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

Maternally inherited diabetes and deafness with cerebellar ataxia: a new clinical phenotype associated with the mitochondrial DNA 3243 mutation.

Journal of neurology - 1 Jul 1997

Arai M, Ohshima 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 Brain
Share to Cerebellar Ataxia
Share to Deafness
Share to Diabetes Mellitus, Type 2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA, Mitochondrial

Share to Magnetic Resonance Imaging

Share to Mutation

Source

Identifiers

PMID: 9266470
DOI: 10.1007/s004150050126

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

Maternally inherited diabetes and deafness with cerebellar ataxia: a new clinical phenotype associated with the mitochondrial DNA 3243 mutation.PMID 9266470Read ↗

Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation.Semantic proximity Read ↗

Clinical Characteristics of Diabetes in People with Mitochondrial DNA 3243A>G Mutation in Korea.Semantic proximity Read ↗

Identification of m.3243A>G mitochondrial DNA mutation in patients with cerebellar ataxia.Semantic proximity Read ↗

Diabetes Associated With Maternally Inherited Diabetes and Deafness (MIDD): From Pathogenic Variant to Phenotype.Semantic proximity Read ↗

Maternally inherited diabetes and deafness (MIDD): unusual occult exocrine pancreatic manifestation in an affected German family.Semantic proximity Read ↗

The Mutations and Clinical Variability in Maternally Inherited Diabetes and Deafness: An Analysis of 161 Patients.Semantic proximity Read ↗

Screening for Maternally Inherited Diabetes and Deafness in Large Cohorts of Hearing Impaired and Diabetic Patients.Semantic proximity Read ↗

Two sisters with macular dystrophy caused by the 3243A>G mitochondrial DNA mutation.Semantic proximity Read ↗

Diagnosis of maternally inherited diabetes and deafness (mitochondrial A3243G mutation) based on funduscopic appearance in an asymptomatic patient.Semantic proximity Read ↗

Screening for Maternally Inherited Diabetes and Deafness in Large Cohorts of Hearing Impaired and Diabetic PatientsSemantic proximity Read ↗

Compound mitochondrial DNA mutations in a neurological patient with ataxia, myoclonus and deafness.Semantic proximity Read ↗

Clinical characteristics and hearing impairment in carriers of the m.3243 A > G variant.Semantic proximity Read ↗

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