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

Prevalence and progression of mitochondrial diseases: a study of 50 patients.

Muscle & nerve - 1 Dec 2003

Arpa Javier, Cruz-Martínez Antonio, Campos Yolanda, Gutiérrez-Molina Manuel, García-Rio Francisco, Pérez-Conde Concepción, Martín Miguel A, Rubio Juan C, Del Hoyo Pilar, Arpa-Fernández Ana, Arenas Joaquín

Abstract excerpt

We report 50 patients with various clinical phenotypes of mitochondrial disease studied over the past 10 years in a large urban area (Madrid Health Area 5). The clinical phenotypes showed a large variety of abnormalities in molecular biology and biochemistry. The prevalence of mitochondrial diseases was found to be 5.7 per 100,000 in the population over 14 years of age. Clinical and electrophysiological...

Read the complete abstract on PubMed

Topics

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

Share to Electromyography
Share to Epilepsies, Myoclonic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lactic Acid

Share to MELAS Syndrome

Share to Mitochondrial Diseases

Share to Neural Conduction

Share to Ophthalmoplegia, Chronic Progressive External

Source

Identifiers

PMID: 14639582
DOI: 10.1002/mus.10507

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prevalence and progression of mitochondrial diseases: a study of 50 patients.PMID 14639582Read ↗

Mitochondrial diseases: clinical considerations.Semantic proximity Read ↗

Natural history of mitochondrial disorders: a systematic review.Semantic proximity Read ↗

The Genetic Landscape of Mitochondrial Diseases in Spain: A Nationwide Call.Semantic proximity Read ↗

The epidemiology of mitochondrial disorders--past, present and future.Semantic proximity Read ↗

[Clinical and investigative approaches in mitochondrial diseases. A review of 15 cases].Semantic proximity Read ↗

Clinical phenotype of mitochondrial diabetes due to rare mitochondrial DNA mutations.Semantic proximity Read ↗

[Mitochondrial respiratory chain diseases. Evaluation and variability in 52 patients].Semantic proximity Read ↗

Incidence and predictors of total mortality in 267 adults presenting with mitochondrial diseases.Semantic proximity Read ↗

Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluation.Semantic proximity Read ↗

Adult-onset mitochondrial movement disorders: a national picture from the Italian Network.Semantic proximity Read ↗

Myotonic dystrophy type 1: 13 years of experience at a tertiary hospital. Clinical and epidemiological study and genotype-phenotype correlation.Semantic proximity Read ↗

Mitochondrial myopathy, cardiomyopathy and psychiatric illness in a Spanish family harbouring the mtDNA 3303C > T mutation.Semantic proximity Read ↗

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