Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Georges Moulin
Hereditary Amyloid Cardiomyopathy Caused by a Variant Apolipoprotein A1
American Journal of Pathology
Forensic Medicine
Pathology
Related publications
Hereditary ATTR Amyloidosis With Cardiomyopathy Caused by the Novel Variant Transthyretin Y114S (p.Y134S)
Internal Medicine
Internal Medicine
Medicine
Amyloid Cardiomyopathy
Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia
Biochemistry
Medicine
Genetics
Molecular Biology
Estimating Population-Level Prevalence of Wild-Type and Variant Transthyretin Amyloid Cardiomyopathy
Journal of Cardiac Failure
Cardiovascular Medicine
Cardiology
A New Genetic Variant of Hereditary Apolipoprotein A-I Amyloidosis: A Case-Report Followed by Discussion of Diagnostic Challenges and Therapeutic Options
BMC Medical Genetics
Genetics
Hereditary Variant of Diabetes Mellitus Caused by a Defect of the NEUROD1 Gene (MODY6): The First Description in Russia
Problemy Endokrinologii
Endocrinology
Metabolism
Diabetes
Noonan's Cardiomyopathy: A Non-Hypertrophic Variant.
Heart
Cardiovascular Medicine
Cardiology
Apolipoprotein B Production Reduces Lipotoxic Cardiomyopathy
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
The Circularization of Amyloid Fibrils Formed by Apolipoprotein C-Ii
Biophysical Journal
Biophysics
Apolipoprotein D: A Potential Biomarker for Cerebral Amyloid Angiopathy
Neuropathology and Applied Neurobiology
Forensic Medicine
Pathology
Neurology
Histology
Physiology