The Development of a Fuzzy Logic System Using MATLAB for Early Detection of Hereditary Cancer in BRCA1/2 Negative Cases
N Senturk, GP Volkan, Babiker Ali SM, B Dogan, L Aliyeva, OS Sag, G S Temel, M Dundar, C M Ergoren
Flexural Behavior of Concrete-Filled Steel Tube CFST Members with Initial Imperfections Due to Steel Tube Notches
Haider A. A. Al-Atabi, Ahmed A. M. Al-Shaar
Using the Lean-Based Safety Leadership Framework to Improve Operational Efficiency and Reduce Occupational Risk: Evidence from a Case Study
Tiago Rodrigues, José Carlos Sá, Ana Rita Oliveira, Peter Hines, Robert Ulewicz, Andrei Bonamigo
Molecular and Immunohistochemical Biomarkers in Colorectal Carcinoma - A Single Center Study
B Krsteska, V Filipovski, K Kubelka-Sabit, Dz Jasar, N Velickova
Association of CYP2B6 and OPRM1 Genotypes with Methadone Dose Requirements and Serum Concentrations in a Vietnamese Cohorts
Quynh Giao Nguyen, Khanh Chi Tran, Thi Phuong Dung Trinh, Huy Tan Pham, Thi Ngoc Dung Dang
Forecasting Electicity in Photovoltaic Power Plants
Aleksandra Ijačić, Damir Špago, Obrad Spaić, Dragi Tiro
Effect of Ceramic Waste Valorization on the Stabilization of Tori-Dokanmey Ferralitic Soil for Road Pavement Layers in Benin
Coovi Rocambols Thède Agbelele, Valéry K. Doko, Edem Chabi, Boris Ganmavo, Mohamed Gibigaye
Sustainable Asphalt Mixtures Using Agricultural Waste Fillers: A Systematic Review of Rice Husk Ash, Bagasse Ash and Palm Shell Ash
Liftasya Pratiwi, Elsa Eka Putri, Bayu Martanto Adji, Andriani Andriani
X-Linked Adrenoleukodystrophy in a Moroccan Patient: Genetic Diagnosis Leads to Presymptomatic Testing and Family Counseling
M Mansouri, T Smol, N Louhabe, M Rama, N Rada, N Fdil, M Bouskraoui, N Aboussair
First Report of a Familiar MYCBP2 Pathogenic Variant: Expanding the Knowledge of Neurodevelopmental Disorders
I Maleva Kostovska, P Noveski, E Sukarova-Angelovska, D Plaseska-Karanfilska
G Protein-Coupled Receptor 35 Holds Potential as a Beacon of Hope for Treating Chondrosarcoma
A Tuncal, R Kalkan
Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review
H Jelti, K Khabbache, S Bouressas, F Hacht, A Oulmaati, A Lamzouri