ELMOUHDI. A

Characterization of Autonomic Dysfunction in AL Cardiac Amyloidosis: A Moroccan Case Series Study

ELMOUHDI. A, ELMOKRI ELMGHARI. A, TABAT. M, AROUS. S, BENNOUNA. G, DRIGHIL. A & HABBAL. R · Asian Journal of Research in Cardiovascular Diseases · 2025

Cardiac amyloidosis is a rare but serious manifestation of systemic amyloidosis, presenting diagnostic and therapeutic challenges. The AL subtype is the most common, though transthyretin-related forms are increasingly recognized due to population aging. One frequent complication...

Open access Research Article 10.9734/ajrcd/2025/v7i1124

Structural and Functional Intersection: A Case of ACS with Anomalous Left Circumflex Artery

ELMOUHDI. A, ELMOKRI ELMGHARI. A, HALIM. S, AROUS. S, BENNOUNA. G, DRIGHIL. A & HABBAL. R · Asian Journal of Case Reports in Medicine and Health · 2025

Acute Coronary Syndrome (ACS) and coronary artery anomalies are both major contributors to cardiovascular morbidity and mortality. While ACS is commonly due to atherosclerotic processes, coronary artery anomalies (CAA) are relatively rare, occurring in approximately 0.6–1.3% of p...

Open access Research Article 10.9734/ajcrmh/2025/v8i1239

Mechanical Support in Critical Coronary Syndromes: Early Ventricular Assist Devices for LMCA Occlusion with Cardiogenic Shock

ELMOUHDI. A, BOUZIANE. M, BENNOUNA. G, DRIGHIL. A & HABBAL. R · Asian Journal of Cardiology Research · 2025

Acute occlusion of the Left main coronary artery (LMCA) is a rare but very serious angiographic finding with short-term life-threatening consequences. The clinical presentation is severe, with a high incidence of cardiogenic shock and sudden death. Treatment must be rapid and org...

Open access Research Article 10.9734/ajcr/2025/v8i1269