Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Abubaker A. Mohamedsharif"'
Autor:
Mohamed Abdualgafar Osman Mohamedsharif, Isra Bdraldein Salih Mohammed, Abubaker A. Mohamedsharif
Publikováno v:
Nursing Research and Practice, Vol 2024 (2024)
Introduction. The neonatal period is a crucial time for the survival, growth, and development of newborns. Despite advances in medical science, neonatal mortality rates remain a significant public health issue, and midwives play a critical role in re
Externí odkaz:
https://doaj.org/article/0ca10bdd2b4b4bdcaca260701f5ec537
Publikováno v:
Sudan Journal of Medical Sciences, Vol 17, Iss 4, Pp 556-564 (2022)
Abstract A 53-year-old female presented with itchiness in her back. She has a 5 years history of tightness of the skin on her face, neck, and torso bilaterally. She did not have other symptoms suggestive of systemic sclerosis (scleroderma), and her r
Externí odkaz:
https://doaj.org/article/06dc2f2c5ad54e2293cfcfabf895b2e6
Publikováno v:
Sudan Journal of Medical Sciences; Vol. 17 No. 4 (2022); 556–564
A 53-year-old female presented with itchiness in her back. She has a 5 years history of tightness of the skin on her face, neck, and torso bilaterally. She did not have other symptoms suggestive of systemic sclerosis (scleroderma), and her rheumatolo
Autor:
Yousuf Bakhit, Ina Schmitt, Ahlam Hamed, Etedal Ahmed A. Ibrahim, Inaam N. Mohamed, Sarah M. El-Sadig, Maha A. Elseed, Mohamed A. Alebeed, Mutaz T. Shaheen, Mohamed O. Ibrahim, Ali A. Elhassan, Khalid Eltom, Hiba A. Ali, Yousuf A. Ibrahim, Murad E. Almak, Rayan Abubaker, Mohamed Anwer Ahmed, Ahmed A. Abugrain, Salma M. Elrasheed, Mawia A. Omar, Mohamed A. Almahal, Abubaker A. MohamedSharif, Mohamed Y. Tahir, Sawazen M. Malik, Hazim S. Eldirdiri, Reem J. Khidir, Malaz T. Mohamed, Abdelmohaymin Abdalla, Farouk Yassen Omer, Liena E.O. Elsayed, Haydar El Hadi Babikir, Elfateh Abd-Allah Bukhari, Osheik Seidi, Ullrich Wüllner
Publikováno v:
Parkinsonism & related disorders 101, 6-8 (2022). doi:10.1016/j.parkreldis.2022.05.009
Several studies suggested a significant role of epigenetic changes, including alterations in miRNA, histone modifications, and DNA methylation of α-synuclein (SNCA) in Parkinson's disease (PD) pathogenicity. As of yet, only very few studies have bee
Autor:
Hajatmena A M Alkhedir, Abubaker A MohamedSharif, Isra Bdraldein Salih Mohammed, Inaam N Mohamed
ObjectivesThe main aim of the study is to classify patients with epilepsy using ILAE classification 2017, and to test whether it can like Sudan.MethodsThis is a descriptive, prospective cross sectional study, conducted in two main pediatric epilepsy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1edc265be7ff052c29aa7a31c0fd19fd
https://doi.org/10.1101/2022.10.14.22281100
https://doi.org/10.1101/2022.10.14.22281100
ObjectivesThe aim is to assess the knowledge, attitude and practice of the primary school teachers toward.MethodsA descriptive cross-sectional study was conducted among primary school teachers in Khartoum using self-administered, closed ended questio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfa35b6c450959dcd5e6406c741b93da
https://doi.org/10.1101/2022.10.10.22280849
https://doi.org/10.1101/2022.10.10.22280849
Autor:
DalyaMM Abdelmaged, Lamis AA KAddam, Haydar A Abdelrazig, Imad Fadl-Elmula, Abubaker A MohamedSharif, Hassan Elhag Hassan Abdalla, Isra Bdraldein Salih Mohammed, Amal M. Saeed
Background: Sickle cell disease is one of the common genetic diseases with an autosomal recessive inheritance. SCD have been acknowledge as an inflammatory condition with several indicators of an inflammatory response involving high level of white bl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b884b7a487959a383a0c1d2676a2797
https://doi.org/10.21203/rs.3.rs-2109339/v1
https://doi.org/10.21203/rs.3.rs-2109339/v1
Autor:
Yousuf Bakhit, Mohamed O. Ibrahim, Christelle Tesson, Ali A. Elhassan, Mohamed Anwer Ahmed, Mohamed A. Alebeed, Salma M. Elrasheed, Mawia A. Omar, Rayan Abubaker, Khalid Eltom, Mutaz T. Shaheen, Yousuf A. Ibrahim, Murad E. Almak, Hiba A. Ali, Ahmed A. Abugrain, Mohamed A. Almahal, Abubaker A. MohamedSharif, Mohamed Y. Tahir, Sawazen M. Malik, Hazim Eldirdiri Abdelrahman, Reem J. Khidir, Malaz T. Mohamed, Abdelmohaymin Abdalla, Liena E.O. Elsayed, Suzanne Lesage, Jean-Christophe Corvol, Osheik Seidi, Ullrich Wüllner
Publikováno v:
Parkinsonism & related disorders 111, 105401 (2023). doi:10.1016/j.parkreldis.2023.105401
PINK1 is the second most predominant gene associated with autosomal recessive Parkinson's disease. Homozygous mutations in this gene are associated with an early onset of symptoms. Bradykinesia, tremors, and rigidity are common features, while dyston
Autor:
Hajatmena A M Alkhedir, Abubaker A MohamedSharif, Isra Bdraldein Salih Mohammed, Inaam N Mohamed
Publikováno v:
Sudan Journal of Medical Sciences, Vol 18, Iss 4, Pp 488-497 (2023)
Abstract Background: The objective of this study is to utilize the ILAE 2017 to classify epilepsy patients and determine its applicability in Sudan. Methods: This study is a prospective, descriptive, cross-sectional research conducted in two pediatri
Externí odkaz:
https://doaj.org/article/f56ad796010c4e2a85fb421a829b8931