Adel Shalata
Overview
Explore the profile of Adel Shalata including associated specialties, affiliations and a list of published articles.
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Articles
41
Citations
400
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Recent Articles
1.
Shalata A, Saada A, Mahroum M, Hadid Y, Furman C, Shalata Z, et al.
Hum Genomics
. 2025 Feb;
19(1):21.
PMID: 40022150
Purpose: Sengers-syndrome (S.S) is a genetic disorder characterized by congenital cataracts, hypertrophic cardiomyopathy, skeletal myopathy and lactic acidosis. All reported cases were genetically caused by biallelic mutations in the AGK...
2.
Ruhrman Shahar N, Yagel D, Marek-Yagel D, Greenberg R, Isakov O, Naftali M, et al.
Circ Genom Precis Med
. 2025 Jan;
18(1):e004864.
PMID: 39866098
No abstract available.
3.
Tarabeih N, Kalinkovich A, Ashkenazi S, Shalata A, Livshits G
Biomolecules
. 2024 Nov;
14(11).
PMID: 39595602
In this study, we evaluated the contribution of the putative genetic factors into the established associations between selected circulating adipokine levels, body composition measurements, and low-back-pain-related disability scores (LBP_DS). A...
4.
Tarabeih N, Kalinkovich A, Ashkenazi S, Cherny S, Shalata A, Livshits G
Biomedicines
. 2024 May;
12(5).
PMID: 38791028
The associations of cardiovascular disease (CVD) with comorbidities and biochemical and body composition measurements are repeatedly described but have not been studied simultaneously. In the present cross-sectional study, information on...
5.
Foley A, Bolduc V, Guirguis F, Donkervoort S, Hu Y, Orbach R, et al.
medRxiv
. 2024 Apr;
PMID: 38585825
Collagen VI-related dystrophies (COL6-RDs) manifest with a spectrum of clinical phenotypes, ranging from Ullrich congenital muscular dystrophy (UCMD), presenting with prominent congenital symptoms and characterised by progressive muscle weakness, joint...
6.
Marom D, Mory A, Reytan-Miron S, Amir Y, Kurolap A, Cohen J, et al.
JAMA Netw Open
. 2024 Feb;
7(2):e240146.
PMID: 38386321
Importance: National implementation of rapid trio genome sequencing (rtGS) in a clinical acute setting is essential to ensure advanced and equitable care for ill neonates. Objective: To evaluate the feasibility,...
7.
Tarabeih N, Kalinkovich A, Ashkenazi S, Cherny S, Shalata A, Livshits G
Int J Mol Sci
. 2024 Jan;
25(2).
PMID: 38255954
Metabolic syndrome (MetS) is a complex disease involving multiple physiological, biochemical, and metabolic abnormalities. The search for reliable biomarkers may help to better elucidate its pathogenesis and develop new preventive...
8.
Kaiyrzhanov R, Rad A, Lin S, Bertoli-Avella A, Kallemeijn W, Godwin A, et al.
Brain
. 2023 Nov;
147(4):1436-1456.
PMID: 37951597
The acyl-CoA-binding domain-containing protein 6 (ACBD6) is ubiquitously expressed, plays a role in the acylation of lipids and proteins and regulates the N-myristoylation of proteins via N-myristoyltransferase enzymes (NMTs). However,...
9.
Tarabeih N, Shalata A, Kalinkovich A, Higla O, Livshits G
Arch Osteoporos
. 2023 Nov;
18(1):132.
PMID: 37947892
Purpose: The reported capacity of IL-34 to induce and enhance osteoclastogenesis suggests its potential involvement in the pathogenesis of osteoporosis. Our study aimed to evaluate whether there is an association...
10.
Tarabeih N, Kalinkovich A, Shalata A, Higla O, Livshits G
Biomolecules
. 2023 Sep;
13(9).
PMID: 37759715
Knee osteoarthritis (KOA) is one of the most common progressive, age-dependent chronic degenerative joint diseases. KOA often develops as a result of a gradual articular cartilage loss caused by its...