Results 81 to 90 of about 11,475 (240)
Abstract Background Blood transfusion remains a cornerstone in the management of sickle cell disease (SCD); however, it is frequently complicated by red cell alloimmunisation. A significant debate persists within the scientific community regarding the optimal strategy to mitigate this risk: the traditional, pragmatic approach of serologic phenotyping ...
Christiane Ruffato Carminati +6 more
wiley +1 more source
Genetic Disease Burden, Nutrition and Determinants of Tribal Health Care in Chhattisgarh State of Central-East India: A Status Paper [PDF]
Tribal health is an important aspect of development and progress of the people. This study pertaining to genetic disease burden, nutritional status and biomedical anthropological assessment with particular reference to determinants of tribal health care ...
Balgir, RS
core +1 more source
Genetic diversity in RHD and RHCE genes among a selected Kenyan blood donor population
Abstract Background Serologic typing for ABO and RhD is standard in transfusion services, with extended serology and genotyping performed to reduce red cell alloimmunization risk. In Kenya, RH typing is limited to RhD, and genotyping is unavailable. This study used RHD/RHCE genotyping to predict phenotypes and their distribution in a Kenyan blood donor
Sandra A. Sowah +8 more
wiley +1 more source
Acquired hemoglobin C secondary to transfusion with antigen‐matched red blood cells [PDF]
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/107569/1/jca21306 ...
Arps, David P. +2 more
core +1 more source
Codocytosis in the Dog: 345 Cases (2020–2022)
ABSTRACT Introduction Codocytes, or target cells, are a morphologic variation of erythrocytes characterized by increased membrane surface area relative to volume. In dogs, codocytosis is frequently noted on blood smear evaluation, but its clinical significance remains poorly understood. Objectives To characterize the clinical conditions associated with
Sarena M. Krojanker +5 more
wiley +1 more source
Asymtomatic essential thrombocythemia in a child: a rare case report
Essential thrombocythemia is a rare myeloproliferative disorder in pediatrics. This myeloproliferative disorder is charactherized by thrombocytosis and hyperplasia of megakaryocytes in the bone marrow. Other cell lines are not involved.JAK2V617Fmutations
Majid Vafaie +4 more
doaj
Background: Nearly 226 million carriers of thalassemias and abnormal hemoglobin are present worldwide according to the World Health Organization (WHO). The laboratory plays an important role in the investigation of the thalassemias and hemoglobinopathies.
R Jha
doaj +1 more source
Inter-Rater Reliability of the CASCADE Criteria: Challenges in Classifying Arteriopathies. [PDF]
Background and purposeThere are limited data about the reliability of subtype classification in childhood arterial ischemic stroke, an issue that prompted the IPSS (International Pediatric Stroke Study) to develop the CASCADE criteria (Childhood AIS ...
Amlie-Lefond, Catherine +18 more
core +1 more source
Abstract Blood transfusion is life‐saving for patients in emergencies, but low‐ and middle‐income countries (LMICs) often face a severe shortage of banked blood. Establishing blood banks in rural areas presents substantial logistical and economic challenges for many LMICs.
Suvro Sankha Datta +4 more
wiley +1 more source
BACKGROUND: Thalassemia is a hereditary hemoglobinopathy characterized by inadequate or absent globin synthesis. This study aims to assess the prevalence and incidence of chronic pain in individuals with thalassemia within our population and further ...
Adel F. Al-Marzouki +12 more
doaj +1 more source

