Fifteen Years of Advancing Cardiovascular Rehabilitation in Low-Resource Settings through the International Council of Cardiovascular Prevention and Rehabilitation (ICCPR) and a Look Ahead
Abraham Samuel Babu, Sherry L. Grace, Dion Candelaria, Robyn Gallagher, Aashish Contractor, Carley O’Neill, John Buckley, Gabriela Lima de Melo Ghisi
Portopulmonary Hypertension in Compensated Cirrhosis: When Haemoptysis Tells the Story
Ruxandra Stirbu, Bogdan Moldoveanu, Elena Cristina Moldoveanu, Raul Eduard Dabija, Radu Crisan-Dabija
Business Analysis of the Reddit Platform in the Post-COVID Economy
Joško Lozić, Katerina Fotova Čiković
A Primer on Wireless Technology and IoT Basics
Mamatha Balachandra, Balachandra Muniyal
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
On the Load-Carrying Capacity Determination of Railway Box-Girder Bridges Using the Reduced Stress Method
Jaroslav Odrobiňák, Josef Vičan, Richard Hlinka, Jozef Prokop, Branislav Vavák
Combined Experimental and Simulation Study on the Post-Fire Performance of RC Columns
Cherif Guergah, Malek Hamda, Mohammed Baghdadi, Abdelaziz Benmarce
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
G Protein-Coupled Receptor 35 Holds Potential as a Beacon of Hope for Treating Chondrosarcoma
A Tuncal, R Kalkan
Investigation of the Frequency of CRP Gene Polymorphism in Rheumatoid Arthritis and Associations with CRP Level and Clinical Involvements of the Disease
S Biter, I Turk, G Varkal, S Dinkçi, E Erken
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