Search Results - "Essakow, Jenna"

Acknowledging and Addressing Microaggressions: A Virtual Experiential Learning Approach for Faculty by Essakow, Jenna, Edwell, April, Smith, Elisabeth, Daya, Sneha

“…Although the ACGME and other accrediting organizations are increasingly emphasizing the importance of clinical learning environments that value diversity,…”
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A case of severe acidosis in a 12-month-old: Succinyl-CoA:3-ketoacid-CoA transferase deficiency with OXCT1 gene mutations by Dhammi, Navjot, Essakow, Jenna, Gallagher, Renata, Gaw, Cynthia

“…Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency is a rare autosomal recessive disorder that results in severe ketoacidosis due to a defect in ketone…”
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Changing the conversation: impact of guidelines designed to optimize interprofessional facilitation of simulation-based team training by Ju, Mindy, Bochatay, Naike, Werne, Alexander, Essakow, Jenna, Tsang, Lisa, Nottingham, Mary, Franzon, Deborah, Lyndon, Audrey, van Schaik, Sandrijn

“…Interprofessional simulation-based team training (ISBTT) is commonly used to optimize interprofessional teamwork in healthcare. The literature documents the…”
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Motivation to Teach: An Exploration of Faculty Volunteers Participating in a DEI Curriculum by Essakow, Jenna, Tsoi, Stephanie, Van Schaik, Sandrijn

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Standardized Patients’ Perspectives on Bias in Student Encounters by Fluet, Angelina, Essakow, Jenna, Ju, Mindy

“…Purpose Standardized patient (SP) encounters are widely used in health professional education to evaluate trainees’ clinical skills. Prior literature suggests…”
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Standardized Patients’ Perspectives on Bias in Student Encounters by Fluet, Angelina, Essakow, Jenna, Ju, Mindy

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Using Simulation to Teach Learners in Health Care Behavioral Skills Related to Diversity, Equity, and Inclusion: A Scoping Review by Daya, Sneha, Illangasekare, Tushani, Tahir, Peggy, Bochatay, Naike, Essakow, Jenna, Ju, Mindy, van Schaik, Sandrijn

“…Summary Statement Bias is commonplace in the health care environment and can negatively impact patients and their health outcomes. Simulation has long been…”
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A case of severe acidosis in a 12-month-old: Succinyl-CoA:3-ketoacidCoA transferase deficiency with gene mutations by Navjot Dhammi, Jenna Essakow, Renata Gallagher, Cynthia Gaw

“…Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency is a rare autosomal recessive disorder that results in severe ketoacidosis due to a defect in ketone…”
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1412: THE EFFECT OF RUDENESS ON CHALLENGING DIAGNOSTIC ERROR: A RANDOMIZED CONTROLLED SIMULATION TRIAL by Avesar, Michael, Erez, Amir, Essakow, Jenna, Young, Caulette, Cooper, Binyamin, Klein, Margaret, Akan, Denizhan, Chang, Todd, Rake, Alyssa

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Incidence of Hemodynamic Changes Following Intravenous Acetaminophen Administration in Critically Ill Pediatric Patients by Lee, Jimin, Ng, Angelica, Schell-Chaple, Hildy, Wong, Erika, Essakow, Jenna, Gross, Kendall

“…Acetaminophen is a commonly administered analgesic and antipyretic medication that is generally well-tolerated. Recent studies in critically ill adults and…”
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Serotonin Syndrome in an Infant Associated With Linezolid and Opioid Use by Essakow, Jenna, Jin, Lulu, Marupudi, Neelima, Wattier, Rachel, McQuillen, Patrick, Franzon, Deborah

“…Most reported cases of serotonin syndrome involve either a selective serotonin reuptake inhibitor (SSRI) or monoamine oxidase inhibitors (MAOI) and at least 1…”
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PD28-03 COMPLIANCE WITH EVIDENCE BASED BONE HEALTH MANAGEMENT IN MEN ON CHRONIC ADT: OPPORTUNITIES FOR IMPROVEMENT by Gaylis, Franklin, Gaylis, Jaclyn, McGill, Kevin, Van, Sothary Julie, Prime, Hilary, Essakow, Jenna, Calabrese, Renee, Levy, Susan S, Dato, Paul

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Genetic Mutations, Birth Lengths, Weights and Head Circumferences of Children with IGF-I Receptor Defects. Comparison with other Congenital Defects in the GH/IGF-I axis by Essakow, Jenna Lee, Lauterpacht, Aharon, Lilos, Pearl, Kauli, Rivka, Laron, Zvi

“…In recent years more and more genetic defects along the GHRH-GH-IGF-I axis have been reported. Mutations of the IGF-I receptor (R) are a rare abnormality of…”
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Homozygous MED25 mutation implicated in eye–intellectual disability syndrome by Basel-Vanagaite, Lina, Smirin-Yosef, Pola, Essakow, Jenna Lee, Tzur, Shay, Lagovsky, Irina, Maya, Idit, Pasmanik-Chor, Metsada, Yeheskel, Adva, Konen, Osnat, Orenstein, Naama, Weisz Hubshman, Monika, Drasinover, Valerie, Magal, Nurit, Peretz Amit, Gaby, Zalzstein, Yael, Zeharia, Avraham, Shohat, Mordechai, Straussberg, Rachel, Monté, Didier, Salmon-Divon, Mali, Behar, Doron M.

“…Genetic syndromes involving both brain and eye abnormalities are numerous and include syndromes such as Warburg micro syndrome, Kaufman oculocerebrofacial…”
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A case of severe acidosis in a 12-month-old: Succinyl-CoA:3-ketoacid-CoA transferase deficiency with OXCT1 gene mutations by Dhammi, Navjot, Essakow, Jenna, Gallagher, Renata, Gaw, Cynthia

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