Výsledky vyhledávání - "MESH: Hemoglobins, Abnormal"

Identification of α-globin chain variants: a report from Iran

Autor: Akbari, Mohammad Taghi, Hamid, Mohammad

Publikováno v: Archives of Iranian Medicine
Archives of Iranian Medicine, Academy of Medical Sciences of the I.R. Iran, 2012, 15 (9), pp.564-567

International audience; BACKGROUND: This study was carried out to identify molecular and hematological features of α- globin chain variants and to evaluate their effects on the clinical and hematological characteristics in Iranian individuals suspec

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::1ab8a8e9cabfaab6981aeb3767fbdf95
https://pubmed.ncbi.nlm.nih.gov/22924376

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Identification of rare hemoglobin variant (Hb Fairfax) causing dominant β-thalassemia phenotype in an Iranian family

Autor: Mohammad Esmaeil Akbari, Mina Izadyar, Mohammad Hamid

Publikováno v: Annals of Hematology
Annals of Hematology, Springer Verlag, 2011, 90 (3), pp.349-51. ⟨10.1007/s00277-010-1003-4⟩

Dear Editor, More than 900 hemoglobin (Hb) variants have been reported, and most variants are caused by mutations in the αor β-globin gene clusters [1]. Clinically, most of hemoglobin variants are asymptomatic, but some variants are unstable, with

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6807f029fdd704f4bb8ff40f2496e895
https://hal-riip.archives-ouvertes.fr/pasteur-00750569/file/fulltext.pdf

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First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia with delta globin CD12 {Asn-->Lys (AAT-->AAA)}HbA₂-NYU in Iran

Autor: Amirian, Azam, Karimipoor, Morteza, Jafarinejad, Masoumeh, Taghavi, Maryam, Kordafshari, Alireza, Fathi Azar, Samaneh, Mohammadi, Malihe Sadat, Zeinali, Sirous

Publikováno v: Archives of Iranian Medicine
Archives of Iranian Medicine, Academy of Medical Sciences of the I.R. Iran, 2011, 14 (1), pp.8-11

International audience; BACKGROUND: Co-inheritance of β- and δ-globin mutations in Iran is not uncommon. This situation may interfere with correct diagnosis and genetic counseling of α- and β-thalassemia in screening programs. Here we report the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::13e5d7c60e25de31dba3924e51147df5
https://hal-riip.archives-ouvertes.fr/pasteur-00829009/document

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