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Publications by Myrto Moutafi
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
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Diagnostic, Genetic and Therapeutic Challenges in Mixed Phenotype Acute Leukemia: A Case Report
Cancer Archives
Diagnostic Challenges in Hereditary Transthyretin Amyloidosis With Polyneuropathy: Avoiding Misdiagnosis of a Treatable Hereditary Neuropathy
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Hereditary Renal Amyloidosis With a Variant Lysozyme p.Trp82Arg in a Chinese Family: Case Report and Literature Review
BMC Nephrology
Nephrology
Hereditary Amyloid Cardiomyopathy Caused by a Variant Apolipoprotein A1
American Journal of Pathology
Forensic Medicine
Pathology
Identification of a New Hereditary Amyloidosis Prealbumin Variant, Tyr-77, and Detection of the Gene by DNA Analysis.
Journal of Clinical Investigation
Medicine
Cecal Endometriosis: A Case Report and Discussion on Management Options
Nippon Daicho Komonbyo Gakkai Zasshi
First Report of Hereditary Lysozyme Amyloidosis in a South Asian Family
Case Reports in Hematology
Nasopharyngeal and Laryngeal Amyloidosis: A Case Report
Journal of Medical Updates
Oral Involvement in a Case of AA Amyloidosis: A Case Report
Journal of Medical Case Reports
Medicine
