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

Asymmetrical leg atrophy in levodopa-responsive dystonia due to a novel GTP cyclohydrolase mutation.

Movement disorders : official journal of the Movement Disorder Society - 1 Mar 2014

Mulroy Eoin, McCarthy Allan, Lynch Tim, Costello Danny, Ross Owen A

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 Atrophy
Share to Dystonia
Share to Genetic Predisposition to Disease
Share to Genetic Testing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to GTP Cyclohydrolase

Share to Levodopa

Share to Mutation

Source

Open in PubMed Open full text

Identifiers

PMID: 24474670
DOI: 10.1002/mds.25813
PMCID: PMC4389628

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

Asymmetrical leg atrophy in levodopa-responsive dystonia due to a novel GTP cyclohydrolase mutation.PMID 24474670Read ↗

Gene symbol: GTP cyclohydrolase I (GCH-I). Disease: dopa-responsive dystonia.Semantic proximity Read ↗

A novel missense mutation of the GTP cyclohydrolase 1 gene in a Taiwanese family with dopa-responsive dystonia: A case report.Semantic proximity Read ↗

Two in the hand, an essential lesson in tremor management.Semantic proximity Read ↗

Complex hyperkinetic movement disorders associated with POLG mutations.Semantic proximity Read ↗

Dopa-responsive dystonia presenting as delayed and awkward gait.Semantic proximity Read ↗

A novel de novo point mutation in the GTP cyclohydrolase I gene in a Japanese patient with hereditary progressive and dopa responsive dystonia.Semantic proximity Read ↗

Growth hormone deficiency in a dopa-responsive dystonia patient with a novel mutation of guanosine triphosphate cyclohydrolase 1 gene.Semantic proximity Read ↗

Tetrahydrobiopterin metabolism and GTP cyclohydrolase I mutations in L-dopa-responsive dystonia.Semantic proximity Read ↗

Benign lower limb amyotrophy due to TARDBP mutation or post-polio syndrome?Semantic proximity Read ↗

A case of parkinsonism and dopa-induced severe dyskinesia associated with novel mutation in the GTP cyclohydrolase I gene.Semantic proximity Read ↗

Case Report: Guitarist’s cramp as the initial manifestation of dopa-responsive dystonia with a novel heterozygous GCH1 mutationSemantic proximity Read ↗

Dopa-responsive dystonia with a novel initiation codon mutation in the GCH1 gene misdiagnosed as cerebral palsy.Semantic proximity Read ↗

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