Glanzmann thrombasthenia: deficient binding of von Willebrand factor to thrombin-stimulated platelets.
Glanzmann thrombasthenia is an inherited bleeding disorder characterized by the failure of platelets to aggregate in response to almost all stimuli. However, thrombasthenic platelets will aggregate with bovine and porcine von Willebrand factor (vWF) and will show normal ristocetin-induced binding an...
שמור ב:
| הוצא לאור ב: | Proc Natl Acad Sci U S A |
|---|---|
| Principais autores: | , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
National Academy of Sciences
1982
|
| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC347047/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6310559/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.79.19.6038 |
| תגים: |
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|
