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1دورية أكاديمية
المؤلفون: Neul, Jeffrey L, Benke, Tim A, Marsh, Eric D, Lane, Jane B, Lieberman, David N, Skinner, Steven A, Glaze, Daniel G, Suter, Bernhard, Heydemann, Peter T, Beisang, Arthur A, Standridge, Shannon M, Ryther, Robin CC, Haas, Richard H, Edwards, Lloyd J, Ananth, Amitha, Percy, Alan K
مصطلحات موضوعية: Allied Health and Rehabilitation Science, Biomedical and Clinical Sciences, Health Sciences, Clinical Research, Rare Diseases, Rett Syndrome, Brain Disorders, Neurodegenerative, Intellectual and Developmental Disabilities (IDD), Pediatric
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/3wm6x387Test
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2تقرير
المؤلفون: Lo, Kyle, Chang, Joseph Chee, Head, Andrew, Bragg, Jonathan, Zhang, Amy X., Trier, Cassidy, Anastasiades, Chloe, August, Tal, Authur, Russell, Bragg, Danielle, Bransom, Erin, Cachola, Isabel, Candra, Stefan, Chandrasekhar, Yoganand, Chen, Yen-Sung, Cheng, Evie Yu-Yen, Chou, Yvonne, Downey, Doug, Evans, Rob, Fok, Raymond, Hu, Fangzhou, Huff, Regan, Kang, Dongyeop, Kim, Tae Soo, Kinney, Rodney, Kittur, Aniket, Kang, Hyeonsu, Klevak, Egor, Kuehl, Bailey, Langan, Michael, Latzke, Matt, Lochner, Jaron, MacMillan, Kelsey, Marsh, Eric, Murray, Tyler, Naik, Aakanksha, Nguyen, Ngoc-Uyen, Palani, Srishti, Park, Soya, Paulic, Caroline, Rachatasumrit, Napol, Rao, Smita, Sayre, Paul, Shen, Zejiang, Siangliulue, Pao, Soldaini, Luca, Tran, Huy, van Zuylen, Madeleine, Wang, Lucy Lu, Wilhelm, Christopher, Wu, Caroline, Yang, Jiangjiang, Zamarron, Angele, Hearst, Marti A., Weld, Daniel S.
مصطلحات موضوعية: Computer Science - Human-Computer Interaction, Computer Science - Artificial Intelligence, Computer Science - Computation and Language
الوصول الحر: http://arxiv.org/abs/2303.14334Test
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3دورية أكاديمية
المؤلفون: Mattison, Kari, Tossing, Gilles, Mulroe, Fred, Simmons, Callum, Butler, Kameryn, Schreiber, Alison, Alsadah, Adnan, Neilson, Derek, Naess, Karin, Wedell, Anna, Wredenberg, Anna, Sorlin, Arthur, McCann, Emma, Burghel, George, Menendez, Beatriz, Hoganson, George, Botto, Lorenzo, Filloux, Francis, Aledo-Serrano, Ángel, Gil-Nagel, Antonio, Tatton-Brown, Katrina, Verbeek, Nienke, van der Zwaag, Bert, Aleck, Kyrieckos, Fazenbaker, Andrew, Balciuniene, Jorune, Dubbs, Holly, Marsh, Eric, Garber, Kathryn, Ek, Jakob, Duno, Morten, Hoei-Hansen, Christina, Deardorff, Matthew, Raca, Gordana, Quindipan, Catherine, van Hirtum-Das, Michele, Breckpot, Jeroen, Hammer, Trine, Møller, Rikke, Whitney, Andrea, Douglas, Andrew, Kharbanda, Mira, Brunetti-Pierri, Nicola, Morleo, Manuela, Nigro, Vincenzo, May, Halie, Tao, James, Sherr, Elliot, Dobyns, William, Baines, Richard, Warwicker, Jim, Parker, J, Banka, Siddharth, Campeau, Philippe, Escayg, Andrew, Argilli, Emanuela
المصدر: Brain: a journal of neurology. 146(4)
مصطلحات موضوعية: ATP6V0C, V-ATPase, VMA3, epilepsy genetics, neurodevelopmental disorders, Humans, Vacuolar Proton-Translocating ATPases, Saccharomyces cerevisiae, Epilepsy, Adenosine Triphosphate
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/8hz365sfTest
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4دورية أكاديمية
المصدر: Advances in Engineering Education. Fall 2020 8(4).
تمت مراجعته من قبل الزملاء: Y
Page Count: 7
الواصفات: COVID-19, Pandemics, Educational Change, Engineering Education, Laboratory Training, Laboratory Experiments, Problem Solving, Critical Thinking, Data Analysis, Distance Education, Online Courses, Problem Based Learning, Undergraduate Students, Computer Assisted Instruction, Electronic Learning, Role of Education
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5دورية أكاديمية
المؤلفون: Keeley, Jessica, Benson‐Goldberg, Sofia, Saldaris, Jacinta, Lariviere, Judy, Leonard, Helen, Marsh, Eric D., Demarest, Scott T., Benke, Tim A., Jacoby, Peter, Downs, Jenny
المساهمون: International Foundation for CDKL5 Research, National Institutes of Health
المصدر: American Journal of Medical Genetics Part A ; ISSN 1552-4825 1552-4833
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6دورية أكاديمية
المؤلفون: Neul, Jeffrey L., Percy, Alan K., Benke, Timothy A., Berry-Kravis, Elizabeth M., Glaze, Daniel G., Peters, Sarika U., Marsh, Eric D., An, Di, Bishop, Kathie M., Youakim, James M.
المساهمون: ACADIA Pharmaceuticals
المصدر: Pediatric Neurology ; volume 152, page 63-72 ; ISSN 0887-8994
مصطلحات موضوعية: Neurology (clinical), Developmental Neuroscience, Neurology, Pediatrics, Perinatology and Child Health
الإتاحة: https://doi.org/10.1016/j.pediatrneurol.2023.11.005Test
https://api.elsevier.com/content/article/PII:S0887899423004058?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0887899423004058?httpAccept=text/plainTest -
7دورية أكاديمية
المؤلفون: Saldaris, Jacinta, Weisenberg, Judith, Pestana-Knight, Elia, Marsh, Eric D, Suter, Bernhard, Rajaraman, Rajsekar, Heidary, Gena, Olson, Heather E, Devinsky, Orrin, Price, Dana, Jacoby, Peter, Leonard, Helen, Benke, Tim A, Demarest, Scott, Downs, Jenny
المصدر: Journal of Child Neurology. 36(11)
مصطلحات موضوعية: Biomedical and Clinical Sciences, Neurosciences, Clinical Sciences, Brain Disorders, Clinical Research, Child, Epileptic Syndromes, Female, Humans, Interviews as Topic, Male, Neurologists, Outcome Assessment, Health Care, Patient Acuity, Psychometrics, Reproducibility of Results, Spasms, Infantile, Surveys and Questionnaires, CDKL5 deficiency disorder, clinical severity, outcome measure, think aloud, content validity, Cognitive Sciences, Neurology & Neurosurgery, Clinical sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/4fq5t8x6Test
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8دورية أكاديمية
المؤلفون: Shieh, Christine, Jones, Natasha, Vanle, Brigitte, Au, Margaret, Huang, Alden Y, Silva, Ana PG, Lee, Hane, Douine, Emilie D, Otero, Maria G, Choi, Andrew, Grand, Katheryn, Taff, Ingrid P, Delgado, Mauricio R, Hajianpour, MJ, Seeley, Andrea, Rohena, Luis, Vernon, Hilary, Gripp, Karen W, Vergano, Samantha A, Mahida, Sonal, Naidu, Sakkubai, Sousa, Ana Berta, Wain, Karen E, Challman, Thomas D, Beek, Geoffrey, Basel, Donald, Ranells, Judith, Smith, Rosemarie, Yusupov, Roman, Freckmann, Mary-Louise, Ohden, Lisa, Davis-Keppen, Laura, Chitayat, David, Dowling, James J, Finkel, Richard, Dauber, Andrew, Spillmann, Rebecca, Pena, Loren DM, Metcalfe, Kay, Splitt, Miranda, Lachlan, Katherine, McKee, Shane A, Hurst, Jane, Fitzpatrick, David R, Morton, Jenny EV, Cox, Helen, Venkateswaran, Sunita, Young, Juan I, Marsh, Eric D, Nelson, Stanley F, Martinez, Julian A, Graham, John M, Kini, Usha, Mackay, Joel P, Pierson, Tyler Mark
المصدر: Genetics in Medicine. 22(5)
مصطلحات موضوعية: Genetics, Clinical Research, Congenital Structural Anomalies, Brain Disorders, Pediatric, Intellectual and Developmental Disabilities (IDD), 2.1 Biological and endogenous factors, Aetiology, Child, Female, GATA Transcription Factors, Humans, Intellectual Disability, Megalencephaly, Neurodevelopmental Disorders, Nucleosomes, Phenotype, Pregnancy, Repressor Proteins, GATAD2B, NuRD complex, apraxia of speech, chromatin remodeling, macrocephaly, Undiagnosed Diseases Network, GATAD2B, NuRD complex, apraxia of speech, chromatin remodeling, macrocephaly, Clinical Sciences, Genetics & Heredity
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/7683d0mfTest
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9دورية أكاديمية
المؤلفون: Shieh, Christine, Jones, Natasha, Vanle, Brigitte, Au, Margaret, Huang, Alden Y, Silva, Ana PG, Lee, Hane, Douine, Emilie D, Otero, Maria G, Choi, Andrew, Grand, Katheryn, Taff, Ingrid P, Delgado, Mauricio R, Hajianpour, MJ, Seeley, Andrea, Rohena, Luis, Vernon, Hilary, Gripp, Karen W, Vergano, Samantha A, Mahida, Sonal, Naidu, Sakkubai, Sousa, Ana Berta, Wain, Karen E, Challman, Thomas D, Beek, Geoffrey, Basel, Donald, Ranells, Judith, Smith, Rosemarie, Yusupov, Roman, Freckmann, Mary-Louise, Ohden, Lisa, Davis-Keppen, Laura, Chitayat, David, Dowling, James J, Finkel, Richard, Dauber, Andrew, Spillmann, Rebecca, Pena, Loren DM, Metcalfe, Kay, Splitt, Miranda, Lachlan, Katherine, McKee, Shane A, Hurst, Jane, Fitzpatrick, David R, Morton, Jenny EV, Cox, Helen, Venkateswaran, Sunita, Young, Juan I, Marsh, Eric D, Nelson, Stanley F, Martinez, Julian A, Graham, John M, Kini, Usha, Mackay, Joel P, Pierson, Tyler Mark
المصدر: Genetics in Medicine. 22(4)
مصطلحات موضوعية: Biological Sciences, Genetics, Undiagnosed Diseases Network, Clinical Sciences, Genetics & Heredity
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/53c7t7b0Test
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10دورية أكاديميةAn mtDNA mutant mouse demonstrates that mitochondrial deficiency can result in autism endophenotypes
المؤلفون: Yardeni, Tal, Cristancho, Ana G., McCoy, Almedia J., Schaefer, Patrick M., McManus, Meagan J., Marsh, Eric D., Wallace, Douglas C.
المصدر: Proceedings of the National Academy of Sciences of the United States of America, 2021 Feb 01. 118(6), 1-11.
الوصول الحر: https://www.jstor.org/stable/27006277Test