Zobrazeno 1 - 10
of 126
pro vyhledávání: '"abnormal haemoglobin"'
Publikováno v:
Advances in Human Biology, Vol 13, Iss 4, Pp 313-321 (2023)
Thalassaemia constitutes an especially prevalent human monogenic illness caused by a lack of synthesis of the α- or β-globin chains. The clinical impact of β-thalassaemia is worse since it consists of the same pair gene configuration, thalassaemia
Externí odkaz:
https://doaj.org/article/8fb0b2c4e03b4ec0b4482af66e2281a3
Publikováno v:
Electronic Physician, Vol 9, Iss 3, Pp 4003-4008 (2017)
Thalassemia is a genetic disorder that involves abnormal haemoglobin formation. The two main categories of thalassemia are alpha and beta thalassemia that are then divided into further subcategories. While some mild forms of thalassemia might even
Externí odkaz:
https://doaj.org/article/d73e85a3e3bf41eb97924137746a4208
Autor:
Ishrat H Dar, Showkat H Dar, Muqtasid A Kamili, Mohammad I Quadri, Hardeep S Wazir, Aijaz A Bhat
Publikováno v:
Saudi Journal of Medicine and Medical Sciences, Vol 3, Iss 1, Pp 64-67 (2015)
Familial erythrocytosis is a heterogeneous group of hereditary conditions with an increased total red blood cell volume. The disease occurs in a familial pattern and follows a relatively benign course. The absence of leukocytosis and thrombocytosis d
Externí odkaz:
https://doaj.org/article/2458647c2b0a4b7cbc1b0f1245f27122
Autor:
Anurag Choubisa, Shanti Lal Choubisa
Publikováno v:
Proceedings of the Indian National Science Academy. 87:433-445
In India, Rajasthan is the largest state having two distinct environments separated by presence of Aravali Mountains. One is desert, located in the west region and other is humid in the east region where malaria is endemic. In Rajasthan, various inhe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d982c9b0a2f83fb4e4785f08c9e5ae8f
https://doi.org/10.1007/s43538-021-00045-2
https://doi.org/10.1007/s43538-021-00045-2
Akademický článek
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Autor:
Shubhi Saxena, Richa Jain
Publikováno v:
Tropical Journal of Pathology and Microbiology. 5:856-862
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dca83d71cbd6c4a3da6c96d17fb7f74a
https://doi.org/10.17511/jopm.2019.i11.04
https://doi.org/10.17511/jopm.2019.i11.04
Autor:
Richa Jain, Shubhi Saxena
Publikováno v:
Tropical Journal of Pathology and Microbiology. 5:925-933
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eeb056c5f19e56fbe167a6e70b2aad71
https://doi.org/10.17511/jopm.2019.i11.15
https://doi.org/10.17511/jopm.2019.i11.15
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 8, Iss 3, Pp 344-346 (2008)
The haematological and clinical findings of a three year old Omani girl, phenotypically compound heterozygote for Hb S and Hb S Oman, are presented, further substantiated by family studies. The necessity of reviewing cases with sickle cell haemoglobi
Externí odkaz:
https://doaj.org/article/83c78cbfe03e49c091a24ae011e5876c
Publikováno v:
Electronic Physician, Vol 9, Iss 3, Pp 4003-4008 (2017)
Electronic Physician
Electronic Physician
Thalassemia is a genetic disorder that involves abnormal haemoglobin formation. The two main categories of thalassemia are alpha and beta thalassemia that are then divided into further subcategories. While some mild forms of thalassemia might even go
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26725d4b4e09971e6af9a2580e27c01b
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5407235/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5407235/
Autor:
Jie Zhang, Yang Yang, Jie Su, Dongmei Li, Xiaohong Zeng, Peng Li, Yuanlong Yan, Hong Chen, Baosheng Zhu
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-8 (2019)
Scientific Reports
Scientific Reports
Abnormal haemoglobin (Hb) variants result in the most commonly inherited disorders in humans worldwide. In this study, we investigated the molecular epidemiology characteristics of Hb variants, along with associated structural and functional predicti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fc3800565277c15f5a319c0fee278ed
https://doi.org/10.1038/s41598-019-44793-0
https://doi.org/10.1038/s41598-019-44793-0