Nephrotic Syndrome Induced by Tiopronin in a Male Patient with Cystinuria
V Karanfilovski, A Severova Stojanoska, V Ristovska, J Gjorgjievska, V Tasic, T Arsov, P Dzekova-Vidimliski, D Plaseska-Karanfilska, I Nikolov, N Gjorgjievski
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
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
G Protein-Coupled Receptor 35 Holds Potential as a Beacon of Hope for Treating Chondrosarcoma
A Tuncal, R Kalkan
Novel KIF11 Variants with New Clinical Features: Expanding the Clinical Phenotype
T Apuhan, A Saglam Kubra, M Yilmaz, O Bebek, S.A Demiroglu, O Demir, H.A Cebi, A Turkyilmaz
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
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
Strengthening of Ultra-High Performance Concrete Beams with CFRP Strips
Ali Khalid Ahmed, Mustafa Hameed Al-Allaf
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
The Expression Profile of Wnt/β-Catenin Signalling Pathway Genes in Miscarriages
E Gulseren, C B A Garber, T Hamad Al, A C Ozay, G Mocan, G S Temel, C M Ergoren
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