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Publications by Megan Piazza
A Case Report of Genetic Prion Disease With Two Different PRNP Variants
Molecular genetics & genomic medicine
Genetics
Molecular Biology
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Analysis of the Genetic Variants Associated With Recurrent Thromboembolism in a Patient With Hemoglobin H Disease Following Splenectomy: A Case Report
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Β-Amyloid 42; Prion Protein (PRNP; PrP; CD230)
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Wolfram Syndrome: Case Report of Two Siblings With Genetic Analysis
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Evaluation of 22 Genetic Variants With Crohn's Disease Risk in the Ashkenazi Jewish Population: A Case-Control Study
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Case Report: The First Probable Hong Kong Chinese Case of LPIN1-related Acute Recurrent Rhabdomyolysis in a Boy With Two Novel Variants
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