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

Gaucher disease and β-thalassemia: A rare coinheritance.

Blood cells, molecules & diseases - 1 Jun 2017

Makis Alexandros, Tzoufi Meropi, Pappa Eleni, Kyrochristos Ioannis, Zikou Anastasia, Xydis Vasileios, Argyropoulou Maria I, Chaliasos Nikolaos

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 beta-Globins
Share to beta-Thalassemia
Share to Enzyme Replacement Therapy
Share to Gaucher Disease

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Glucosylceramidase

Share to Hepatomegaly

Share to Paternal Inheritance

Share to Splenomegaly

Source

Identifiers

PMID: 28458077
DOI: 10.1016/j.bcmd.2017.04.007

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Gaucher disease and β-thalassemia: A rare coinheritance.PMID 28458077Read ↗

Coinheritance of Gaucher disease and α-thalassemia resulting in confusion between two inherited hematologic diseases.Semantic proximity Read ↗

Type 2 gaucher disease: an expanding phenotype.Semantic proximity Read ↗

Hematologically important mutations: Gaucher disease.Semantic proximity Read ↗

Hematologically important mutations: Gaucher disease.Semantic proximity Read ↗

Hematologically important mutations: Gaucher disease.Semantic proximity Read ↗

Gaucher disease and Lupus: A rare association?Semantic proximity Read ↗

Rare in Rare: Overlapping Clinical Features in a Patient With Both Gaucher Disease Type 1 and B4GALT-CDG: Expanding the Clinical Spectrum With a Novel Pathogenic Variant.Semantic proximity Read ↗

Gaucher disease.Semantic proximity Read ↗

[Gaucher's disease: diagnosis and therapy].Semantic proximity Read ↗

High risk screening for Gaucher disease in patients with splenomegaly and/or thrombocytopenia in China: 55 cases identifiedSemantic proximity Read ↗

Coexistence of β-thalassemia and polycythemia vera.Semantic proximity Read ↗

Type IIIc Gaucher disease and acrodysostosis.Semantic proximity Read ↗

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