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검색어 : 통합검색[Developmental disabilities --Genetic aspects]

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  • 11
    Autism spectrum disorder causes, mechanisms, and treatments: focus on neuronal synapses
    Won, Hyejung; Mah, Won; Kim, Eunjoon; Department of Biological Sciences, Korea Advanced Institute of Science and Technology Daejeon, South Korea; Department of Biological Sciences, Korea Advanced Institute of Science and Technology Daejeon, South Korea; Department of Biological Sciences, Korea Advanced Institute of Science and Technology Daejeon, South Korea; (Frontiers in molecular neuroscience, v.6, 2013, pp.19)
  • 12
    <i>Dyrk1a</i> from Gene Function in Development and Physiology to Dosage Correction across Life Span in Down Syndrome
    Atas-Ozcan, Helin; Brault, Vé ronique; Duchon, Arnaud; Herault, Yann; Université de Strasbourg, CNRS, INSERM, Institut de Gé né tique et de Biologie Molé culaire et Cellulaire (IGBMC), 1 rue Laurent Fries, 67404 Illkirch Graffenstaden, France; atash@igbmc.fr (H.A.-O.); vbrault@igbmc.fr (V.B.); duchon@igbmc.fr (A.D.); Université de Strasbourg, CNRS, INSERM, Institut de Gé né tique et de Biologie Molé culaire et Cellulaire (IGBMC), 1 rue Laurent Fries, 67404 Illkirch Graffenstaden, France; atash@igbmc.fr (H.A.-O.); vbrault@igbmc.fr (V.B.); duchon@igbmc.fr (A.D.); Université de Strasbourg, CNRS, INSERM, Institut de Gé né tique et de Biologie Molé culaire et Cellulaire (IGBMC), 1 rue Laurent Fries, 67404 Illkirch Graffenstaden, France; atash@igbmc.fr (H.A.-O.); vbrault@igbmc.fr (V.B.); duchon@igbmc.fr (A.D.); Université de Strasbourg; (Genes, v.12, 2021, pp.1833)
  • 13
    A - 111 Neuropsychological Performance in CDK-13 Related Disorder: a Multi-Year Case Study
    Robinson, Mary L; Bean, Akanksha M; Krapf, Erica M; ; (Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists, v.38, 2023, pp.1283-1283)
  • 14
    Neurological Aspects of Human Glycosylation Disorders
    Freeze, Hudson H.; Eklund, Erik A.; Ng, Bobby G.; Patterson, Marc C.; Sanford-Burnham Medical Research Institute, La Jolla, California 92037; Section of Experimental Paediatrics, Department of Clinical Sciences, Lund University, SE-221 84 Lund, Sweden; Sanford-Burnham Medical Research Institute, La Jolla, California 92037; Division of Child and Adolescent Neurology, Mayo Clinic, Rochester, Minnesota 55905; (Annual review of neuroscience, v.38, 2015, pp.105-125)
  • 15
    Wolf-Hirschhorn (4p-) syndrome.
    Battaglia, A; Carey, J C; Wright, T J; ; (Advances in pediatrics, v.48, 2001, pp.75-113)
  • 16
    Developmental Ethanol Exposure Causes Reduced Feeding and Reveals a Critical Role for Neuropeptide F in Survival
    Guevara, Amanda; Gates, Hillary; Urbina, Brianna; French, Rachael; ; (Frontiers in physiology, v.9, 2018, pp.237)
  • 17
    Tourette Syndrome and Learning Disabilities
    Burd, Larry; Kauffman, David W.; Kerbeshian, Jacob; Larry Burd is an associate professor at the Departments of Neuroscience and Pediatrics at the University of North Dakota and an education specialist in the Child Evaluation and Treatment Program. He obtained his MS in special education at Eastern Montana College. His research interests include developmental disabilities, time estimation, Tourette Syndrome, and autism.; David W. Kauffman is in the doctoral program at the Department of Clinical Psychology at the Unï versity of North Dakota. His research interests include reading across the life span and developmental disorders in children.; Jacob Kerbeshian, MD, is an associate professor of neuroscience at the University of North Dakota School of Medicine. He received his MD at the University of Rochester. His research interests are developmental disorders in children, adolescents, and adults; Tourette Syndrome; and psychiatric aspects of genetic disorders. Address: Larry Burd, MCRH, 1300 So. Columbia Road, University of North Dako; (Journal of learning disabilities : LDX, v.25, 1992, pp.598-604)
  • 18
    Nondisjunction and transmission ratio distortion ofChromosome 2 in a (2.8) Robertsonian translocation mouse strain
    Schulz, Reiner; Underkoffler, Lara A.; Collins, Joelle N.; Oakey, Rebecca J.; Department of Medical and Molecular Genetics, King’s College London, 8th Floor Guy’s Tower, London, SE1 9RT United Kingdom; Division of Human Genetics, The Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania 19104 USA; Division of Human Genetics, The Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania 19104 USA; Department of Medical and Molecular Genetics, King’s College London, 8th Floor Guy’s Tower, London, SE1 9RT United Kingdom; (Mammalian genome : official journal of the International Mammalian Genome Society, v.17, 2006, pp.239-247)
  • 19
    Evidence and Open Questions for the Use of Video-Feedback Interventions With Parents of Children With Neurodevelopmental Disabilities
    Provenzi, Livio; Giusti, Lorenzo; Caglia, Marzia; Rosa, Elisa; Mascheroni, Eleonora; Montirosso, Rosario; ; (Frontiers in psychology, v.11, 2020, pp.1374)
  • 20
    Williams Syndrome: Daily Challenges and Positive Impact on the Family
    Scallan, Susan; Senior, Joyce; Reilly, Colin; National Educational Psychological Service (NEPS), Western Region, Castlebar, Mayo, Ireland; School of Education, University College Dublin, Belfield, Dublin, Ireland; School of Education, University College Dublin, Belfield, Dublin, Ireland; (Journal of applied research in intellectual disabilities : JARID, v.24, 2011, pp.181-188)
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