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Publications by Y. Gotoda

Mutations Producing Premature Termination of Translation and an Amino Acid Substitution in the Sterol 27-Hydroxylase Gene Cause Cerebrotendinous Xanthomatosis Associated With Parkinsonism

Journal of Neurology, Neurosurgery and Psychiatry
PsychiatryMental HealthNeurologySurgery
1999English

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Cerebrotendinous Xanthomatosis

2020English

Exonic Mutations in the SLC12A3 Gene Cause Exon Skipping and Premature Termination in Gitelman Syndrome

Journal of the American Society of Nephrology : JASN
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2014English

Electrophysiological Studies in Cerebrotendinous Xanthomatosis.

Journal of Neurology, Neurosurgery and Psychiatry
PsychiatryMental HealthNeurologySurgery
1992English

Cerebrotendinous Xanthomatosis

2005English

Cerebrotendinous Xanthomatosis

Archives of Neurology
2002English

Sterol 27-Hydroxylase Gene Dosage and the Anti-Atherosclerotic Effect of Rifampicin in Mice

Bioscience Reports
BiochemistryCell BiologyMolecular BiologyBiophysics
2018English

Pulmonary Manifestations in Cerebrotendinous Xanthomatosis.

Internal Medicine
Internal MedicineMedicine
1998English

Premature Termination Codon Mutations in the Von Willebrand Factor Gene Are Associated With Allele-Specific and Position-Dependent mRNA Decay

Haematologica
Hematology
2009English

Clinical Relevance of Brain Volume Changes in Patients With Cerebrotendinous Xanthomatosis

Journal of Neurology, Neurosurgery and Psychiatry
PsychiatryMental HealthNeurologySurgery
2010English

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