MH Steinberg, RP Hebbel - Am J Hematol, 1983 - interscience.wiley.com There is a great diversity in the clinical manifestations of sickle cell anemia. Some patients have
severe repetitive infarctive episodes culminating in organ failure. Others have minor and nonincapacitating
problems. This review focuses on the cellular and genetic factors that may play a role in ... Cited by 42 - Related articles - All 2 versions
RL Nagel, MH Steinberg - Pediatric Pathology and Molecular Medicine, 2001 - gfdl.gov Π Sickle hemoglobin is the product of one mutated gene, but the disease phenotype is the product
of many genes. Polymorphism among the genes responsible for the pleotropic eÚects can be
epistatic (or modi®er) genes contributing to interindividual variation that characterizes ... Cited by 22 - Related articles - View as HTML - BL Direct - All 5 versions
- ►haematologica.com [PDF] A Pietrapertosa, A Palma, D Campanale, G Delios, … - …, 2001 - haematologica.com Background and Objectives. Glucose-6-phosphate dehy- drogenase (G6PD) deficiency is the
most common ery- throcytic enzymatic disorder in Italy and is characterized by wide clinical, biochemical
and molecular variability. We studied the clinical and hematologic data from 54 G6PD- ... Cited by 17 - Related articles - BL Direct - All 15 versions
SC Bernstein, JE Bowman, LK Noche - Human Heredity, 1980 - content.karger.com The prevalence of glucose-6-phosphate dehydrogenase (G6PD) deficiency and sickle cell trait
was determined in 371 Cameroonian males and 668 male blood donors in Chicago. The number
of males with both sickle cell trait and G6PD deficiency was significantly greater than ... Cited by 16 - Related articles - All 4 versions
WN Gibbs, J Wardle, GR Serjeant - Br. J. Haematol, 1980 - interscience.wiley.com Summary. The relationship between D-glucose-6-phosphate: NADP oxido-reduc-tase
(ECI1.1.49; glucose-6-phosphate dehydrogenase; G6PD) deficiency and homozygous sickle
cell (SS) disease was examined in 120 patients. The proportion of hemizygotes (22-6%) ... Cited by 16 - Related articles - All 3 versions
S Diop, D Thiam, A Sene, M Cisse, К Fall, … - Médecine d'Afrique …, 2000 - santetropicale.com La drépanocytose et le déficit en G-6-PD sont deux ano- malies génétiques retrouvées avec
des prévalences simi- lai res de 8 à 10 % au Sénégal. Notre objectif était de d é te rminer la prévalence
du déficit en G-6-PD et de rechercher une influence éventuelle sur le profil évolutif de la ... Cited by 2 - Related articles - View as HTML - All 2 versions
RL Plasmar - 2004 - books.google.com Focus ON SICKLE CELL RESEARCH Thi s One 4X87-3XN-USNC ... Focus ON SICKLE CELL
RESEARCH RALPH L. PLASMAR EDITOR Nova Biomedical Books New York ... Production
Coordinator: Donna Dennis Coordinating Editor: Tatiana Shohov Senior Production ... Related articles - All 2 versions
G DOUGLAS - ltdk.helsinki.fi THOUGH THE ORIGINS of erythrocyte glucose-6-phosphate dehydrogenase (G-6-PD) deficiency
are rooted in human antiquity, the presence of drug-induced hemolysis in indi- viduals subsequently
felt to have G-6-PD deficiency was first reported in 1926 and the biochemical lesion ... Related articles - View as HTML
[CITATION] Last literature review version 17.1: Thu Jan 01 00: 00: 00 GMT 2009| This topic last …
