المؤلفون: BATTAGLIA, Giuseppe, BRUNO, Valeria Maria Gloria, FRATI, Luigi, NICOLETTI, Ferdinando, SQUITIERI, Ferdinando, Milena Cannella, Barbara Riozzi, Sara Orobello, Marion L. Maat Schieman, Eleonora Aronica, Carla Letizia Busceti, Andrea Ciarmiello, Silvia Alberti, Enrico Amico, Jenny Sassone, Simonetta Sipione

المساهمون: Battaglia, Giuseppe, Milena, Cannella, Barbara, Riozzi, Sara, Orobello, Marion L., Maat Schieman, Eleonora, Aronica, Carla Letizia, Busceti, Andrea, Ciarmiello, Silvia, Alberti, Enrico, Amico, Jenny, Sassone, Simonetta, Sipione, Bruno, Valeria Maria Gloria, Frati, Luigi, Nicoletti, Ferdinando, Squitieri, Ferdinando

مصطلحات موضوعية: ransforming growth factor-beta, brain cortex, transforming growth factor-β, huntington's disease, neurodegeneration, neurodysfunction, peripheral marker, transforming growth factor-beta

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/20082658; info:eu-repo/semantics/altIdentifier/wos/WOS:000288798000010; volume:15; issue:3; firstpage:555; lastpage:571; numberofpages:17; journal:JOURNAL OF CELLULAR AND MOLECULAR MEDICINE; http://hdl.handle.net/11573/376481Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-79953298589; http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000288798000010&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396aTest; http://www.scopus.com/inward/record.url?eid=2-s2.0-79953298589&partnerID=65&md5=c888b2ee901c0023fd11e112f022eb90Test

الإتاحة: https://doi.org/10.1111/j.1582-4934.2010.01011.xTest
http://hdl.handle.net/11573/376481Test
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000288798000010&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396aTest
http://www.scopus.com/inward/record.url?eid=2-s2.0-79953298589&partnerID=65&md5=c888b2ee901c0023fd11e112f022eb90Test

المؤلفون: BLASI, PAOLA, CALDAROLA, SARA, NOVELLETTO, ANDREA, MALASPINA, PATRIZIA, Palmerio, F, Rizzo, C, Carrozzo, R, Gibson, K. M, Deodato, F, Cappa, M, Dionisi_Vici, C

المساهمون: Blasi, P, Palmerio, F, Caldarola, S, Rizzo, C, Carrozzo, R, Gibson, Km, Novelletto, A, Deodato, F, Cappa, M, Dionisi_vici, C, Malaspina, P

مصطلحات موضوعية: succinate semialdehyde dehydrogenase, brain cortex atrophy, case report, chemical analysi, clinical feature, consanguinity, disease severity, electroencephalogram, electroencephalography, enzyme deficiency, family history, female, gene location, gene mutation, genotype, human, infant, letter, molecular genetic, muscle hypotonia, phenotype, priority journal, psychomotor disorder, reverse transcription polymerase chain reaction, speech disorder, strabismu, Base Sequence, DNA, Mental Retardation, Mutation

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/16542398; info:eu-repo/semantics/altIdentifier/wos/WOS:000235840300018; volume:69; issue:3; firstpage:294; lastpage:296; journal:CLINICAL GENETICS; http://hdl.handle.net/2108/37937Test; info:eu-repo/semantics/altIdentifier/scopus/http://www.scopus.com/inward/record.url?eid=2-s2.0-33644799832&partnerID=40&md5=13ffd8e8cc20db3c46e7c47d6434d830Test

الإتاحة: https://doi.org/10.1111/j.1399-0004.2006.00579.xTest
http://hdl.handle.net/2108/37937Test

المؤلفون: Blasi, P, Palmerio, F, Caldarola, S, Rizzo, C, Carrozzo, R, Gibson, Km, Novelletto, A, Deodato, F, Cappa, M, Dionisi_vici, C, Malaspina, P

مصطلحات موضوعية: Genotype, phenotype, letter, speech disorder, reverse transcription polymerase chain reaction, consanguinity, Mental Retardation, case report, Humans, succinate semialdehyde dehydrogenase, gene mutation, human, gene location, family history, muscle hypotonia, Base Sequence, brain cortex atrophy, chemical analysis, clinical feature, disease severity, electroencephalogram, electroencephalography, enzyme deficiency, female, genotype, infant, molecular genetics, priority journal, psychomotor disorder, strabismus, DNA, Female, Infant, Mutation, Phenotype, Succinate-Semialdehyde Dehydrogenase, Settore BIO/18 - Genetica

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od______3667::326ebdb1c436e0fb34ef7fbf9e08ce5fTest
http://hdl.handle.net/2108/37937Test

المؤلفون: Ribases, M., Ramos-Quiroga, J. A., Sanchez-Mora, C., Bosch, R., Richarte, V., Palomar, G., Gastaminza, X., Biesla, A., Muenke, Maximilian, Arcos-Burgos, Mauricio, Castellanos, Francisco Xavier

المصدر: Genes, Brain and Behavior

مصطلحات موضوعية: Keywords: G protein coupled receptor, latrophilin 3, unclassified drug, adult, amygdaloid nucleus, article, attention deficit disorder, brain cortex, case control study, caudate nucleus, cerebellum, Colombia, controlled study, developmental disorder, female, gene i Adult ADHD, Attention-deficit/hyperactivity disorder, Case-control association study, LPHN3

العلاقة: http://hdl.handle.net/1885/78498Test; https://openresearch-repository.anu.edu.au/bitstream/1885/78498/7/01_Ribases_Contribution_of_LPHN3_to_the_2011.pdf.jpgTest

الإتاحة: https://doi.org/10.1111/j.1601-183X.2010.00649.xTest
http://hdl.handle.net/1885/78498Test
https://openresearch-repository.anu.edu.au/bitstream/1885/78498/7/01_Ribases_Contribution_of_LPHN3_to_the_2011.pdf.jpgTest

المصدر: Genes, Brain and Behavior

مصطلحات الفهرس: Keywords: G protein coupled receptor; latrophilin 3; unclassified drug; adult; amygdaloid nucleus; article; attention deficit disorder; brain cortex; case control study; caudate nucleus; cerebellum; Colombia; controlled study; developmental disorder; female; gene i Adult ADHD; Attention-deficit/hyperactivity disorder; Case-control association study; LPHN3, Journal article

URL: http://hdl.handle.net/1885/78498Test