PubMed Clinical Queries
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Results for Clinical Studies: Therapy/Broad
5 of 5 results sorted by: Most RecentSee all results in PubMed (5)
Identification of MMACHC and ZEB2 mutations causing coexistent cobalamin C disease and Mowat-Wilson syndrome in a 2-year-old girl.
Clin Chim Acta. 2022. PMID: 35709987 Free article.
Syndromic Craniosynostosis Can Define New Candidate Genes for Suture Development or Result from the Non-specifc Effects of Pleiotropic Genes: Rasopathies and Chromatinopathies as Examples.
Front Neurosci. 2017. PMID: 29093661 Free PMC article. Review.
Psychopharmacological Management of Problem Behaviors in Mowat-Wilson Syndrome.
J Child Adolesc Psychopharmacol. 2015. PMID: 26402313 Free PMC article. No abstract available.
Mowat-Wilson syndrome: deafness in the first Egyptian case who was conceived by intracytoplasmic sperm injection.
J Child Neurol. 2014. PMID: 24282181
Epilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotype.
Am J Med Genet A. 2013. PMID: 23322667