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Live Science on MSNMoebius syndrome: The rare condition that makes people unable to smileMoebius syndrome is a rare condition that affects several cranial nerves, impairing the muscles that control facial ...
Ocugen ( NASDAQ: OCGN) disclosed on Tuesday that its gene therapy candidate, OCU410ST, has been granted rare pediatric ...
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News-Medical.Net on MSNAre children’s eyes at risk? Study links tech habits to eye structure differencesDigital device use and reading distance are linked to changes in choroidal thickness among Tokyo children. The study finds ...
Background: This study was performed to assess the prevalence of dry eye syndrome and diabetic retinopathy (DR) in type 2 diabetic patients and their contributing factors. Methods: 199 type 2 ...
At ARVO 2025, in Salt Lake City, Utah, Anisha Kasi talked about her presentation on how her team used the TriNetX database, a large database of over 150 million patients worldwide, to validate the ...
Noonan syndrome with multiple lentigines (NSML) is a RASopathy characterized by features of multiple lentigines, ECG conduction abnormalities, ocular hypertelorism, pulmonary stenosis, abnormalities ...
The cDNAs encoding RAF1 mutants were generated by PCR and inserted into pCDNA3.1(+) vector with N-terminal FLAG tag. Plasmids were transfected into 293T cells by using lipofectamine 2000 (Invitrogen), ...
A focused evaluation of scalp hair should be part of every newborn physical assessment. Although typically completed in the delivery room, it may be useful to re-evaluate the infant after the ...
South West Thames Regional Genetic Service, St George's Hospital Medical School, London. Eleven families with Noonan syndrome in either two or three generations have been identified. Following the ...
MENTRI Besar Selangor Inc (MBI Selangor), which administers assets and investments of the state government, is exploring a presence in banking. Sources say the state investment arm is eyeing to ...
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