Results 11 to 20 of about 1,975,307 (342)

Sickle Cell-Hemoglobin C Disease [PDF]

Dapim refuiim. Folia medica, 2020
A hemoglobinopathy that is considered a hybrid of sickle cell disease and hemoglobin C disease. Patients present with the symptoms of sickle cell disease but the latter are less frequent and severe compared to sickle cell disease.
National Cancer Institute
semanticscholar   +3 more sources

Impaired blood rheology plays a role in the chronic disorders associated with sickle cell-hemoglobin C disease

Haematologica, 2014
Lionnet et al. recently reported a high prevalence of retinopathy (RET) and otologic disorders (OTD) in patients with sickle cell-hemoglobin C disease (SC), while a significant number of patients had renal diseases (mainly glomerulopathy; GLO) and ...
Nathalie Lemonne, Yann Lamarre, Marc Romana, Marie-Dominique Hardy-Dessources, François Lionnet, Xavier Waltz, Vanessa Tarer, Danielle Mougenel, Benoît Tressières, Marie-Laure Lalanne-Mistrih, Maryse Etienne-Julan, Philippe Connes   +11 more
doaj   +4 more sources

Thalassemia—Hemoglobin C Disease [PDF]

Blood, 1954
Abstract An unusual type of severe chronic hypochromic microcytic anemia in a Negro is described and attributed to the interaction of the hemoglobin C gene with the thalassemia gene. The patient and his father were shown to be carriers of the C trait, the mother and several siblings of the thalassemia gene.
WOLF W. ZUELZER, EUGENE KAPLAN
openaire   +2 more sources

Regulation of cation content and cell volume in hemoglobin erythrocytes from patients with homozygous hemoglobin C disease. [PDF]

Journal of Clinical Investigation, 1985
Carlo Brugnara, Alan S. Kopin, H. Franklin Bunn, D. C. Tosteson   +3 more
openalex   +2 more sources

Hemoglobin C Disease With Splenomegaly and With Factor II Mutation Gene Thrombophilia: A Case Report. [PDF]

Cureus
Vázquez-Folch SJ, Jiménez-Berríos GA, Izquierdo N, Vazquez VJ.   +3 more
europepmc   +3 more sources

Hematological Profile of Hemoglobin C Disease: A Retrospective Study. [PDF]

Cureus
Regragui I, Mamad H, El Mokhtari N, Woumki A, Dahmani F, Benkirane S, Masrar A.   +6 more
europepmc   +3 more sources

Relationships between systemic vascular resistance, blood rheology and nitric oxide in children with sickle cell anemia or sickle cell-hemoglobin C disease

Clinical Hemorheology and Microcirculation, 2014
Yann Lamarre, Marie‐Dominique Hardy‐Dessources, Marc Romana, Marie‐Laure Lalanne‐Mistrih, Xavier Waltz, Marie Petras, Lydia Doumdo, Anne Blanchet‐Deverly, Jean Martino, Benoît Tressières, Frédéric Maillard, Vanessa Tarer, Maryse Etienne‐Julan, Philippe Connes   +13 more
openalex   +3 more sources

Iron deficiency and hemoglobin C disease [PDF]

The Journal of Pediatrics, 1995
P. Ehrhardt
openalex   +3 more sources

Red cell life span in sickle cell-hemoglobin C disease with a note about sickle cell-hemoglobin O ARAB [PDF]

Blood, 1975
PR McCurdy, Lana Othman Mahmood, AS Sherman   +2 more
semanticscholar   +5 more sources

MOLECULAR MECHANISM OF HEMOLYTIC ANEMIA IN HOMOZYGOUS HEMOGLOBIN C DISEASE [PDF]

Journal of Experimental Medicine, 1969
Erythrocytes from a patient with homozygous hemoglobin C disease were subjected to gradual osmotic dehydration by incubation in hypertonic saline. Serial observations of these cells before and after 4 and 12 hr incubation were carried out by means of ...
Lawrence S. Lessin, Wallace N. Jensen, Eric Ponder   +2 more
openalex   +2 more sources