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1Academic Journal
المؤلفون: Perdue M. V., Mascheretti S., Kornilov S. A., Jasinska K. K., Ryherd K., Einar Mencl W., Frost S. J., Grigorenko E. L., Pugh K. R., Landi N.
المساهمون: Perdue, M. V., Mascheretti, S., Kornilov, S. A., Jasinska, K. K., Ryherd, K., Einar Mencl, W., Frost, S. J., Grigorenko, E. L., Pugh, K. R., Landi, N.
مصطلحات موضوعية: Common genetic variant, FMRI, General population, SETBP1, Single nucleotide polymorphism (SNP), Targeted association, Working memory
Relation: info:eu-repo/semantics/altIdentifier/pmid/30009840; info:eu-repo/semantics/altIdentifier/wos/WOS:000493912900006; volume:130; firstpage:44; lastpage:51; numberofpages:8; journal:NEUROPSYCHOLOGIA; https://hdl.handle.net/11571/1476518; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85052146606
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2eBook
المؤلفون: Pugh, Kenneth R., author, Frost, Stephen J., author, Sandak, Rebecca, author, Landi, Nicole, author, Moore, Dina, author, Della Porta, Gina, author, Rueckl, Jay G., author, Einar Mencl, W., author
المصدر: The Neural Basis of Reading, 2010.
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3
المؤلفون: Pugh, KR, Frost, SJ, Rothman, DL, Hoeft, F, Del Tufo, SN, Mason, GF, Molfese, PJ, Einar Mencl, W, Grigorenko, EL, Landi, N, Preston, JL, Jacobsen, L, Seidenberg, MS, Fulbright, RK
المصدر: The Journal of neuroscience : the official journal of the Society for Neuroscience, vol 34, iss 11
Pugh, KR; Frost, SJ; Rothman, DL; Hoeft, F; Del Tufo, SN; Mason, GF; et al.(2014). Glutamate and choline levels predict individual differences in reading ability in emergent readers. Journal of Neuroscience, 34(11), 4082-4089. doi: 10.1523/JNEUROSCI.3907-13.2014. UCSF: Retrieved from: http://www.escholarship.org/uc/item/4mt3w49zمصطلحات موضوعية: Male, Aspartic Acid, MRS, Neurology & Neurosurgery, Magnetic Resonance Spectroscopy, decoding, reading disability, Psychology and Cognitive Sciences, Individuality, Brain, Glutamic Acid, Vocabulary, Medical and Health Sciences, Choline, Dyslexia, Predictive Value of Tests, Phonetics, reading, Humans, Learning, Female, Child, individual differences, phonological processing, gamma-Aminobutyric Acid
وصف الملف: application/pdf
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4Academic Journal
المؤلفون: Gulhan Ercan-Sencicek, A., Davis Wright, Nicole R., Frost, Stephen J., Fulbright, Robert K., Felsenfeld, Susan, Hart, Lesley, Landi, Nicole, Einar Mencl, W., Sanders, Stephan J., Pugh, Kenneth R., State, Matthew W., Grigorenko, Elena L.
المصدر: Brain and Development ; volume 34, issue 8, page 700-703 ; ISSN 0387-7604
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5Academic Journal
المؤلفون: Frost, Stephen J., Einar Mencl, W., Sandak, Rebecca, Moore, Dina L., Rueckl, Jay G., Katz, Leonard, Fulbright, Robert K., Pugh, Kenneth R.
المصدر: NeuroReport ; volume 16, issue 6, page 621-624 ; ISSN 0959-4965
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6Academic Journal
المؤلفون: Shaywitz, Bennett A., Shaywitz, Sally E., Fulbright, Robert K., Skudlarski, Pawel, Pugh, Kenneth R., Einar Mencl, W., Constable, Todd, Marchione, Karen, Holahan, John, Lee, JunRen, Jenner, Annette R., Fletcher, Jack, Lyon, Reid, Gore, John C.
المصدر: NeuroImage ; volume 13, issue 6, page 838 ; ISSN 1053-8119
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7Academic Journal
المساهمون: Gulhan Ercan-Sencicek, A (authoraut), Davis Wright, Nicole R (authoraut), Frost, Stephen J (authoraut), Fulbright, Robert K (authoraut), Felsenfeld, Susan (authoraut), Hart, Lesley (authoraut), Landi, Nicole (authoraut), Einar Mencl, W (authoraut), Sanders, Stephan J (authoraut), Pugh, Kenneth R (authoraut), State, Matthew W (authoraut), Grigorenko, Elena L (authoraut)
مصطلحات موضوعية: Abnormalities, Multiple, Autistic Disorder, Child, Chromosome Disorders, Chromosome Duplication, Chromosomes, Human, Pair 17, Humans, Language Disorders/etiology, Male, Phenotype, Smith-Magenis Syndrome/complications, Smith-Magenis Syndrome/genetics, Smith-Magenis Syndrome/physiopathology
وصف الملف: 1 online resource; computer
Relation: Brain & development--1872-7131--1872-7131; fsu:330499; (IID) FSU_pmch_22178197; (DOI) 10.1016/j.braindev.2011.11.003; (PMCID) PMC3343226; (RID) 22178197; (EID) 22178197; (PII) S0387-7604(11)00309-3; https://diginole.lib.fsu.edu/islandora/object/fsu%3A330499/datastream/TN/view/Searching%20for%20Potocki-Lupski%20syndrome%20phenotype.jpg