PubMed Clinical Queries
This tool uses predefined filters to help you quickly refine PubMed searches on clinical or disease-specific topics. To use this tool, enter your search terms in the search bar and select filters before searching.
Results for Clinical Studies: Therapy/Broad
5 of 17 results sorted by: Most RecentSee all results in PubMed (17)
Cerebral folate transporter deficiency syndrome in three siblings: Why genetic testing for developmental and epileptic encephalopathies should be performed early and include the FOLR1 gene.
Am J Med Genet A. 2021. PMID: 34008900
Effects of endocrine disrupting chemicals on myelin development and diseases.
Neurotoxicology. 2021. PMID: 33352275 Review.
Oligodendroglial Lineage Cells in Thyroid Hormone-Deprived Conditions.
Stem Cells Int. 2019. PMID: 31182964 Free PMC article. Review.
Mutations in ACTL6B, coding for a subunit of the neuron-specific chromatin remodeling complex nBAF, cause early onset severe developmental and epileptic encephalopathy with brain hypomyelination and cerebellar atrophy.
Hum Genet. 2019. PMID: 30656450 Clinical Trial.
Overcoming Monocarboxylate Transporter 8 (MCT8)-Deficiency to Promote Human Oligodendrocyte Differentiation and Myelination.
EBioMedicine. 2017. PMID: 29111262 Free PMC article.