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2 小时
on MSN
England to screen up to 100,000 newborns for more than 200 rare genetic disorders
The initiative could speed up diagnoses for rare genetic conditions that affect thousands of children every year. View on ...
health.economictimes.indiatimes
6 小时
Spinal Muscular Atrophy (SMA): A Common Genetic Disorder
Author: Dr Shrikant Jamdade, Clinical Geneticist, Mumbai Spinal Muscular Atrophy (SMA) is a common genetic disorder affecting ...
University of Manchester
21 小时
Cutting corners results in rare genetic diseases being undiagnosed, say scientists
Inaccurate naming of genetic diseases is resulting in some rare genetic diseases needlessly being undiagnosed, University of ...
3 天
Overland Park teen bikes 150 miles to raise awareness, hope for his rare genetic disorder
An Overland Park teen completed a 150-mile bike journey Sunday to raise awareness and hope for his rare genetic disorder.
2 天
Local mom says two-year-old is bullied for her looks. Now, she’s asking parents to help ...
Now, at two years old, Mirlee Janice Ramirez and her beautiful smile show how far they've come since KENS 5's Sarah Forgany ...
8 天
on MSN
US FDA approves IntraBio's drug for rare genetic disease
The U.S. Food and Drug Administration approved IntraBio's drug for a rare and fatal genetic disorder, the health regulator ...
5 天
Joint research by Indian, U.S. universities leads to discovery of new genetic brain disorder
This discovery is not only a breakthrough in understanding brain disorders, but also highlights the rising influence of ...
12 天
US FDA approves Zevra's treatment for rare genetic disease
The U.S. Food and Drug Administration approved Zevra Therapeutics' drug for a rare and fatal genetic disorder, making it the ...
11 天
Devastated family mourns loss of two-year-old Isabelle to rare genetic disorder
A mother is “absolutely broken” following the death of her two-year-old daughter, Isabelle Cooper, from a rare genetic ...
3 天
KP Govt to Give Free Treatment for Rare Genetic Disorder
The Khyber Pakhtunkhwa (KP) government is considering offering free treatment for patients with Spinal Muscular Atrophy (SMA) ...
The Daily Telegraph
12 天
Mother ‘absolutely broken’ after second child dies from rare genetic disorder
Isabelle Cooper died in the early hours of Thursday morning after being diagnosed with the same rare genetic disorder as Alexander, her three-year-old brother. Her mother, Dr Emily Cooper ...
9 天
on MSN
Biohaven’s stock surges as treatment slows progress of neurological disorder
Shares of Biohaven climbed 13% premarket on Monday after the biotech company said its treatment for a rare neurological ...
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