Effect of Copper and Zinc Ions on Biochemical and Molecular Characteristics of Calcium Oxalate Renal Stones: a Controlled Clinical Study

SAY Taha, AA Shokeir, WI Mortada, A Awadalla… - … Trace Element Research, 2024 - Springer
Contradictory results are existed in the literature regarding the impact of trace elements on
the pathogenesis of calcium oxalate (CaOx) stone patients. Therefore, the aim of our study …

[HTML][HTML] Neonatal hypocalcemia and its relation to vitamin D and calcium supplementation

…, WS Mohammed, OM Zaki, SA Taha - Saudi medical …, 2018 - ncbi.nlm.nih.gov
Objectives: To assess the prevalence of hypocalcemia in outpatient clinic neonates and its
relation to vitamin D and calcium supplementation. Methods: This cross-sectional analytical …

Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations

…, ESA Alfadul, M Fadul, KF Ali, SOMA Taha… - European Journal of …, 2023 - nature.com
Hereditary spinocerebellar degenerations (SCDs) is an umbrella term that covers a group of
monogenic conditions that share common pathogenic mechanisms and include hereditary …

[HTML][HTML] Congenital brain malformations in Sudanese children: an outpatient-based study

…, AA Hamed, MO Babiker, SO Taha - Sudanese Journal of …, 2018 - ncbi.nlm.nih.gov
Congenital brain malformations (CBMs) are a heterogeneous group characterised by
abnormal structure of the developing brain. Their aetiology includes in-utero infections, …

Intra-familial phenotypic heterogeneity in a Sudanese family with DARS2-related leukoencephalopathy, brainstem and spinal cord involvement and lactate elevation …

…, M Amin, M Koko, R Abubakr, R Idris, SOMA Taha… - BMC neurology, 2018 - Springer
Background Leukoencephalopathy with brainstem and spinal cord involvement and lactate
elevation (LBSL, OMIM #611105) is a genetic disease of the central nervous system …

A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report

…, AE Ahmed, S Emad, R Adil, R Abubaker, SOMA Taha… - BMC neurology, 2021 - Springer
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 …

MDS-related anemia is associated with impaired quality of life but improvement is not always achieved by increased hemoglobin level

Y Haring, N Goldschmidt, S Taha, G Stemer… - Journal of Clinical …, 2023 - mdpi.com
Quality of life is impaired in MDS, but the role of hemoglobin level is unclear. To study the Hb–QoL
correlation at diagnosis and 1 year later, patients filled out the EQ-5D questionnaire, …

Religious Tourists' Satisfaction with Services and Their Impacts on Spirituality in the Post-COVID-19 Era

TH Hassan, AH Abdou, S Taha, MA Abdelmoaty… - Sustainability, 2022 - mdpi.com
Islamic pilgrimage has social, political, and economic benefits, but there are major challenges
in the management of large numbers of groups at one time. This spiritually healing …

THE EFFECT OF APPLYING GEOFENCING TECHNOLOGY ON THE EGYPTIAN CUSTOMERS'PURCHASING INTENTION TO TOUR SERVICES

S Taha, G El-Mawardy - مجلة کلية السياحة والفنادق. جامعة …, 2022‎ - mkaf.journals.ekb.eg
Mobile-based marketing has been increasingly adopted by many enterprises’ marketing
campaigns with the dominance of smartphone usage all over the world. Geofencing technology …

Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degeneration

…, A Elbashier, E Alfadul, M Fadul, K Ali, S Taha… - 2022 - researchsquare.com
Hereditary spinocerebellar degenerative disorders (SCDs) is an umbrella term that covers a
group of monogenic conditions that share common pathogenic mechanisms and include …