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

Gentamicin treatment in McArdle disease: failure to correct myophosphorylase deficiency.

Neurology - 24 Jan 2006

Schroers A, Kley R A, Stachon A, Horvath R, Lochmüller H, Zange J, Vorgerd M

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 Energy Metabolism
Share to Gentamicins
Share to Glycogen Storage Disease Type V
Share to Magnetic Resonance Spectroscopy

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

Share to Muscle, Skeletal

Share to Myoblasts

Share to Osmolar Concentration

Share to Phosphorylases

Source

Identifiers

PMID: 16434679
DOI: 10.1212/01.wnl.0000194212.31318.fc

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 10 closest

Gentamicin treatment in McArdle disease: failure to correct myophosphorylase deficiency.PMID 16434679Read ↗

Cell models for McArdle disease and aminoglycoside-induced read-through of a premature termination codon.Semantic proximity Read ↗

Myophosphorylase deficiency: an unusually severe form with myoglobinuria.Semantic proximity Read ↗

Molecular characterization of myophosphorylase deficiency (McArdle disease) in 34 patients from Southern France: identification of 10 new mutations. Absence of genotype-phenotype correlation.Semantic proximity Read ↗

Two novel missense mutations (E654K, L396P) in Caucasian patients with myophosphorylase deficiency (McArdle's disease).Semantic proximity Read ↗

A novel mutation in the PYGM gene in a family with pseudo-dominant transmission of McArdle disease.Semantic proximity Read ↗

Three new mutations in patients with myophosphorylase deficiency (McArdle disease).Semantic proximity Read ↗

Successful perioperative management of a patient with primary systemic carnitine deficiency: a case report.Semantic proximity Read ↗

McArdle's disease-muscle glycogen phosphorylase deficiency.Semantic proximity Read ↗

Gentamicin treatment of Duchenne and Becker muscular dystrophy due to nonsense mutations.Semantic proximity Read ↗

Aminoglycoside antibiotics restore dystrophin function to skeletal muscles of mdx mice.Semantic proximity Read ↗

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