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
Partial Trisomy of Chromosome 9 Inherited by Adjacent Segregation 2 of a Balanced Reciprocal Translocation in the Mother: Rare Mechanism in Chromosomal Abnormalities
K Zerrouki, F E Aouni, F Smaili, J Ahmidi, S Meziane, K Ahmidouch, M Tajir
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
G Protein-Coupled Receptor 35 Holds Potential as a Beacon of Hope for Treating Chondrosarcoma
A Tuncal, R Kalkan
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
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
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
A Study on Construction Schedule Management Methods under Disruptive Conditions Based on Combinatorial Thinking
Jingyi Chen, Zhengfeng Ma, Chen Yang, Jiangyu Xiong, Haoyun Yang
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
Impact of Solid Fuel Use on Household Air Pollution and Respiratory Health in Two Low‑Income Communities in Mpumalanga, South Africa
Bianca Wernecke, Kristy Langerman, Angela Mathee, Nada Abdelatif, Marcus A. Howard, Nkosana Jafta, Christiaan Pauw, Shumani Phaswana, Kareshma Asharam, Ishen Seocharan, Hendrik Smith, Rajen N. Naidoo, Natasha Naidoo, Caradee Y. Wright
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