Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Ibrahim Kalle Kwaifa"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Abstract Background Defective synthesis of the α-globin chain due to mutations in the alpha-globin genes and/or its regulatory elements leads to alpha thalassaemia syndrome. Complete deletion of the 4 alpha-globin genes results in the most severe ph
Externí odkaz:
https://doaj.org/article/c057a93b27b24f90b2d2112587225a37
Publikováno v:
Biomolecules, Vol 10, Iss 2, p 291 (2020)
Obesity is characterized by the excessive deposition of fat that may interfere with the normal metabolic process of the body. It is a chronic condition associated with various metabolic syndromes, whose prevalence is grossly increasing, and affects b
Externí odkaz:
https://doaj.org/article/2b1227018cdc47dbae4defc4944e6090
Autor:
null Aliyu Garba Bashiru, null Abdulrahman Yakubu, null Ibrahim Kalle Kwaifa, null Hussaini Muhammad Alhassan, null Sirajo Bello Shittu, null Usman Abubakar, null Aliyu Bagudo Ibrahim, null Hauwa Ali Buhari, null Festus Uchechukwu Onuigwe, null Lukman Haruna
Publikováno v:
International Journal of Scholarly Research and Reviews. 2:035-044
Anemia is a serious health condition in Sub Saharan Africa (SSA). The region is vulnerable to multiple underlying causes of anaemia that are many and varied. It affects children under five years, nonpregnant women, pregnant women and the elderly. Man
Autor:
Sani Lawal Sani, Muhammad Sani Kasimu, Hauwa Buhari Ali, Ibrahim Aliyu Bagudo, Festus Ouigwe, Ibrahim Kalle Kwaifa, Aliyu Garba, Abdulrahman Yakubu, Yazid Bello, Lukman Haruna
Publikováno v:
East African Journal of Health and Science. 6:133-153
Myeloproliferative disorders (MPD) are clonal hematopoietic disorders characterized by abnormal clone expansion of haematological progenitor cells, which can lead to thrombosis, bleeding, and/or transformation to leukaemia. Chronic myelogenous leukae
Publikováno v:
International Blood Research & Reviews. 14:40-49
Urinary schistosomiasis or Bilharzia caused by fluke worm Schistosoma haematobium (S. haematobium) is one of the seventeen (17) neglected tropical diseases associated with serious health problems and morbidities. It affects over 200 million people gl
Autor:
Kokila Vani Perumal, Hasnah Bahari, NorShafarina Shari, Kasturi Kanniappan, Khairul Kamilah Abdul Kadir, Zunoliza Abdullah, Mohd Radzi Ahmad, Ibrahim Kalle Kwaifa, Siti Hadizah Jumidil, Azrina Zainal Abidin, Sabariah Md Noor, Yoke Keong Yong, Santhra Segaran Balan
Publikováno v:
Malaysian Journal of Medicine and Health Sciences. 18:55-63
Introduction: The incidence and complications of hyperlipidemia associated co-morbidities and mortalities are grossly increasing globally. Intervention with natural products preparation has been identified as an alternative for the management of hype
Autor:
Azrina Zainal Abidin, Santhra Segaran Balan, Kokila Vani Perumal, Ibrahim Kalle Kwaifa, Hasnah Bahari, Maizaton Atmadini Abdullah, Azmiza Syawani Jasni, Nurul Husna Shafie
Publikováno v:
Sains Malaysiana. 50:3045-3057
Obesity has been considered as a great public health concern, that has spread in both economic and poor resources countries. This study aimed to investigate the effect of Elateriospermum tapos supplementation on the male offspring of female obesity-i
Autor:
Ibrahim Kalle Kwaifa
Publikováno v:
Anticoagulation-Current Perspectives
Anticoagulants are chemical substances that prevent coagulation or prolong the clotting time by suppressing the functions or synthesis of coagulation factors in the blood. Anticoagulation mechanisms are essential in controlling the formation of a blo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0fd236b624f03ea3eefcc879d790527
https://mts.intechopen.com/articles/show/title/anticoagulants-and-hypercoagulability
https://mts.intechopen.com/articles/show/title/anticoagulants-and-hypercoagulability
Autor:
Santhra Segaran Balan, Sabariah Md Noor, Kokila Vani Perumal, Kasturi Kanniappan, Ibrahim Kalle Kwaifa, Hasnah Bahari, Mohd Radzi Ahmad, Khairul Kamilah Abdul Kadir, Yong Keong, Azrina Zainal Abidin, Zunoliza Abdullah, Norshafarina Shari
Publikováno v:
Proceedings of The 1st International Electronic Conference on Nutrients - Nutritional and Microbiota Effects on Chronic Disease.
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Background Defective synthesis of the α-globin chain due to mutations in the alpha-globin genes and/or its regulatory elements leads to alpha thalassaemia syndrome. Complete deletion of the 4 alpha-globin genes results in the most severe phenotype k