Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Benjamin, Augustine"'
Autor:
Ebele I Uche, Nwakaego E Chukwukaodinaka, Akinsegun A Akinbami, Oluwatosin I Adeyemi, Aderonke O Hassan, Rafah A Bamiro, Ismaila Nda Ibrahim, Aisha M Suleiman, Benjamin Augustine, Doris Chinyelu Anaduaka
Publikováno v:
Nigerian Postgraduate Medical Journal, Vol 29, Iss 3, Pp 228-235 (2022)
Background: Hepatitis B virus (HBV) infection is one of the public health diseases causing global health problems. It is a leading cause of cirrhosis and hepatocellular carcinoma. Blood transfusion is a major route of its transmission and screening o
Externí odkaz:
https://doaj.org/article/bccd2b7ab6d245d6975a1f89ef5ef53d
Autor:
Ebele Uche, Festus Olowoselu, Benjamin Augustine, Aisha Suleiman, Ayobami Ismail, Esther Oluwole, Akinsegun Akinbami, Lawretta Onwah
Publikováno v:
Journal of Applied Hematology, Vol 11, Iss 2, Pp 59-63 (2020)
INTRODUCTION: Sickle cell anemia is associated with intense oxidative stress, and optimal antioxidant levels are essential to prevent continuous oxidant tissue damage. The role of oxidant damage to red blood cells in sickle cell anemia (SCA) has been
Externí odkaz:
https://doaj.org/article/f8583dc90c674211bd8cb3bb59a242d8
Autor:
Akinsegun Akinbami, Ola Bola, Ebele Uche, Mulikat Badiru, Olusola Olowoselu, Aishatu Maude Suleiman, Benjamin Augustine
Publikováno v:
Journal of Applied Hematology, Vol 10, Iss 3, Pp 94-98 (2019)
BACKGROUND: Prolonged use of pentazocine in sickle cell disease (SCD) because of chronic pain may result in mental dependence (addiction) and/or physical dependence leading to withdrawal symptoms on suddenly stopping its use. This study was aimed at
Externí odkaz:
https://doaj.org/article/4b812653b10e46aa999f69570fdc9978
Autor:
Benjamin, Augustine1, Adeshola, Adebayo2, Fatima, Abdulrahman2, John, Johnson2, Akintunde, Akinrinmade2, Mohammed, Ibrahim3, Benedict, Amalimeh4, Jatau, Abdullahi2, Haruna, Muktar1
Publikováno v:
Egyptian Journal of Haematology. Jul-Sep2022, Vol. 47 Issue 3, p227-231. 5p.
Autor:
Ebele Uche, Olufunto Kalejaiye, Festus Olowoselu, Timothy Ekwere, Rafatu Bamiro, Abdulateef Kareem, Benjamin Augustine, Odebiyi Hassan, Abdulhafeez Balogun, Akinsegun Akinbami
Publikováno v:
International Journal of Scientific Reports. 9:5-10
Background: In sickle cell anaemia, there is an ever-present risk for haemostatic abnormalities which may result in reduced levels of naturally occurring coagulation inhibitors. Protein S is a Vitamin-K dependent, γ-carboxy glutamic acid-containing
Autor:
Muhammed Ahmed, Benjamin Augustine, Messi Matthew, Mudi Awaisu, Abdullahi Sudi, Kolapo B Hamza, Ahmad Bello, Hussaini Yusuf Maitama
Publikováno v:
Nigerian Journal of Surgery, Vol 23, Iss 1, Pp 15-19 (2017)
Objectives: The objective of this study was to determine the nuances of management, prognostic factors, and outcome of ischemic priapism in patients seen at Ahmadu Bello University Teaching Hospital, Zaria, Nigeria. Patients and Methods: We retrospec
Externí odkaz:
https://doaj.org/article/72e7b153ac1b41da9f3ce92465f19910
Autor:
Akinsegun Abduljaleel Akinbami, Ebele Ifeyinwa Uche, Aishatu Maude Suleiman, Ann Abiola Ogbena, Festus Olusola Olowoselu, Benjamin Augustine, Mulikat Adesola Badiru, Rafat Abiodun Bamiro, Omolara Risqat Kamson
Publikováno v:
The Pan African Medical Journal, Vol 32, Iss 141 (2019)
INTRODUCTION: Sickle cell anaemia (SCA) is an inherited abnormality of haemoglobin associated with reduced life expectancy. Patients' complications include dyslipideamia. This study was aimed at determining the artherogenic index of plasma (AIP) in s
Externí odkaz:
https://doaj.org/article/d2925c6646d34da38c495923fb2378c6
Autor:
Benjamin Augustine, Saleh Musa, John Johnson, Hafiz Ashurah Sabiu, Yasmin Amira Mohammed, Ndagiyisa Josiah Nmadu, Umar Musa, Tidisha Innocent Lawrence, Mohammed Haruna Muktar
Publikováno v:
Jewel Journal of Medical Sciences. 2:213-222
Background: Plasma cell leukaemia (PCL) is a very rare and aggressive clinical variant of plasma cell dyscrasias with a dismal prognosis. Not less than 28% of patients die within one month after diagnosis. It could arise de novo and is known as prima
Autor:
Benjamin Augustine, Akinsegun Akinbami, Lawretta Onwah, Aisha Suleiman, Ayobami Ismail, Esther O. Oluwole, Ebele Uche, Festus Olusola Olowoselu
Publikováno v:
Journal of Applied Hematology, Vol 11, Iss 2, Pp 59-63 (2020)
INTRODUCTION: Sickle cell anemia is associated with intense oxidative stress, and optimal antioxidant levels are essential to prevent continuous oxidant tissue damage. The role of oxidant damage to red blood cells in sickle cell anemia (SCA) has been
Autor:
EbeleI Uche, NwakaegoE Chukwukaodinaka, AkinsegunA Akinbami, OluwatosinI Adeyemi, AderonkeO Hassan, RafahA Bamiro, IsmailaNda Ibrahim, AishaM Suleiman, Benjamin Augustine, DorisChinyelu Anaduaka
Publikováno v:
Nigerian Postgraduate Medical Journal. 29:228
Hepatitis B virus (HBV) infection is one of the public health diseases causing global health problems. It is a leading cause of cirrhosis and hepatocellular carcinoma. Blood transfusion is a major route of its transmission and screening of blood is s