Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Eneh,Chizoma"'
Autor:
Odimegwu, Chioma Laura, Uwaezuoke, Samuel Nkachukwu, Chikani, Ugo N, Mbanefo, Ngozi Rita, Adiele, Ken Daberechi, Nwolisa, Charles Emeka, Eneh, Chizoma Ihuarula, Ndiokwelu, Chibuzo Obiora, Okpala, Somkenechi C, Ogbuka, Francis N, Odo, Kenneth E, Ohuche, Ijeoma Onyinyechukwu, Obiora-Izuka, Chinelo Elizabeth
Publikováno v:
Diabetes, Metabolic Syndrome & Obesity: Targets & Therapy; Sep2024, Vol. 17, p3557-3576, 20p
Autor:
Chime, Onyinye H1 (AUTHOR), Eneh, Chizoma I.2 (AUTHOR) zomafrank@yahoo.com, Asinobi, Isaac N2 (AUTHOR), Ekwochi, Uchenna2 (AUTHOR), Ndu, Ikenna Kingsley2 (AUTHOR), Nduagubam, Obinna C2 (AUTHOR), Amadi, Ogechukwu F2 (AUTHOR), Osuorah, Donatus Chidiebere3 (AUTHOR)
Publikováno v:
BMC Public Health. 4/11/2023, Vol. 23 Issue 1, p1-11. 11p. 1 Chart.
Publikováno v:
International Journal of TROPICAL DISEASE & Health. 44:23-30
Aim: To identify the quantity of haemoglobin (Hb) ‘S’(HbS), ‘A2’(HbA2), ‘F’(HbF) and other Hb phenotypes of sickle cell anaemia (SCA) children in Enugu Nigeria using High Performance Liquid Chromatography(HPLC). Introduction: The inherita
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14254a072e9b20358cbfd2cc05137aa4
https://doi.org/10.9734/ijtdh/2023/v44i71419
https://doi.org/10.9734/ijtdh/2023/v44i71419
Publikováno v:
International Journal of Current Research and Review. 15:01-09
Introduction: Parents with heterozygous sickle cell status [haemoglobin AS (HbAS) or sickle cell trait (SCT)] may produce sickle cell anaemia (SCA) patients. Proper diagnosis and correct reporting of sickle cell status is, therefore, necessary to gui
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b8b9c2aef53600294e4d6a6cec7d9ad
https://doi.org/10.31782/ijcrr.2023.15301
https://doi.org/10.31782/ijcrr.2023.15301
Publikováno v:
Journal of Advances in Medicine and Medical Research. :166-170
Aim: Highlight childhood Osteosarcoma as uncommon in a pre-adolescent female’s scapula. Presentation of Case: 9-year-old female with left scapular outgrowth, weight loss, paleness cachexia and axillary lymphadenopathy. Mass measured 27 by 53 cm, ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38327cf8d60e15ca8721e1e34f6fd42a
https://doi.org/10.9734/jammr/2022/v34i2231589
https://doi.org/10.9734/jammr/2022/v34i2231589
Akademický článek
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Autor:
Mbanefo,Ngozi R, Uwaezuoke,Samuel N, Eneh,Chizoma I, Odimegwu,Chioma L, Chikani,Ugo N, Muoneke,Uzoamaka V, Nwolisa,Charles E, Odo,Kenneth E, Ogbuka,Francis N, Akwue,Anthony T
Publikováno v:
International Journal of Nephrology and Renovascular Disease.
Ngozi R Mbanefo,1 Samuel N Uwaezuoke,1 Chizoma I Eneh,2 Chioma L Odimegwu,1 Ugo N Chikani,1 Uzoamaka V Muoneke,1 Charles E Nwolisa,3 Kenneth E Odo,1 Francis N Ogbuka,2 Anthony T Akwue4 1Department of Pediatrics, the University of Nigeria Teaching Hos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dovemedicalp::b1e96ffd77c00143d0591ef80bc132ed
https://www.dovepress.com/can-oral-zinc-supplementation-reduce-relapses-in-childhood-steroid-sen-peer-reviewed-fulltext-article-IJNRD
https://www.dovepress.com/can-oral-zinc-supplementation-reduce-relapses-in-childhood-steroid-sen-peer-reviewed-fulltext-article-IJNRD
Autor:
Eneh Chizoma Ihuarula
Publikováno v:
Journal of Advances in Medicine and Medical Research. :70-79
Background: Sickle cell anaemia, (SCA) the homozygous and most severe of the sickle cell diseases exerts adverse effects on growth and linear body proportions. In Nigeria, these changes in the lower extremity are scarcely documented. Objectives: To e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb5bae400ca3f28224bcf3a09d7c19d9
https://doi.org/10.9734/jammr/2020/v32i1630632
https://doi.org/10.9734/jammr/2020/v32i1630632
Autor:
Eneh Chizoma I
Publikováno v:
Indian Journal of Child Health. 7:324-327
Background: Sickle cell disease (SCD) is an autosomal recessive disorder with mutation in the hemoglobin gene. Sickle cell anemia (SCA), the homozygous state, has adverse effects. Community knowledge regarding personal sickle cell status and the inhe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::071eda02eaa6194fda1d06c389337ff9
https://doi.org/10.32677/ijch.2020.v07.i08.001
https://doi.org/10.32677/ijch.2020.v07.i08.001
Autor:
Uwaezuoke, Samuel N, Odimegwu, Chioma L, Mbanefo, Ngozi R, Eneh, Chizoma I, Arodiwe, Ijeoma O, Muoneke, Uzoamaka V, Ogbuka, Francis N, Ndiokwelu, Chibuzo O, Akwue, Anthony T
Publikováno v:
BMC Infectious Diseases; 3/14/2023, Vol. 23 Issue 1, p1-13, 13p