Hemoglobin H

01/01/2023 - "This study aimed to analyze the anemia characteristics in early pregnancy of pregnant women with hemoglobin H (Hb H) disease and their pregnancy outcomes, and to provide reference to the pregnancy management and treatment of these women. "
08/01/2023 - "Violin plots showed that carriers with co-inheritance of β-thalassaemia and mild α-thalassaemia expressed the lightest anemia, and carriers with co-inheritance of β-thalassaemia and hemoglobin H (Hb H) disease expressed the most severe anemia. "
01/01/2022 - "Hemoglobin H-Pakse (Hb H-PS) disease is a variant of non-deletional Hb H disease associated with various degrees of anemia. "
11/01/2018 - "Hemoglobin H (Hb H) disease is usually characterized by the existence of Hb H, which influences the degree of functional anemia. "
09/09/1957 - "[Case of hemoglobin H constitutional microcytic anemia]."

01/01/2021 - "Detection of rare hemoglobin H (HbH) inclusions in red cells in the peripheral blood is a common screening method for alpha-thalassemia. "
10/01/2015 - "Hemoglobin H identification by high-performance liquid chromatography in confirmed hemoglobin H disease."
11/01/2009 - "Hemoglobin H-constant spring in North America: an alpha thalassemia with frequent complications."
12/01/2005 - "In alpha-thalassemia disorders, structural mutations such as hemoglobin H-Constant Spring resulted in a severe hemoglobin H phenotype. "
09/01/2004 - "Hemoglobin H (HbH) disease is the most severe type among survivors of alpha-thalassemia. "

10/14/2021 - "The thalassemia of Hemoglobin H-Constant Spring disease (HbH-CS) is the most common type of Thalassemia in non-transfusion thalassemia. "
01/01/2021 - "Hemoglobin H (Hb H) disease is the most significant health problem of the α-thalassemia syndromes. "
01/01/2021 - "Hemoglobin H (HbH) disease is a moderately severe form of α-thalassemia. "
11/01/2020 - "Hemoglobin H (Hb H) disease can be caused by compound heterozygosity for two different mutations or from homozygotes for mutations, and conventional genetic methods may lead to misdiagnosis when Hb H disease is combined with a rare β-thalassemia. "
01/01/2018 - "Overall, 84 patients with α-thalassemia (62 deletional hemoglobin H; 22 nondeletional hemoglobin H), 39 with β-thalassemia (26 with homozygous or double heterozygous β mutations; 13 with single β mutations with or without α triplication), and 15 with E/β-thalassemia (12 E/β0 ; three E/β+ ) were identified. "

10/01/2019 - "In the current study Hemoglobin H (HbH) disease patients were analyzed as the most common form of thalassemia intermedia in Iran. "
01/01/2009 - "Hemoglobin H (Hb H) disease is the most common form of thalassemia intermedia and has many features that require careful consideration in management. "
01/01/1989 - "The growth in weight kept up with their presplenectomy period in 40/49 cases (81.63%) in beta-thalassemia/Hb E but there was no change in the weight velocity in hemoglobin H and beta-thalassemia major. "
01/01/1989 - "4. Within 2 years postoperatively, the growth velocity in height kept up with their presplenectomy period in hemoglobin H and beta-thalassemia major (except two cases). "
01/01/1973 - "Hemoglobin H-beta-thalassemia."

11/01/1996 - "We then used this system to study the in vitro susceptibility of RBCs from individuals with hemoglobin H (Hb H) disease to infection and growth of P. "
07/01/1999 - "Hereditary hemoglobin H (HbH) disease was diagnosed in 2 Japanese sisters who presented with aplastic crisis following acute human parvovirus B19 (HPV B19) infection. "
06/15/2003 - "Hemoglobin electrophoresis and brilliant cresyl blue staining revealed hemoglobin H (HbH) disease with an infection-associated hemolytic crisis. "