A potential therapeutic agent for sickle cell anaemia
<p>Sickle cell anaemia is an inherited disease in which red blood cells become rigid and change from the normal disc shape characteristic of these cells into a sickle-like shape. These abnormally shaped cells stack together and can obstruct small blood vessels, leading to severe pain and tissu...
محفوظ في:
| المؤلف الرئيسي: | Nature Research (16552612) (author) |
|---|---|
| منشور في: |
2016
|
| الموضوعات: | |
| الوسوم: |
إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
|
مواد مشابهة
-
First report of serological, molecular detection, and characterization of human parvovirus B19 infections among sickle cell anaemia patients in Khartoum State, Sudan
حسب: Khalid, Salman
منشور في: (2025) -
The role of preoperative transfusion in sickle cell disease, a systematic review and meta-analysis
حسب: Yasamin Abdu (15899155)
منشور في: (2024) -
Genotypic and Phenotypic Composition of Sickle Cell Disease in the Arab Population - A Systematic Review
حسب: Fateen Ata (14153304)
منشور في: (2023) -
Dilemma in approach to stroke in sickle cell disease patient: A case report
حسب: Lina Okar (14777164)
منشور في: (2022) -
Manifestations of HbSE sickle cell disease: a systematic review
حسب: Ibrahim Khamees (14153301)
منشور في: (2022)