Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Pooja Dabke"'
Autor:
Roshan B. Colah, Dipti Upadhye, Pratibha Sawant, Dipty Jain, Pooja Dabke, Ajit Gorakshakar, Yazdi M. Italia, Harshada Kangane, Stacy Colaco, Kanjaksha Ghosh, Khushnooma Italia, Anita Nadkarni
Publikováno v:
Clinica Chimica Acta. 431:46-51
Background Co-inheritance of structural hemoglobin variants like HbS, HbD Punjab and HbE can lead to a variable clinical presentation and only few cases have been described so far in the Indian population. Methods We present the varied clinical and h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::052f9f0ad287d0701521397710adffde
https://doi.org/10.1016/j.cca.2014.01.028
https://doi.org/10.1016/j.cca.2014.01.028
Publikováno v:
Blood Cells, Molecules, and Diseases. 50:156-160
The clinical and hematological course of β thalassemia intermedia is influenced by a number of genetic factors which play a role in increasing fetal haemoglobin levels. Several polymorphisms located in the promoters of β and γ globin gene are invo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e00127b8fffe6350c7d2c864b7c3b127
https://doi.org/10.1016/j.bcmd.2012.11.003
https://doi.org/10.1016/j.bcmd.2012.11.003
Autor:
Kanjaksha Ghosh, Pooja Dabke, Pratibha Sawant, Khushnooma Italia, Anita Nadkarni, Roshan B. Colah
Publikováno v:
Hemoglobin. 40(5)
Hb E [β26(B8)Glu→Lys; HBB: c.79G A]-β-thalassemia (β-thal) has an extremely variable clinical presentation. We report the clinical features of these patients from five Indian states together with their hematological and molecular characteristics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08ee91a0bff3f3e444eb398aa92a12bd
https://pubmed.ncbi.nlm.nih.gov/27623935
https://pubmed.ncbi.nlm.nih.gov/27623935
Publikováno v:
International journal of laboratory hematology. 37(6)
Summary Background The term thalassemia intermedia describe a form of thalassemia of intermediate severity, between the major transfusion-dependent forms of the disease and the symptomless carrier states. The phenotypic diversity of β-thalassemia re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5b8b555470d293a9c188b54e6dff480
https://pubmed.ncbi.nlm.nih.gov/26226914
https://pubmed.ncbi.nlm.nih.gov/26226914
Publikováno v:
Hematology (Amsterdam, Netherlands). 19(7)
Gilbert syndrome is characterized by mild unconjugated hyperbilirubinemia. The high levels of bilirubin could be related to the co-inheritance of Gilbert syndrome determined either by mutations of the coding region or by variation in the (TA)n motifs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb2a1a6c26533cad3f3a1d8c3d0e3940
https://pubmed.ncbi.nlm.nih.gov/24620945
https://pubmed.ncbi.nlm.nih.gov/24620945
Publikováno v:
Blood cells, moleculesdiseases. 52(4)
Sickle cell anemia is common in the Middle East and India where the HbS gene is sometimes associated with the Arab-Indian (AI) β-globin gene (HBB) cluster haplotype. In this haplotype of sickle cell anemia, fetal hemoglobin (HbF) levels are 3-4 fold
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b02f9f97d087b96d43462b98b8c2414
https://pubmed.ncbi.nlm.nih.gov/23465615
https://pubmed.ncbi.nlm.nih.gov/23465615
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases
Mediterranean Journal of Hematology and Infectious Diseases, Vol 5, Iss 1, Pp e2013012-e2013012 (2013)
Mediterranean Journal of Hematology and Infectious Diseases, Vol 5, Iss 1, Pp e2013012-e2013012 (2013)
The clinical presentation of b-thalassemia intermedia phenotypes are influenced by many factors .The persistence of fetal hemoglobin and several polymorphisms located in the promoters of g- and b-globin genes are some of them .The aim of this study w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::175525090920da2adf7f24e0024be420
https://doi.org/10.4084/mjhid.2013.012
https://doi.org/10.4084/mjhid.2013.012