Ranger College Course Syllabus TECA 1318 Wellness of the Young Child (I1) Credit Hours: 3
Fall 2024 (241S) Instructor Informatio Page 1 Ranger College Course Syllabus TECA 1318 …

Objectives: Tanzania has the third highest birth rate of sickle cell anaemia (SCA) in Africa,
but few studies describe severity of complications or available treatments, especially in …

Sickle cell disease (SCD) is an inherited hemoglobinopathy caused by a variant (rs344) in
the HBB gene encoding the β-globin subunit of hemoglobin. Chronic hemolytic anemia and …

Biochemical and genetic markers of erectile dysfunction Page 154 ADVANCES IN CLINICAL
CHEMISTRY, VOL. 57 BIOCHEMICAL AND GENETIC MARKERS OF ERECTILE DYSFUNCTION …

Objective Attention, processing speed, executive functioning, and math difficulties are
common in youth with sickle cell disease (SCD) with silent cerebral infarcts (SCI). This study …

Background: Hemoglobinopathies are associated with significant morbidity and mortality.
Accurate epidemiologic data reflecting the number of hemoglobinopathy patients are lacking …

Research questions: clinical, epidemiological and Hematological characteristics of a cohort
of children with sickle cell anemia attending a specialist out-patient clinic in a rural hospital …

Una de las complicaciones neurológicas más devastadoras de la anemia drepanocítica son
los ictus, tanto isquémicos como hemorrágicos. El 11% de los pacientes con hemoglobina …

Objective: In sickle cell anemia, fever is a common presenting symptom and is frequently the
first indication of serious and life-threatening bacterial infection. There is a lack of study in …

We report a case of priapism in a 6-month-old boy of African descent who had been
receiving intravenous sildenafil, a phosphodiesterase-5 inhibitor. An orthotopic cardiac …