Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Maha Saleh"'
Physical activity and health-related quality of life among adults living in Jeddah city Saudi Arabia
Autor:
Ola Akram Abdulrashid, Hassan Bin Usman Shah, Wijdan Abdulkareem Baeshen, Sarah Mohammad Aljuaid, Enas Awad Alasmari, Rania Ali Baokbah, Reema Ali Baokbah, Nojoud Mohammed Alamoudi, Maha Saleh Alkhelewi, Amal Abdullah Turkistani, Ahmed Abdullah Alharbi, Abdulrehman Ahmed Alghamdi, Fawaz Alharthi, Mohammad Alcattan, Amnah Marwan Haikal
Publikováno v:
PeerJ, Vol 11, p e16059 (2023)
Background Physical activity can improve health-related quality of life (HRQoL) in adults. However, the effect of physical activity on quality of life is unclear among the Saudi adult population. The study aimed to determine the association between p
Externí odkaz:
https://doaj.org/article/695382bcf5b04a3084d9c26cca9381a3
Publikováno v:
Clinical Case Reports, Vol 11, Iss 8, Pp n/a-n/a (2023)
Key Clinical Message We present a patient with cri‐du‐chat syndrome secondary to a rare cytogenetic mechanism. Our patient was the product of a dichorionic diamniotic twin pregnancy initially flagged with soft markers on ultrasound and uninformat
Externí odkaz:
https://doaj.org/article/492af20b92af4423bd8edb1aad4dc8a4
Autor:
Talib Al Harthy, Samantha Colaiacovo, Robert J. Gratton, Kevin Coughlin, Victoria Mok Siu, Chitra Prasad, Charles Rupar, Maha Saleh
Publikováno v:
Clinical Case Reports, Vol 11, Iss 8, Pp n/a-n/a (2023)
Key Clinical Message Non‐immune hydrops is a prenatal finding which can occur due to an underlying genetic diagnosis such as common chromosomal aneuploidy (Trisomy 21, Turner syndrome etc.). It is extremely rare to have more than one genetic cause
Externí odkaz:
https://doaj.org/article/d72f48a772a84348a568b01ef9fcab4b
Publikováno v:
Clinical Case Reports, Vol 10, Iss 8, Pp n/a-n/a (2022)
Abstract Pathogenic variants in the BRCA1 and BRCA2 genes are associated with increased risk for breast and ovarian cancers. Concurrent mutations in both genes in the same individual are rare but pose specific challenges when identified, usually thro
Externí odkaz:
https://doaj.org/article/0d26aef6851043cdb90ec6a90f24f13d
Autor:
Maha Saleh, Samantha Colaiacovo, Melanie P. Napier, Asuri N. Prasad, C. Anthony Rupar, Chitra Prasad
Publikováno v:
Case Reports in Genetics, Vol 2022 (2022)
We describe the diagnostic odyssey of an eight-year-old female born to consanguineous parents. Our patient presented with global developmental delay, regression, microcephaly, spastic diplegia, and leukodystrophy confirmed on brain magnetic resonance
Externí odkaz:
https://doaj.org/article/552b48ccc969443b9db8207a45c133aa
Publikováno v:
Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Abstract This report suggests that self‐resolving oligohydramnios is an early sign of malfunctioning kidney in individuals with renal coloboma syndrome (RCS) and demonstrates how a genetic diagnosis can impact patient and fetal management as it out
Externí odkaz:
https://doaj.org/article/b66b7283a099403984eb3ec4b19457e3
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 15 (2021)
Attention deficit hyperactivity disorder (ADHD) is one of the most common neurodevelopmental disorders among children. Working memory deficits underlie many of the behavioural symptoms of ADHD. Alongside psychostimulant medications, strategies to imp
Externí odkaz:
https://doaj.org/article/f06d3359ccc04333953bbd653d9fedd7
Autor:
Maha Saleh Alrajhi, Bader Mohammed Alim, Sara Dokhayel Aldokhayel, Leena Mohammad Zeitouni, Layan Khalid Al Tawil, Farid A Alzahrani
Publikováno v:
Journal of Nature and Science of Medicine, Vol 2, Iss 4, Pp 220-225 (2019)
Introduction: Cotton buds are small plastic rods with cotton-covered tips. They have been widely misused since their development. Objectives: This study aims to determine the prevalence of cotton bud usage and examine patients' attitudes toward their
Externí odkaz:
https://doaj.org/article/8101cd3360e3463eba5e3e8a4a6325f6
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 11, Pp n/a-n/a (2020)
Abstract Background Ectrodactyly‐ectodermal dysplasia‐clefting syndrome 3 (EEC) is one of the six overlapping syndromes caused by mutations in the tumor protein p63 gene (TP63). EEC is suspected when patients have cleft hands or feet, polydactyly
Externí odkaz:
https://doaj.org/article/987c96a1f34042ce87929a5b50ae5770
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.