hemoglobin New York

07/01/2022 - "Our study shows that the hematological characteristics of Hb New York combined with thalassemia are similar to the corresponding thalassemia, and Hb New York does not aggravate the clinical manifestations of thalassemia."
07/01/2022 - "However, the differences in MCV and MCH values were not statistically significant between Hb New York combined with β thalassemia and β thalassemia (P > 0.05). "
07/01/2022 - "When Hb New York heterozygotes were compared to Hb New York combined with β0 thalassemia or β+ thalassemia, the differences in MCV and MCH values were statistically significant (P < 0.05). "
07/01/2022 - "The HGB, MCV and MCH values of α thalassemia patients were not different from Hb New York combined with α thalassemia group (P > 0.05). "
07/01/2022 - "Hb New York, preliminary results concerning the hematologic characteristics and the effects on thalassemia."

01/01/2016 - "CE may be the preferred method for hemoglobinopathy screening in areas with high prevalence of Hb New York."
01/01/2019 - "Additionally, Hb Q-Thailand hemoglobinopathy and five other types of hemoglobinopathies (Hb New York, Hb J-Bangkok, Hb G-Taipei, Hb G-Coushatta and Hb Maputo) were found. "
11/12/2021 - "We found that Hb Q-Thailand is the most common, and other types of hemoglobinopathies are followed by Hb E, Hb New York, Hb G-Chinese, Hb G-Coushatta, Hb J-Bangkok, Hb J-Broussais, Hb Ottawa, and Hb G-Taipei. "

12/01/2008 - "Hemoglobin New York is not a matter in prenatal screening and diagnosis for beta-thalassemia."
04/01/2008 - "An extended family with three individuals affected by two different forms of double heterozygosity for beta-thalassemia and Hb New York is reported. "

01/01/1980 - "Hemoglobin New York associated with alpha-thalassemia."
04/01/2008 - "Double heterozygosity for Hb New York [beta 113 GTG-->GAG; VAL-->GLU] and beta degrees-thalassemia mutations manifests as a thalassemia trait."
01/01/1980 - "A Chinese family is described in which 6 members possess both the beta-chain hemoglobin variant Hb New York and alpha-thalassemia trait. "

08/01/2013 - "HGB, MCV and MCH of Hb New York heterozygous and Hb New York composited WS heterozygous were normal, and patients with Hb New York composited SEA heterozygous showed mild anemia, decreased MCV and MCH. "
01/01/1988 - "One patient who inherited classical Hb H disease and Hb New York (NY) [alpha 113(G15)Val----Glu] had severe anemia, and required frequent blood transfusions due to the deleterious effect of an increased alpha-NY chain turnover.(ABSTRACT TRUNCATED AT 250 WORDS)"
08/01/2013 - "Hb New York heterozygous had normal hematological phenotype, ant combined with other types of thalassemia could exhibit symptoms such as anemia."