PubMed Clinical Queries
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Results for Clinical Studies: Therapy/Broad
5 of 123 results sorted by: Most Recent
See all results in PubMed (123)-
A novel splice-altering TNC variant (c.5247A > T, p.Gly1749Gly) in an Chinese family with autosomal dominant non-syndromic hearing loss.
BMC Med Genomics. 2024. PMID: 39020321 Free PMC article.
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Low-intensity noise exposure takes an essential part in the mechanism of late-onset hereditary hearing loss caused by Abcc1 mutation.
Clin Genet. 2024. PMID: 38951883
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MEK Inhibition Enhances the Antitumor Effect of Radiotherapy in NF1-Deficient Glioblastoma.
Mol Cancer Ther. 2024. PMID: 38714355
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Effective TRIAC treatment of a THRβ-mutated patient with thyroid hormone resistance.
Endocrine. 2024. PMID: 38558372
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Mechanisms of pathogenicity and the quest for genetic modifiers of kidney disease in branchiootorenal syndrome.
Clin Kidney J. 2023. PMID: 38213489 Free PMC article.