A novel GLRB mutation in neonatal hyperekplexia with divergent EEG findings: a case series. [PDF]
Tamimi M +7 more
europepmc +1 more source
Rafiq Syndrome: Old Variant in MAN1B1 Gene and Some New Phenotypic Features. [PDF]
Özgün N, Saka Güvenç M.
europepmc +1 more source
Rare missense variants in <i>FNDC1</i> are associated with severe adolescent idiopathic scoliosis. [PDF]
Charng WL +16 more
europepmc +1 more source
Network pharmacology and molecular dynamics simulations reveal shared mechanisms and myopia-specific targets of atropine in myopia and dry eye disease. [PDF]
Lin M, Shu W, Hua G, Duan Z, Qu J, Hu L.
europepmc +1 more source
Bioinformatic analysis of endometrial miRNA expression profile at day 26-28 of pregnancy in the mare. [PDF]
Sadowska A +8 more
europepmc +1 more source
Hyperekplexia: Unveiling a Rare Neurological Condition With a Treatable Solution. [PDF]
Aglave NR +3 more
europepmc +1 more source
New Dihalogenated Derivatives of Condensed Benzimidazole Diones Promotes Cancer Cell Death Through Regulating STAT3/HK2 Axis/Pathway. [PDF]
Aleksandrova Y +9 more
europepmc +1 more source
Molecular entities for the anti-melanoma effect of <i>Solanum nigrum</i>. [PDF]
Sakharkar N +3 more
europepmc +1 more source
New insights into neurodevelopmental disorders by whole genome sequencing of 100 families from Italy. [PDF]
Spirito G +30 more
europepmc +1 more source
Fluoxetine minimally affects hearing loss but induces gene expression changes in the cochlear nuclei after noise exposure. [PDF]
An HJ, Choi S, Lee S, Yeo H, Kim SY.
europepmc +1 more source

