A clinical research team from the LKS Faculty of Medicine, the University of Hong Kong (HKUMed), and international genetic researchers led a global research study using multi-omics analysis and ...
GRIN Therapeutics, Inc., a leader in the development of therapies to treat serious neurodevelopmental disorders, today announced that the U.S. Food and ...
4 天on MSN
A clinical research team from the LKS Faculty of Medicine, the University of Hong Kong (HKUMed), and international genetic researchers led a global research study using multi-omics analysis and ...
6 天
Medpage Today on MSNFirst-Ever Prenatal Treatment for Spinal Muscular Atrophy Shows PromiseThe first prenatal therapy for spinal muscular atrophy (SMA) showed promising results, a case report indicated. More than 2 ...
8 天
SussexWorld on MSN‘Selfless couple’ are Resident of the Month winnersA ‘selfless couple’ couple have been named joint recipients of the Horsham Resident of the Month award for January.
Researchers from the LKS Faculty of Medicine at the University of Hong Kong (HKUMed) and international genetic scientists have identified a new gene, DDX39B, linked to a rare neurodevelopmental ...
In a global study led by Dr Brian Chung Hong-yin (left), the HKUMed research team identifies a novel gene, DDX39B, for a rare disease. Genetic ...
HDFN has affected 2 of Andrea Renzi's 5 children and turned her into an activist on behalf of other mothers and families touched by the disease.
Katie Price's eldest son Harvey, who weighs 28 stone, suffers from the genetic disorder Prader-Willi syndrome, which causes ...
A MUM says her baby was “born with a broken heart” on Valentine’s Day and doctors told her to “kiss her and say goodbye” ...
Parinita Jain was performing at her cousin’s sangeet function where she collapsed on stage after thirty seconds of dancing ...
Lissencephaly refers to a genetic condition that leads to brain changes during fetal development. uncommon neurological condition that often results in severe developmental delays and difficult to ...
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