Browse Items (3 total)
Sort by:
Tags: 2004, Barch D M, Biological psychiatry, Cognition, cognitive assessment, cognitive enhancement, Cohen J, Essock S, Fenton W S, Frese F, Gold J M, Goldberg T E, Green M F, Heaton R K, impairment, Journal Article or Conference Abstract Publication, Keefe R S E, Kern R S, Kraemer H, Marder S R, Memory, neural basis, neurocognition, neurocognitive deficits, neuroleptic-naive, neuropsychological function, Neurosciences & Neurology, Nuechterlein K H, Performance, Psychiatry, Psychopharmacology, risperidone, Schizophrenia, siblings, Stover E, thought-disorder, Weinberger D R, Zalcman S
Tags: 2009, Academic Emergency Medicine, acute pain, cognitive, Department of Family & Community Medicine, department patients, elderly emergency, Emergency Medical Services, Emergency Medicine, Emergency Service, Force Saem Geriatric Task, Geriatrics, Gerson L W, Health Care, Health Services for the Aged, hip fracture patients, Hospital, Hustey F M, Hwang U, impairment, Journal Article, Miller D K, NEOMED College of Medicine, nursing-homes, of health care, of-care, older emergency, quality, Quality Indicators, Terrell K M, Transitional Care, Wenger N S
Tags: 2019, Adult, Antonellis Anthony, Baras Aris, Biochemistry & Molecular Biology, Brigatti Karlla W, Carson Vincent J, Catalytic Domain, Child, Demczko Matthew M, Female, Fox Michael D, Furuya Katryn N, gene, Genetic Diseases, Genetic Predisposition to Disease, Genetics & Heredity, Gonzaga-Jauregui Claudia, Griffin Laurie B, Hearing Loss, Heterozygote, Homozygote, Human molecular genetics, Humans, impairment, Inborn, Infant, Jinks Robert N, Kandula Vinay V R, lactic-acidosis, Loss of Function Mutation, Male, Martinez Erick D, mechanisms, Miles Lili, Mutation, myopathy, NEOMED College of Medicine Student, NEOMED Student Publications, Newborn, onset, Overton John D, Pedigree, Phenotype, phenotypic variability, Poskitt Laura, Preschool, Puffenberger Erik G, Radhakrishnan Kadakkal, recessive mutations, Reid Jeffrey G, Sensorineural, September 2019 Update, Severity of Illness Index, Strauss Kevin A, swiss-model, Tyrosine-tRNA Ligase, variant, Wenger Olivia K, Whole Exome Sequencing, Williams Katie B, Yeasts, Yoder Mark A