Results 111 to 120 of about 578,117 (273)
A SAFE AND RUNTIME MULTI-KEYWORD RANKED SEARCH FOR ENCRYPTED INFORMATION OVER CLOUD DATA
openalex +1 more source
End-to-end Keyword Spotting using Xception-1d
Juan Gómez‐Sanchís +5 more
openalex +1 more source
An empirical study on website usability elements and how they affect search engine optimisation
The primary objective of this research project was to identify and investigate the website usability attributes which are in contradiction with search engine optimisation elements.
Eugene B. Visser, Melius Weideman
doaj
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken +4 more
wiley +1 more source
مشروع توشيهيكو إيزوتسو (Toshihiko Izutsu) في تأصيل علم دلالة القرآن
The aim of this article is to touch the methodological foundations which were put by the researcher “Toshihiko Izutsu” on semantics of the Qur’an, and how he described the radical change of the overall conceptual structure of the arabic lexicon applying ...
خديجة حاج مدني
doaj
ABSTRACT We examined the relationship between adverse childhood experiences (ACEs) and epigenetic age acceleration (EAA) in adulthood as measured by second and third generation epigenetic clocks by performing a systematic review of the literature. The electronic databases MEDLINE and EMBASE were searched on 17 July 2023.
Matthew Green +2 more
wiley +1 more source
ABSTRACT Women with the FMR1 premutation (PM) are at increased risk for fragile X‐associated conditions (FXPAC), including cognitive and psychiatric features collectively termed fragile X‐associated neuropsychiatric disorders (FXAND). This study is the first to systematically investigate cognitive and psychiatric features in Italian female premutation ...
Federica Alice Maria Montanaro +5 more
wiley +1 more source
Genetic and Phenotypic Features of the Five Known Polyaminopathies: A Critical Narrative Review
ABSTRACT Polyaminopathies are a recently described family of rare genetic neurodevelopmental disorders. Polyaminopathies disrupt the biosynthesis of the primary polyamines: putrescine, spermidine, and spermine. Snyder–Robinson syndrome results from hemizygous loss‐of‐function variants in the spermine synthase (SMS) gene, resulting in decreased or ...
Elizabeth A. VanSickle +26 more
wiley +1 more source

