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Publications by Mario Cinelli
Glu89Gln Transthyretin-Related Amyloidosis in Italy and Bulgaria: Does Geographic Area Influence Phenotype Beyond the Shared Mutation?
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Related publications
Cardiomyopathy Related to Transthyretin Val30met Mutation in Hereditary Systemic Amyloidosis
ARQUIVOS BRASILEIROS DE CARDIOLOGIA - IMAGEM CARDIOVASCULAR
Fibroblasts Endocytose and Degrade Transthyretin Aggregates in Transthyretin-Related Amyloidosis
Laboratory Investigation
Forensic Medicine
Pathology
Cell Biology
Molecular Biology
The V122I Mutation in Hereditary Transthyretin-Mediated Amyloidosis Is Significantly Associated With Polyneuropathy
Journal of Cardiac Failure
Cardiovascular Medicine
Cardiology
Transthyretin Cardiac Amyloidosis in Black Americans
Circulation. Heart failure
Medicine
Cardiovascular Medicine
Cardiology
Recent Advances in Transthyretin Amyloidosis Therapy
Translational Neurodegeneration
Molecular Neuroscience
Neurology
Cellular
Cognitive Neuroscience
Identifying Mixed Phenotype: Evaluating the Presence of Polyneuropathy in Patients With Hereditary Transthyretin-Mediated Amyloidosis With Cardiomyopathy
Journal of Cardiac Failure
Cardiovascular Medicine
Cardiology
Autosomal-Dominant Transthyretin (TTR)-related Amyloidosis Is Not a Frequent CMT2 Neuropathy “In Disguise”
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
An Unusual Case of Hereditary Transthyretin‐related Amyloidosis and Ulcerative Colitis in a Young Indian Girl
JGH Open
Hepatology
Gastroenterology
Non-Invasive Cardiac Imaging Methods in Transthyretin Amyloidosis
Kardiologia Polska
Cardiovascular Medicine
Cardiology
