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

[Sandhoff disease (beta-hexosaminidase alpha-chain deficiency)].

Ryoikibetsu shokogun shirizu - 1 Jan 1998

Taniike M, Okada S

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-N-Acetylhexosaminidases
Share to Diagnosis, Differential
Share to Mutation
Share to Prognosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Sandhoff Disease

Source

Identifiers

PMID: 9645091

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Sandhoff disease (beta-hexosaminidase alpha-chain deficiency)].PMID 9645091Read ↗

[Tay-Sachs disease (beta-hexosaminidase alpha-chain deficiency)].Semantic proximity Read ↗

[Lysosome disease--Sandhoff disease].Semantic proximity Read ↗

Studies in Tay-Sachs and Sandhoff's diseases. Immunologic and structural properties of hexosaminidase A and hexosaminidase B.Semantic proximity Read ↗

A novel mutation in the beta-hexosaminidase beta-subunit gene in a 14-month-old Korean boy with Sandhoff disease: first reported Korean case.Semantic proximity Read ↗

[Spinal muscular atrophy: a hexosaminidase A deficiency phenotype].Semantic proximity Read ↗

[Mucopolysaccharidosis type I (Hurler syndrome, Scheie syndrome)].Semantic proximity Read ↗

[Mucopolysaccharidosis type II (Hunter syndrome)].Semantic proximity Read ↗

[Adult Sandhoff disease presented as a motor neuron disease phenotype with slow progression].Semantic proximity Read ↗

[Clinical and molecular characteristics of a child with juvenile Sandhoff disease].Semantic proximity Read ↗

Crystallographic structure of human beta-hexosaminidase A: interpretation of Tay-Sachs mutations and loss of GM2 ganglioside hydrolysis.Semantic proximity Read ↗

Pharmacological enhancement of beta-hexosaminidase activity in fibroblasts from adult Tay-Sachs and Sandhoff Patients.Semantic proximity Read ↗

The X-ray crystal structure of human beta-hexosaminidase B provides new insights into Sandhoff disease.Semantic proximity Read ↗

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