Accès ouvert
2025
article
OpenAlex
Khalid Gaffer Mohamed, Amer Almarabheh, Aya M. Haiba, Leena Mohamed Khalid et autres
BACKGROUND: Person-centered care (PCC) emphasizes a collaborative, empathetic approach to healthcare, which marks a significant shift from the traditional, hierarchical biomedical model. The Patient-Practitioner Orientation Scale (PPOS) is a validated tool used to assess attitudes toward PCC. However, no prior studies have …
bh, Soudan
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Accès ouvert
2025
article
OpenAlex
Sara Emad, Sara Elawad, Shaima Omer Mohamed Elawad, Ahmed Balla M. Ahmed et autres
Depression is common among individuals with diabetes mellitus, yet many cases go undiagnosed. It is linked to poorer treatment outcomes. However, data from developing countries remains limited. This study aimed to assess the prevalence and severity of depression among diabetic patients in …
Soudan
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Sara Emad, Aziz M. Alduwais Abdul, Mohamed Mahmoud
The study aims to predict domestic consumption and the production of three meat species (cattle, goats, and sheep) between 2022 and 2030. All series data in addition income per capita as exogenous variable are stationary at the first difference. So vector autoregressive …
sa
(code pays fourni par la source)
Accès ouvert
2023
article
OpenAlex
Lina Hemmeda, Esraa S. A. Alfadul, Mohamed Satti, Alaa S. Ahmed et autres
One of the major challenges that stem cell transplantation faces is a lack of donors due to a lack of knowledge and awareness of the importance of stem cell transplantation, this implies that health care providers should arm themselves with sufficient knowledge …
Soudan, in, us, gb, Sénégal
(code pays fourni par la source)
Accès ouvert
2023
article
OpenAlex
Ashraf Yahia, Ahlam A. Hamed, Inaam N. Mohamed, Maha A. Elseed et autres
Hereditary spinocerebellar degenerations (SCDs) is an umbrella term that covers a group of monogenic conditions that share common pathogenic mechanisms and include hereditary spastic paraplegia (HSP), cerebellar ataxia, and spinocerebellar ataxia. They are often complicated with axonal neuropathy and/or intellectual impairment and …
fr, se, Soudan, sa, Afrique du Sud, qa, us, gb, jp
(code pays fourni par la source)
Accès ouvert
2022
article
OpenAlex
Elfatih A. Hasabo, Ghassan E. Ahmed, Raed M. Alkhalifa, Mai D. Mahmoud et autres
INTRODUCTION: Statistics helps medical students understand research. Without understanding statistics, students can't choose the proper analysis in their research. We aimed to assess the attitude toward statistics, usage of statical software and associated factors for using statistical analysis software in Sudan. METHOD: …
Soudan, gb
(code pays fourni par la source)
Accès ouvert
2022
preprint
OpenAlex
Giovanni Stévanin, Ahlam A. Hamed, Inaam N. Mohamed, Maha A. Elseed et autres
Abstract Hereditary spinocerebellar degenerative disorders (SCDs) is an umbrella term that covers a group of monogenic conditions that share common pathogenic mechanisms and include spastic paraplegia, spastic ataxia, cerebellar ataxia, and spinocerebellar ataxia. They are often complicated with axonal neuropathy and/or intellectual …
fr, Soudan, sa, Afrique du Sud, us, qa, se, gb, ru
(code pays fourni par la source)
Accès ouvert
2022
article
OpenAlex
Fahimeh Rezazadeh, Negin Esnaashari, Azita Azad, Sara Emad
BACKGROUND: Temporomandibular disorder (TMD) is the main cause of non-dental pain in orofacial area. The most common symptoms of TMD are joint pain, joint sound and limitation of jaw function. Botulinum toxin (BTX) injection is considered a potential treatment for TMD due …
ir
(code pays fourni par la source)
2022
article
OpenAlex
Ashraf Yahia, Ikhlas Ben Ayed, Ahlam A. Hamed, Inaam N. Mohammed et autres
BACKGROUND: Intellectual disability is a form of neurodevelopmental disorders that begin in childhood and is characterized by substantial intellectual difficulties as well as difficulties in conceptual, social, and practical areas of living. Several genetic and nongenetic factors contribute to its development; however, …
fr, Soudan, Tunisie, us, sa
(code pays fourni par la source)
Accès ouvert
2021
article
OpenAlex
Ashraf Yahia, Liena E. O. Elsayed, Rémi Valter, Ahlam A. Hamed et autres
Introduction: Hereditary spastic paraplegia is a clinically and genetically heterogeneous neurological entity that includes more than 80 disorders which share lower limb spasticity as a common feature. Abnormalities in multiple cellular processes are implicated in their pathogenesis, including lipid metabolism; but still …
fr, Soudan, sa, de, ie, jp
(code pays fourni par la source)
Accès ouvert
2021
article
OpenAlex
Ashraf Yahia, Zhefan Stephen Chen, Ammar Ahmed, Sara Emad et autres
BACKGROUND: CCDC88C is a ubiquitously expressed protein with multiple functions, including roles in cell polarity and the development of dendrites in the nervous system. Bi-allelic mutations in the CCDC88C gene cause autosomal recessive congenital hydrocephalus (OMIM #236600). Studies recently linked heterozygous mutations …
fr, Soudan, hk, sa
(code pays fourni par la source)
Accès ouvert
2020
preprint
OpenAlex
Ashraf Yahia, Ahlam A. Hamed, Fatima Abozar, Rawaa Adil et autres
Abstract BackgroundAutosomal recessive intellectual disabilities, syndromic and non-syndromic, are of specific importance in consanguineous communities. High throughput sequencing technologies have enhanced diagnosing the Mendelian forms of intellectual disability. Mental retardation 36 and 38 are emerging clinical entities with variable presentations that extend …
Soudan, fr
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