Zobrazeno 1 - 10
of 58
pro vyhledávání: '"hemoglobin D Punjab"'
Publikováno v:
Journal of Marine Medical Society, Vol 25, Iss 3, Pp 74-79 (2023)
Introduction: Hemoglobin D Punjab is a common hemoglobin D variant, which is essentially known to cause a mild disease even in homozygous state. Heterozygous state of hemoglobin D Punjab with sickle cell is the only presentation when a severe disease
Externí odkaz:
https://doaj.org/article/9581a1e22d1940f7b0890fc0d2befb7a
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
BackgroundSickle cell disease is an inherited disorder characterized by the presence of sickle hemoglobin (HbS). The process of Hb molecule polymerization is a pivotal step in the sickling process. Voxelotor, a recently approved novel therapeutic age
Externí odkaz:
https://doaj.org/article/9322b2f79ae640a8a92be39d7c6d3d92
Autor:
Tushar Kanti Biswas, Anupa Pillai
Publikováno v:
MGM Journal of Medical Sciences, Vol 6, Iss 3, Pp 148-151 (2019)
A 62-year-old woman with no comorbidity presented with dyspnea since 2 months and fatigue since 1 month. She was having severe anemia with hepatosplenomegaly and icterus. Anemia due to blood loss was ruled out. With a history of blood transfusions an
Externí odkaz:
https://doaj.org/article/f58cc0d5990948bb948466dc95d0d3e9
Publikováno v:
Asian Journal of Transfusion Science, Vol 11, Iss 2, Pp 199-202 (2017)
Hemoglobin (Hb) D-Punjab [β 121(GH4) Glu→ln; HBB: C.364G>C] and β0-thalassemia 3.4 kb deletion are very rare in the Thai population. For the first time, the coinheritance of HbD-Punjab with β0-thalassemia 3.4 kb deletion was reported in a 7-year
Externí odkaz:
https://doaj.org/article/3629c87b85f146f6a6aa9a5c653b01b7
Publikováno v:
مجله دانشگاه علوم پزشکی گرگان, Vol 17, Iss 1, Pp 108-113 (2015)
Background and Objective: Hemoglobin D-Punjab is one of the variant of hemoglobin caused by a mutation on position 121 of beta globin gene which is frequent in India, Pakistan and Iran. Heterozygote form of this variant is mainly asymptomatic while i
Externí odkaz:
https://doaj.org/article/32c71a4f4cd44126b1832805b8341b8e
Autor:
Abdul-Kader Souid, Srdjan Denic
Publikováno v:
European Journal of Medical and Health Sciences. 3:90-94
Hemoglobin D-Punjab is the most common variant of hemoglobin D. In premarital screening, molecular testing is often unavailable, and diagnosis (and marriage guidance) often relies on the hemoglobin analysis, family studies and epidemiological facts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96b721653e074c21d879cbe7bc687174
https://doi.org/10.24018/ejmed.2021.3.1.681
https://doi.org/10.24018/ejmed.2021.3.1.681
Publikováno v:
Journal of Dr. NTR University of Health Sciences, Vol 4, Iss 4, Pp 266-268 (2015)
Hemoglobinopathies constitute the most common genetic diseases in the world. In India, both beta-thalassemia and structural hemoglobin variants, such as hemoglobin S (HbS), hemoglobin D (HbD), and hemoglobin E (HbE), are common and pose significant h
Externí odkaz:
https://doaj.org/article/74a0f2c81ed942c09a63ebd3f7f85cba
Akademický článek
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Publikováno v:
مجله دانشگاه علوم پزشکی گرگان, Vol 15, Iss 2, Pp 65-69 (2013)
Background and Objective: Hemoglobinopathies are among the most prevalent genetic disorders worldwide, and occur as a result of mutations in the gene involved in synthesizing hemoglobin chains. By now more than 1000 defects in hemoglobin chains are d
Externí odkaz:
https://doaj.org/article/057d81f7d64b4ac9a8beecd74d553c80
Autor:
Anupa Pillai, Tushar Kanti Biswas
Publikováno v:
MGM Journal of Medical Sciences, Vol 6, Iss 3, Pp 148-151 (2019)
A 62-year-old woman with no comorbidity presented with dyspnea since 2 months and fatigue since 1 month. She was having severe anemia with hepatosplenomegaly and icterus. Anemia due to blood loss was ruled out. With a history of blood transfusions an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::282bcc389ad09def6b89e89c620901c7
http://www.mgmjms.com/article.asp?issn=2347-7946
http://www.mgmjms.com/article.asp?issn=2347-7946