نتایج جستجو برای: sickle cell anemia

تعداد نتایج: 1724247  

2013
Alexandra M. Hogan Paul T. Telfer Fenella J. Kirkham Michelle de Haan

Executive dysfunction occurs in sickle cell anemia, but there are few early data. Infants with sickle cell anemia (n = 14) and controls (n = 14) performed the "A-not-B" and Object Retrieval search tasks, measuring precursors of executive function at 9 and 12 months. Significant group differences were not found. However, for the A-not-B task, 7 of 11 sickle cell anemia infants scored in the lowe...

Journal: :Al-Azhar International Medical Journal (Print) 2023

Background: Sickle cell disease is an autosomal recessive characterized by aberrant production of hemoglobin S (HbS). The disease's presentation and severity varied substantially between people from various socioeconomic backgrounds geographical regions. clinical picture includes hemolytic anemia, vascular occlusion events, acute persistent pain, organ damage. Objective: To investigate the hema...

2012
Jacqueline N. Milton Paola Sebastiani Nadia Solovieff Stephen W. Hartley Pallav Bhatnagar Dan E. Arking Daniel A. Dworkis James F. Casella Emily Barron-Casella Christopher J. Bean W. Craig Hooper Michael R. DeBaun Melanie E. Garrett Karen Soldano Marilyn J. Telen Allison Ashley-Koch Mark T. Gladwin Clinton T. Baldwin Martin H. Steinberg Elizabeth S. Klings

Serum bilirubin levels have been associated with polymorphisms in the UGT1A1 promoter in normal populations and in patients with hemolytic anemias, including sickle cell anemia. When hemolysis occurs circulating heme increases, leading to elevated bilirubin levels and an increased incidence of cholelithiasis. We performed the first genome-wide association study (GWAS) of bilirubin levels and ch...

2011
Paulo Florentino Teixeira Neto Romélia Pinheiro Gonçalves Darcielle Bruna Dias Elias Cleiton Pinheiro de Araújo Hemerson Iury Ferreira Magalhães

BACKGROUND Sickle cell anemia is a hemoglobinopathy caused by a mutation that results in the production of an abnormal hemoglobin molecule, hemoglobin S (Hb S). This is responsible for profound physiological changes, such as the sickling of red blood cells. Several studies have shown that hydroxyurea protects against vaso-occlusive crises. OBJECTIVE The aim of this study was to evaluate the o...

2015
Jacqueline Faria de Oliveira Natália Gomes Vicente Juliana Pereira Pontes Santos Virgínia Resende Silva Weffort Jacqueline Faria de Oliveira Natália Gomes Vicente Juliana Pereira Pontes Santos Virgínia Resende Silva Weffort

OBJECTIVE To review the literature about the prevalence of vitamin D deficiency and its consequences in children and adolescents with sickle-cell disease. DATA SOURCES The literature survey was performed through the bibliographic databases Medline; U.S. National Library of Medicine and National Institutes of Health (PubMed); Literatura Latino-Americana e do Caribe em Ciências da Saúde (Lilacs...

Journal: :Pediatric dentistry 2014
Elizabeth Ralstrom Marcio A da Fonseca Melissa Rhodes Homa Amini

PURPOSE The purpose of this study was to characterize the impact of sickle cell disease (SCD) on oral health and examine its impact on quality of life. METHODS Fifty-four study subjects were recruited from the sickle cell clinic and 52 control subjects from the adolescent medicine clinic at Nationwide Children's Hospital, Columbus, Ohio. A dental exam was performed to determine each participa...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1981
R F Geever L B Wilson F S Nallaseth P F Milner M Bittner J T Wilson

Several reports have been published on the use of polymorphisms found in the human hemoglobin genes as a means for prenatal diagnosis of sickle cell anemia. The disadvantages of this approach reside in its limited application and the need for family analysis. Here we report that, by use of restriction endonuclease Dde I and diazobenzyloxymethyl-paper transfer procedures, a direct analysis can b...

Journal: :Jornal de pediatria 2014
Mona Kamal El-Ghamrawy Wagdi Maurice Hanna Amina Abdel-Salam Marwa M El-Sonbaty Eman R Youness Ahmed Adel

OBJECTIVE the present study was conducted to investigate the oxidant-antioxidant status in Egyptian children with sickle cell anemia. METHODS the serum levels of total antioxidant capacity (TAO), paraoxonase (PON), vitamin E, nitrite, and malondialdehyde (MDA) were measured in 40 steady state children with homozygous sickle cell anemia (24 males and 16 females) and 20 apparently healthy age- ...

2015
Juliane Almeida Moreira Marília Rocha Laurentino Rosângela Pinheiro Gonçalves Machado Maritza Cavalcante Barbosa Ronaldo Pinheiro Gonçalves Amanda de Menezes Mota Lilianne Brito da Silva Rocha Alice Maria Costa Martins Alcínia Braga de Lima Arruda Iêda Pereira de Souza Romélia Pinheiro Gonçalves

OBJECTIVE This study aimed to evaluate the influence of fetal hemoglobin (Hb F) on hemolysis biomarkers in sickle cell anemia patients. METHODS Fifty adult sickle cell anemia patients were included in the study. All patients were taking hydroxyurea for at least six months and were followed at the outpatient clinic of a hospital in Fortaleza, Ceará, Brazil. The control group consisted of 20 he...

Journal: :Blood 1983
T J Ley J DeSimone C T Noguchi P H Turner A N Schechter P Heller A W Nienhuis

We previously demonstrated that 5-azacytidine can selectively increase gamma-globin synthesis in a patient with beta +-thalassemia, prompting us to treat two patients with sickle cell anemia and two additional patients with beta + thalassemia. 5-Azacytidine (2 mg/kg/day) was continuously infused for 7 days with no apparent clinical toxicity. The gamma/beta-globin biosynthetic ratio increased fo...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید