Hemidiaphragm atrophy in muscle-specific kinase myasthenia gravis von Cartwright, Michael S., Keskinyan, Vahakn S.

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A randomized, controlled trial of magnetic therapy for carpal tunnel syndrome von Baute, Vanessa, Keskinyan, Vahakn S., Sweeney, Erica R., Bowden, Kayla D., Gordon, Allison, Hutchens, Janet, Cartwright, Michael S.

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Case Report: Unusual Aggregation of Different Glomerulopathies in a Family Resolved by Genetic Testing and Reverse Phenotyping von Kumar, Reeti, Keskinyan, Vahakn, Stangl, Megan Chryst, Lane, Brandon M, Buckley, Anne F, Barisoni, Laura, Howell, David N, Gbadegesin, Rasheed A

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Feasibility and Impact of a Student-Led, Semi-Structured, Near-Peer Student Guides Program on Navigating Through Medical School von Laurence, Colleen E., Jones, Jessie R., Stone, Shane N., Moses-Hampton, Malcolm, Yates, Samuel J., Khalil, Mario E., Callese, Tyler E., Kaye, Shaina P., Wirth, Scott H., Keskinyan, Vahakn S., Bentley, Paige G., Reynolds, Patrick S., Strowd, Roy E.

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Unusual Aggregation of Different Glomerulopathies in a Family Resolved by Genetic Testing: PO1867 von Keskinyan, Vahakn S., Kumar, Reeti, Gbadegesin, Rasheed A.

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Hemidiaphragm atrophy in muscle-specific kinase myasthenia gravis: Diaphragm Atrophy in MuSK MG von Cartwright, Michael S., Keskinyan, Vahakn S.

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Evaluation of a Quality Improvement Intervention to Improve Pediatric Palliative Care Consultation Processes von Stoyell, Jennifer Forsman, Jordan, Megan, Derouin, Anne, Thompson, Julie, Gall, Sarah, Jooste, Karen R., Keskinyan, Vahakn Shant, Lakis, Kristen Register, Lee, Yu-Lin Amy, Docherty, Sharron

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FDG-PET Adapted Sequential Therapy With Brentuximab Vedotin and Augmented ICE Followed By Autologous Stem Cell Transplant For Relapsed and Refractory Hodgkin Lymphoma von Moskowitz, Alison, Schoder, Heiko, Gerecitano, John F., Hamlin, Paul, Horwitz, Steven M., Matasar, Matthew J, Keskinyan, Vahakn S, McCall, Susan, Noy, Ariela, Palomba, M. Lia, Portlock, Carol S., Straus, David J, Yahalom, Joachim, Younes, Anas, Zelenetz, Andrew D, Moskowitz, Craig H.

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Case Report: Unusual Aggregation of Different Glomerulopathies in a Family Resolved by Genetic Testing and Reverse Phenotyping von Kumar, Reeti, Keskinyan, Vahakn, Stangl, Megan Chryst, Lane, Brandon M, Buckley, Anne F, Barisoni, Laura, Howell, David N, Gbadegesin, Rasheed A

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