haemophilia

World Hemophilia Day|Care for "glass people" and make life no longer fragile
haemophilia
04-17
A diseased chromosome that nearly ruined most of the European royal family...
chromosome haemophilia Queen Victoria
04-18
On World Hemophilia Day| how do they get out of their pain and live their lives?
World Hemophilia Day haemophilia Hemophilia patients Huang Jiancong
04-17
"I don't want to bleed anymore..." In the face of such patients, doctors hope that they can be "bear children"
doctor Bear children_parenting Hemophilia a haemophilia
04-17
The doctor saved a life with one sentence, and the family tearfully said, "Shou yi is no longer needed!" ”
doctor haemophilia icu Hemophilia patients Jin Jie
04-17
Most afraid of children growing up? This genetic disease makes them spend tens of thousands of yuan more for every pound of meat they grow
Genetic disorders haemophilia Hemophilia patients
04-17
22 years to achieve hemophilia patients "zero payment" for drugs
Hemophilia patients haemophilia Sun Jing
04-17
This 16-year-old boy is very "squeamish" and can't be bumped or touched! After knowing the truth, I actually cried!
haemophilia child Hemophilia patients
04-08
"I am not a medicine god" is another example, should Roche Pharmaceutical reduce the price of life-saving drugs?
Roche Pharmaceuticals Emmy Beads Coagulation factor haemophilia Hemophilia patients
04-06
Brave the forbidden area of life| the Concord Liver Surgery team removed liver tumors for patients with hemophilia
Peking Union Medical College Hospital liver surgery Hemophilia patients haemophilia
03-23
Hemophilia, "passing on men to women"?
haemophilia Coagulation factor X chromosome Hemophilia patients
03-14
Yang Linhua, deputy to the National People's Congress: Suggested solving the "last mile" of drugs for patients with rare diseases
Poplar flowers haemophilia Coagulation factor Hemophilia patients Deputy to the National People's Congress hospital Coronavirus
03-03
With about 350 million people sick worldwide, how far are we from overcoming the rare disease problem?
Spinal muscular atrophy Auggie haemophilia Muscle atrophy
02-28
The annual drug cost of hemophilia is 1.2 million, and patients have difficulty in taking medicines! Roche Pharma: China pricing has been low
haemophilia Roche Pharmaceuticals Shu YouLile Emmy Beads
02-25
Rare Diseases Catalogue Impact Assessment: 140,000 people are waiting for a second life
haemophilia Bright drugs Hemophilia patients Guan Tao
02-18
Remind parents: these 5 diseases are easy to inherit to the next generation, and you need to do a good job of prevention in advance!
heredity parents diabetes hypertension Allergic constitution haemophilia
02-10
How much is a three-generation test tube at a time, and what is the process?
test tube embryo infant Third generation test tubes haemophilia Genetic diseases ovum
01-05