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Publications by F E Dwulet
Identification of a New Hereditary Amyloidosis Prealbumin Variant, Tyr-77, and Detection of the Gene by DNA Analysis.
Journal of Clinical Investigation
Medicine
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A New Genetic Variant of Hereditary Apolipoprotein A-I Amyloidosis: A Case-Report Followed by Discussion of Diagnostic Challenges and Therapeutic Options
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Hereditary ATTR Amyloidosis With Cardiomyopathy Caused by the Novel Variant Transthyretin Y114S (p.Y134S)
Internal Medicine
Internal Medicine
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Hereditary Lysozyme Amyloidosis Variant p.Leu102Ser Associates With Unique Phenotype
Journal of the American Society of Nephrology : JASN
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Mutation in Gelsolin Gene in Finnish Hereditary Amyloidosis
Journal of Experimental Medicine
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Hereditary Renal Amyloidosis With a Variant Lysozyme p.Trp82Arg in a Chinese Family: Case Report and Literature Review
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Rapid Identification of Escherichia Coli Pathotypes by Virulence Gene Detection With DNA Microarrays
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Mild Form of Oculocutaneous Albinism Type 1: Phenotypic Analysis of Compound Heterozygous Patients With the R402Q Variant of the TYR Gene
British Journal of Ophthalmology
Molecular Neuroscience
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Hereditary Variant of Diabetes Mellitus Caused by a Defect of the NEUROD1 Gene (MODY6): The First Description in Russia
Problemy Endokrinologii
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Brain Transcriptomic Analysis of Hereditary Cerebral Hemorrhage With Amyloidosis-Dutch Type
Frontiers in Aging Neuroscience
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Cognitive Neuroscience
