Accès ouvert
2026
review
OpenAlex
Abdulmajeed Albalawi, Mohammed N. Almohammadi, Shaker A. Alsharif, Maha Alotaibi et autres
INTRODUCTION Low bone mineral density (BMD), including osteopenia and osteoporosis, is a frequent complication in patients with chronic lung diseases, yet global estimates for certain populations remain variable.Various studies have reported a high clinical burden of bone disease in patients with interstitial …
sa
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Accès ouvert
2026
article
OpenAlex
Jameel Fakeeha, Maha Alotaibi, Ibrahim F Alshugair, Nouf Altwaijri
3M syndrome is a rarely inherited autosomal recessive disorder caused by mutations in cullin-7 (CUL7), obscurin-like 1 (OBSL1), and coiled-coil domain containing protein 8 (CCDC8). It is associated with multiple dysmorphic features, including characteristic facial dysmorphism (a face that is triangular, full …
sa
(code pays fourni par la source)
Accès ouvert
2025
dissertation
OpenAlex
Maha Alotaibi
Ischemic Heart Disease (IHD) is known as a leading cause of death and disability adjusted life years in recent decades, especially in Saudi Arabia. Higher levels of physical activity (PA) and perceived social support (PSS) were positively associated with improved outcomes like …
Accès ouvert
2025
dissertation
OpenAlex
Maha Alotaibi
Ischemic Heart Disease (IHD) is known as a leading cause of death and disability adjusted life years in recent decades, especially in Saudi Arabia. Higher levels of physical activity (PA) and perceived social support (PSS) were positively associated with improved outcomes like …
2025
conference-abstract
OpenAlex
Maha Alotaibi, Mia Cajita, Susan L. Dunn
Background: Physical activity (PA) has been shown to improve cardiovascular outcomes, including health-related quality of life (HRQoL), in patients with acute coronary syndromes (ACS). Furthermore, studies have shown the impact of perceived social support (PSS) in enhancing PA levels and, as a …
us
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Accès ouvert
2025
article
OpenAlex
Khadijah Bakur, Halima Hamid, Bader Alhaddad, Majid Alfadhel et autres
BACKGROUND: Clinical exome and genome sequencing has transformed the diagnostic workup of patients with genetic disorders. The extensive body of evidence supporting the application of this clinical genomics approach in pediatric patients stands in stark contrast to the relative paucity of evidence …
sa, us, Soudan, ca
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Accès ouvert
2025
article
OpenAlex
Areej Hassan Alatawi, Omamah Alshehri, Fuad Al Mutairi, Norah Alsaleh et autres
SLC25A42 encodes a mitochondrial carrier that is responsible for the import of CoA into mitochondria. Biallelic pathogenic variants in SLC25A42 have been associated with a recently described mitochondrial disorder characterized by encephalomyopathy with variable severity. To date, 24 affected individuals from 16 …
sa, us
(code pays fourni par la source)
2025
article
OpenAlex
Maha Alotaibi, Mia Cajita, Nathan Tintle, Holli A. DeVon et autres
BACKGROUND: Associations among perceived social support (PSS), physical activity (PA), and health-related quality of life (HRQoL) in individuals with ischemic heart disease (IHD) are well established. However, little is known about these associationsin patients with IHD experiencing hopelessness. OBJECTIVE: The objective of …
us, gb
(code pays fourni par la source)
2025
article
OpenAlex
Sahal Alotaibi, Maha Alotaibi, Hadiya Nassar Alrashedi, Huda Ali S Alasmari et autres
sa, Égypte, ae
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Accès ouvert
2024
article
OpenAlex
Maha Alotaibi
Introduction: Genetics’ integration with society sparks a multifaceted exploration in medicine, ethics, and psychology. This survey probes parental perspectives on childhood genetic disorders, aiming to gauge their understanding, attitudes, and implications. It seeks to inform healthcare, counseling, and policy endeavors by uncovering …
sa
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Yaseen M. Arabi, Hasan M. Al‐Dorzi, Omar Aldibaasi, Musharaf Sadat et autres
BACKGROUND: The optimal amount and timing of protein intake in critically ill patients are unknown. REPLENISH (Replacing Protein via Enteral Nutrition in a Stepwise Approach in Critically Ill Patients) trial evaluates whether supplemental enteral protein added to standard enteral nutrition to achieve …
sa, kw, Égypte, ee, be, dk, us
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Accès ouvert
2024
article
OpenAlex
Valentina Cetica, Tiziana Pisano, Gaëtan Lesca, Dana Marafi et autres
OBJECTIVE: YWHAG variant alleles have been associated with a rare disease trait whose clinical synopsis includes an early onset epileptic encephalopathy with predominantly myoclonic seizures, developmental delay/intellectual disability, and facial dysmorphisms. Through description of a large cohort, which doubles the number of …
it, fr, us, kw, hk, dk, gb, lt, sa, ca, nl, iq, tw
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