Read ↗

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