The Frequency of Autoimmune N-Methyl-D-Aspartate Receptor Encephalitis Surpasses That of Individual Viral Etiologies in Young Individuals Enrolled in the California Encephalitis Pr... von Gable, Mary S., Sheriff, Heather, Dalmau, Josep, Tilley, Drake H., Glaser, Carol A.

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Anti- N -Methyl- d -Aspartate Receptor Encephalitis Appearing as a New-Onset Psychosis: Disease Course in Children and Adolescents Within the California Encephalitis Project von Gable, Mary, MD, MPH, MBA, Glaser, Carol, MD, MPH, DVM

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Sustained corticosteroid- induced mania and psychosis despite cessation: A case study and brief literature review von Gable, Mary, Depry, Dwayne

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An overview of jail-based competency restoration von Kirkorsky, Scott E., Gable, Mary, Warburton, Katherine

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210 Clinical Utility of Gene Panel and Clinical Exome Testing in Cardiac Disease von Gable, Mary, Buxton, Chris, Woodward, Geoff, Wadsley, Marc, Honeychurch, Julie, Joanne, Davies, Newbury-Ecob, Ruth, Low, Karen, Donaldson, Alan, Affleck, Josphine, Whittington, Rebecca, Greenslade, Mark, Williams, Maggie

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203 ELN Gene: UKGTN Service for SVAS and Cutis Laxa. Copy Number Variants (CNVS) Are a Common Cause of Disease von Gable, Mary, Burton-Jones, Sarah, Turner, Claire, Dean, John, Constantinou, Panayiotis, Scurr, Ingrid, Low, Karen, Wakeling, Emma, Newbury-Ecob, Ruth, Williams, Maggie

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196 Paediatric Cardiomyopathy (PC); The Validation, Implementation and Utility of a 71 Gene NGS Diagnostic Panel to Detect Variants in Rare Cardiac Genes von Gable, Mary, Honeychurch, Julie, Sawyer, Hilary, Newbury-Ecob, Ruth, Steward, Colin, Robert, Leema, Bueser, Tootie, Gardiner, Carol, Bowen, Claire, Williams, Maggie

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196Paediatric Cardiomyopathy (PC); The Validation, Implementation and Utility of a 71 Gene NGS Diagnostic Panel to Detect Variants in Rare Cardiac Genes von Gable, Mary, Honeychurch, Julie, Sawyer, Hilary, Newbury-Ecob, Ruth, Steward, Colin, Robert, Leema, Bueser, Tootie, Gardiner, Carol, Bowen, Claire, Williams, Maggie

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A unique triadin exon deletion causing a null phenotype von O’Callaghan, Barry M., Hancox, Jules C., Stuart, Alan G., Armstrong, Catherine, Williams, Maggie M., Hills, Alison, Pearce, Hazel, Dent, Carolyn L., Gable, Mary, Walsh, Mark A.

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Comparative multiplex dosage analysis detects whole exon deletions at the phenylalanine hydroxylase locus von Gable, Mary, Williams, Margaret, Stephenson, Anne, Okano, Yoshiyuki, Ring, Susan, Hurtubise, Melanie, Tyfield, Linda

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A unique triadin exon deletion causing a null phenotype von O'Callaghan, Barry M, Hancox, Jules C, Stuart, Alan G, Armstrong, Catherine, Williams, Maggie M, Hills, Alison, Pearce, Hazel, Dent, Carolyn L, Gable, Mary, Walsh, Mark A

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ZCCHC8 , the nuclear exosome targeting component, is mutated in familial pulmonary fibrosis and is required for telomerase RNA maturation von Gable, Dustin L, Gaysinskaya, Valeriya, Atik, Christine C, Talbot, Jr, C Conover, Kang, Byunghak, Stanley, Susan E, Pugh, Elizabeth W, Amat-Codina, Nuria, Schenk, Kara M, Arcasoy, Murat O, Brayton, Cory, Florea, Liliana, Armanios, Mary

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Asymmetrical hemisphere activation enhances global–local processing von Gable, Philip A., Poole, Bryan D., Cook, Mary S.

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Nurses as Leaders in Disaster Preparedness and Response-A Call to Action von Veenema, Tener Goodwin, Griffin, Anne, Gable, Alicia R., MacIntyre, Linda, Simons, RADM Nadine, Couig, Mary Pat, Walsh Jr, John J., Lavin, Roberta Proffitt, Dobalian, Aram, Larson, Elaine

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Familial Clonal Hematopoiesis in a Long Telomere Syndrome von DeBoy, Emily A., Tassia, Michael G., Schratz, Kristen E., Yan, Stephanie M., Cosner, Zoe L., McNally, Emily J., Gable, Dustin L., Xiang, Zhimin, Lombard, David B., Antonarakis, Emmanuel S., Gocke, Christopher D., McCoy, Rajiv C., Armanios, Mary

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A Syndromic Intellectual Disability Disorder Caused by Variants in TELO2, a Gene Encoding a Component of the TTT Complex von You, Jing, Sobreira, Nara L., Gable, Dustin L., Jurgens, Julie, Grange, Dorothy K., Belnap, Newell, Siniard, Ashley, Szelinger, Szabolcs, Schrauwen, Isabelle, Richholt, Ryan F., Vallee, Stephanie E., Dinulos, Mary Beth P., Valle, David, Armanios, Mary, Hoover-Fong, Julie

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An integrated framework for theories of individual attitudes toward technology von Tate, Mary, Evermann, Joerg, Gable, Guy

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Call to Action: The Case for Advancing Disaster Nursing Education in the United States von Veenema, Tener Goodwin, Lavin, Roberta Proffitt, Griffin, Anne, Gable, Alicia R., Couig, Mary Pat, Dobalian, Aram

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T cell immune deficiency rather than chromosome instability predisposes patients with short telomere syndromes to squamous cancers von Schratz, Kristen E., Flasch, Diane A., Atik, Christine C., Cosner, Zoe L., Blackford, Amanda L., Yang, Wentao, Gable, Dustin L., Vellanki, Paz J., Xiang, Zhimin, Gaysinskaya, Valeriya, Vonderheide, Robert H., Rooper, Lisa M., Zhang, Jinghui, Armanios, Mary

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Germline Mutations in DNA Repair Genes in Lung Adenocarcinoma von Parry, Erin M., Gable, Dustin L., Stanley, Susan E., Khalil, Sara E., Antonescu, Valentin, Florea, Liliana, Armanios, Mary

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