Delayed Hemolytic Transfusion Reaction in Sickle Cell Disease

There is an extensive literature on numerical schemes for the drift-diffusion equa- tions: finite difference methods, finite elements methods, mixed exponential fitting finite

As already underlined, any regular geodesic ball veri- fies the condition of Theorem 1.4.1; so we recover the well-known results of existence and uniqueness of a martingale

Arterial stiffness, known as an indicator for macrovascular function, has been analysed in sickle cell adults [11,12] but whether arterial hardening also occurs in children

Dans cette revue, nous détaillons l’implication du système du complément dans l’hémolyse ainsi que ses conséquences dans la drépanocytose et l’hémolyse

To determine the chromosomal background

In the current study we tested 102 SCA Tunisian children patients among whom 52 have cholelithiasis and 76 subjects were chosen as control group characterized with normal

Several pathophysiological pathways in sickle cell disease (SCD), the most prevalent hemoglobinopathy worldwide, result in activation of circulating blood cells and

Gray dots, hemoglobin level for patients with the postartesunate delayed-onset hemolysis (PADH) pattern of anemia; black dots, hemoglobin level for patients with non-PADH pattern