Ruxolitinib Discontinuation Syndrome in a Patient With Myelofibrosis to Acute Myeloid Leukemia Transformation von Shakir, Aamina T, Nusrat, Sanober, Keruakous, Amany

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Wide Complex Tachycardia in a Right-Sided Heart von Shakir, Aamina, Dominic, Paari, Amorn, Allen, Kasabali, Basel

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A SHOCKING DEVELOPMENT: ACUTE CARDIOGENIC SHOCK AFTER IBUTILIDE CARDIOVERSION DUE TO BRADYCARDIA AND RV DYSFUNCTION von Shakir, Aamina, Swaminathan, Paari Dominic

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SAFETY AND EFFICACY OF PCSK9 INHIBITORS IN FAMILIAL HYPERCHOLESTEROLEMIA: A SYSTEMATIC REVIEW AND META-ANALYSIS von Shakir, Aamina, Barron, Kyle, Modi, Kalgi A.

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The enigmatic immunoglobulin G4-related disease and its varied cardiovascular manifestations von Shakir, Aamina, Wheeler, Yurong, Krishnaswamy, Guha

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Qualitative and Quantitative Effects of PCSK9 Inhibitors in familial Hypercholesterolemia: a Synthetic Review von Shakir, Aamina, Barron, Kyle, Modi, Kalgi

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PO-05-147 RIGHT ON Q: WIDE-COMPLEX TACHYCARDIA IN SETTING OF DEXTROPOSITION von Shakir, Aamina, Dominic, Paari, Amorn, Allen M., Kasabali, Basel

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ORAL ANTICOAGULANT MONOTHERAPY VS. ORAL ANTICOAGULATION WITH SINGLE ANTIPLATELET THERAPY IN PATIENTS WITH ATRIAL FIBRILLATION AND STABLE ISCHEMIC HEART DISEASE: A SYSTEMATIC REVIEW... von Shakir, Aamina, Khan, Arsalan, Clifton, Shari, Reese, Jessica, Deshmukh, Abhishek, Asad, Zain Ul Abideen

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Wide Complex Tachycardia in a Right-Sided Heart: Diagnostic and Therapeutic Challenges von Shakir, Aamina, Dominic, Paari, Amorn, Allen, Kasabali, Basel

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Inferred inheritance of MorbidMap genes without OMIM clinical synopsis von Shakir, Aamina, Ripperger, Michael, Jiang, Zhijie, Wierenga, Klaas J

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Two Roads Diverge: Treatment Choice in Coexisting Severe Aplastic Anemia and Paroxysmal Nocturnal Hemoglobinuria von Shakir, Aamina, Narula, Sunny, LaGrow, Austin, Nusrat, Sanober

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Dual therapy with oral anticoagulation and single antiplatelet agent versus monotherapy with oral anticoagulation alone in patients with atrial fibrillation and stable ischemic hea... von Shakir, Aamina, Khan, Arsalan, Agarwal, Siddharth, Clifton, Shari, Reese, Jessica, Munir, Muhammad Bilal, Nasir, Usama Bin, Khan, Safi U., Gopinathannair, Rakesh, DeSimone, Christopher V., Deshmukh, Abhishek, Jackman, Warren M., Stavrakis, Stavros, Asad, Zain Ul Abideen

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The first case of deafness‐dystonia syndrome due to compound heterozygous variants in FITM2 von Shakir, Aamina, Wadley, Alexandrea F., Purcarin, Gabriela, Wierenga, Klaas J.

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The first case of deafness‐dystonia syndrome due to compound heterozygous variants in FITM 2 von Shakir, Aamina, Wadley, Alexandrea F., Purcarin, Gabriela, Wierenga, Klaas J.

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Two Roads Diverge: Treatment Choice in Coexisting Severe Aplastic Anemia and Paroxysmal Nocturnal Hemoglobinuria von Shakir, Aamina, Narula, Sunny, LaGrow, Austin, Nusrat, Sanober

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The first case of deafness-dystonia syndrome due to compound heterozygous variants in FITM2 von Shakir, Aamina, Wadley, Alexandrea F, Purcarin, Gabriela, Wierenga, Klaas J

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