Journey from cognition to brain to gene :: perspectives from Williams syndrome /
A blueprint for the investigation of neurodevelopmental disorders, this book presents the work of a team of scientists using a multidisciplinary, integrated approach to link genes with human behavior. Using Williams syndrome as a model, leading researchers in neuroanatomy, neurocognition, neurophysi...
Gespeichert in:
Weitere Verfasser: | , |
---|---|
Format: | Elektronisch E-Book |
Sprache: | English |
Veröffentlicht: |
Cambridge, Mass. :
MIT Press,
©2001.
©2001 |
Schlagworte: | |
Online-Zugang: | Volltext |
Zusammenfassung: | A blueprint for the investigation of neurodevelopmental disorders, this book presents the work of a team of scientists using a multidisciplinary, integrated approach to link genes with human behavior. Using Williams syndrome as a model, leading researchers in neuroanatomy, neurocognition, neurophysiology, and molecular genetics have built bridges between disciplines to link higher cognitive functions, their underlying neurobiological bases, and their molecular genetic underpinnings. One of the book's many strengths is that the scientists from each discipline studied the same individuals with Williams syndrome. As the book shows, Williams syndrome is a fascinating disorder because of the "peaks and valleys" among cognitive domains: severe intellectual deficits but remarkably spared and effusive language; specific impairment in spatial construction but great strength in face processing and sociability. By capitalizing on these dissociations in higher cognitive functioning, the book provides a model for the study of brain-behavior relationships as well as for the mapping of brain and behavior phenotypes to the genome and beyond. Contributors Ralph Adolphs, Twyla Alvarez, Lawrence Appelbaum, Ursula Bellugi, Dennis Burian, Xiao-Ning Chen, Michael Chiles, Stephan Eliez, Albert Galaburda, Hanao Hirota, Wendy Jones, Julie Korenberg, Zona Lai, Liz Lichtenberger, Alan Lincoln, Rumiko Matsuoka, Debra Mills, Helen Neville, Judy Reilly, Allan Reiss, Bruce Roe, Marie St. George, J. Eric Schmidtt, Erica Straus |
Beschreibung: | 1 online resource (xx, 189 pages :) |
Bibliographie: | Includes bibliographical references and index. |
ISBN: | 9780262287395 0262287390 0262523124 9780262523127 1423726081 9781423726081 |
Internformat
MARC
LEADER | 00000cam a2200000 a 4500 | ||
---|---|---|---|
001 | ZDB-4-EBA-ocm61658083 | ||
003 | OCoLC | ||
005 | 20240705115654.0 | ||
006 | m o d | ||
007 | cr gn|---uuaua | ||
008 | 050623s2001 maua ob 001 0 eng d | ||
010 | |z 00054892 | ||
040 | |a YUS |b eng |e pn |c YUS |d OCLCG |d MYG |d N$T |d ZCU |d OCLCQ |d MYG |d OCLCQ |d NLGGC |d COO |d OCLCQ |d YDXCP |d OCLCQ |d CUS |d OCLCQ |d AGLDB |d OCLCO |d TOA |d OCLCO |d OCLCO |d OCLCQ |d LIP |d MERER |d OCLCQ |d OCLCO |d RRP |d OCLCA |d OCLCF |d VNS |d OCLCO |d VTS |d OCLCO |d CEF |d OCLCA |d OCLCQ |d EBLCP |d OCLCO |d REC |d MITPR |d YOU |d UUM |d STF |d M8D |d OCLCO |d OCLCQ |d OCLCA |d OCLCQ |d OCLCA |d UKAHL |d VT2 |d OCLCO |d OCLCA |d OCLCO |d OCLCQ |d COA |d OCLCO |d OCLCL | ||
019 | |a 60819841 |a 61808834 |a 251910188 |a 508263304 |a 733807844 |a 990401238 |a 990522189 |a 1167675649 |a 1286903238 |a 1340089533 | ||
020 | |a 9780262287395 |q (electronic bk.) | ||
020 | |a 0262287390 |q (electronic bk.) | ||
020 | |a 0262523124 | ||
020 | |a 9780262523127 | ||
020 | |a 1423726081 | ||
020 | |a 9781423726081 | ||
024 | 8 | |a (WaSeSS)ssj0000186240 | |
035 | |a (OCoLC)61658083 |z (OCoLC)60819841 |z (OCoLC)61808834 |z (OCoLC)251910188 |z (OCoLC)508263304 |z (OCoLC)733807844 |z (OCoLC)990401238 |z (OCoLC)990522189 |z (OCoLC)1167675649 |z (OCoLC)1286903238 |z (OCoLC)1340089533 | ||
037 | |b 00015994 | ||
037 | |a 4036 |b MIT Press | ||
037 | |a 9780262287395 |b MIT Press | ||
050 | 4 | |a RJ506.W44 |b J68 2001 | |
060 | 4 | |a QS 677 |b J86 2001 | |
072 | 7 | |a MED |x 069000 |2 bisacsh | |
072 | 7 | |a HEA |x 046000 |2 bisacsh | |
082 | 7 | |a 618.92/0042 |2 21 | |
049 | |a MAIN | ||
245 | 0 | 0 | |a Journey from cognition to brain to gene : |b perspectives from Williams syndrome / |c [edited by] Ursula Bellugi and Marie St. George. |
260 | |a Cambridge, Mass. : |b MIT Press, |c ©2001. | ||
264 | 4 | |c ©2001 | |
300 | |a 1 online resource (xx, 189 pages :) | ||
336 | |a text |b txt |2 rdacontent | ||
337 | |a computer |b c |2 rdamedia | ||
338 | |a online resource |b cr |2 rdacarrier | ||
347 | |a text file |2 rdaft | ||
504 | |a Includes bibliographical references and index. | ||
505 | 0 | 0 | |g 1. |t The neurocognitive profile of Williams syndrome : a complex pattern of strengths and weaknesses / |r by Ursula Bellugi [and others] -- |g 2. |t Hypersociability : the social and affective phenotype of Williams syndrome / |r by Wendy Jones [and others] -- |g 3. |t Neurophysiological markers of face processing in Williams syndrome / |r by Debra L. Mills [and others] -- |g 4. |t Neuroanatomy of Williams syndrome : a high-resolution MRI study / |r by Allan L. Reiss [and others] -- |g 5. |t Cellular and molecular cortical neuroanatomy i Williams syndrome / |r by Albert M. Galaburda and Ursula Bellugi -- |g 6. |t Genome structure and cognitive map of Williams syndrome / |r by Julie R. Korenberg [and others]. |
588 | 0 | |a Print version record. | |
520 | 8 | |a A blueprint for the investigation of neurodevelopmental disorders, this book presents the work of a team of scientists using a multidisciplinary, integrated approach to link genes with human behavior. Using Williams syndrome as a model, leading researchers in neuroanatomy, neurocognition, neurophysiology, and molecular genetics have built bridges between disciplines to link higher cognitive functions, their underlying neurobiological bases, and their molecular genetic underpinnings. One of the book's many strengths is that the scientists from each discipline studied the same individuals with Williams syndrome. As the book shows, Williams syndrome is a fascinating disorder because of the "peaks and valleys" among cognitive domains: severe intellectual deficits but remarkably spared and effusive language; specific impairment in spatial construction but great strength in face processing and sociability. By capitalizing on these dissociations in higher cognitive functioning, the book provides a model for the study of brain-behavior relationships as well as for the mapping of brain and behavior phenotypes to the genome and beyond. Contributors Ralph Adolphs, Twyla Alvarez, Lawrence Appelbaum, Ursula Bellugi, Dennis Burian, Xiao-Ning Chen, Michael Chiles, Stephan Eliez, Albert Galaburda, Hanao Hirota, Wendy Jones, Julie Korenberg, Zona Lai, Liz Lichtenberger, Alan Lincoln, Rumiko Matsuoka, Debra Mills, Helen Neville, Judy Reilly, Allan Reiss, Bruce Roe, Marie St. George, J. Eric Schmidtt, Erica Straus | |
546 | |a English. | ||
650 | 0 | |a Williams syndrome |x Pathophysiology. | |
650 | 0 | |a Williams syndrome |x Genetic aspects. | |
650 | 0 | |a Cognition disorders in children. |0 http://id.loc.gov/authorities/subjects/sh85027747 | |
650 | 1 | 2 | |a Williams Syndrome |x genetics |
650 | 2 | 2 | |a Brain |x pathology |
650 | 2 | 2 | |a Cognition |x physiology |
650 | 2 | 2 | |a Williams Syndrome |x physiopathology |
650 | 2 | 2 | |a Williams Syndrome |x psychology |
650 | 6 | |a Syndrome de Williams et Beuren |x Physiopathologie. | |
650 | 6 | |a Syndrome de Williams et Beuren |x Aspect génétique. | |
650 | 6 | |a Troubles de la cognition chez l'enfant. | |
650 | 7 | |a MEDICAL |x Pediatrics. |2 bisacsh | |
650 | 7 | |a HEALTH & FITNESS |x Children's Health. |2 bisacsh | |
650 | 7 | |a Cognition disorders in children |2 fast | |
653 | |a NEUROSCIENCE/General | ||
700 | 1 | |a Bellugi, Ursula, |d 1931-2022. |1 https://id.oclc.org/worldcat/entity/E39PBJfrRQPvwX8fDxf7mYCRKd | |
700 | 1 | |a St. George, Marie. |0 http://id.loc.gov/authorities/names/n00124260 | |
758 | |i has work: |a Journey from cognition to brain to gene (Text) |1 https://id.oclc.org/worldcat/entity/E39PCGjRgmh3Dqrv6rfQQxHkCP |4 https://id.oclc.org/worldcat/ontology/hasWork | ||
776 | 0 | 8 | |i Print version: |t Journey from cognition to brain to gene. |d Cambridge, Mass. : MIT Press, ©2001 |z 0262523124 |w (DLC) 00054892 |w (OCoLC)45635188 |
856 | 1 | |l FWS01 |p ZDB-4-EBA |q FWS_PDA_EBA |u https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=138534 |3 Volltext | |
856 | 1 | |l CBO01 |p ZDB-4-EBA |q FWS_PDA_EBA |u https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=138534 |3 Volltext | |
936 | |a BATCHLOAD | ||
938 | |a Askews and Holts Library Services |b ASKH |n AH37586928 | ||
938 | |a ProQuest Ebook Central |b EBLB |n EBL5340091 | ||
938 | |a EBSCOhost |b EBSC |n 138534 | ||
938 | |a YBP Library Services |b YANK |n 3411393 | ||
938 | |a YBP Library Services |b YANK |n 2363615 | ||
994 | |a 92 |b GEBAY | ||
912 | |a ZDB-4-EBA |
Datensatz im Suchindex
DE-BY-FWS_katkey | ZDB-4-EBA-ocm61658083 |
---|---|
_version_ | 1813903285108604928 |
adam_text | |
any_adam_object | |
author2 | Bellugi, Ursula, 1931-2022 St. George, Marie |
author2_role | |
author2_variant | u b ub g m s gm gms |
author_GND | http://id.loc.gov/authorities/names/n00124260 |
author_additional | by Ursula Bellugi [and others] -- by Wendy Jones [and others] -- by Debra L. Mills [and others] -- by Allan L. Reiss [and others] -- by Albert M. Galaburda and Ursula Bellugi -- by Julie R. Korenberg [and others]. |
author_facet | Bellugi, Ursula, 1931-2022 St. George, Marie |
author_sort | Bellugi, Ursula, 1931-2022 |
building | Verbundindex |
bvnumber | localFWS |
callnumber-first | R - Medicine |
callnumber-label | RJ506 |
callnumber-raw | RJ506.W44 J68 2001 |
callnumber-search | RJ506.W44 J68 2001 |
callnumber-sort | RJ 3506 W44 J68 42001 |
callnumber-subject | RJ - Pediatrics |
collection | ZDB-4-EBA |
contents | The neurocognitive profile of Williams syndrome : a complex pattern of strengths and weaknesses / Hypersociability : the social and affective phenotype of Williams syndrome / Neurophysiological markers of face processing in Williams syndrome / Neuroanatomy of Williams syndrome : a high-resolution MRI study / Cellular and molecular cortical neuroanatomy i Williams syndrome / Genome structure and cognitive map of Williams syndrome / |
ctrlnum | (OCoLC)61658083 |
dewey-full | 618.92/0042 |
dewey-hundreds | 600 - Technology (Applied sciences) |
dewey-ones | 618 - Gynecology, obstetrics, pediatrics, geriatrics |
dewey-raw | 618.92/0042 |
dewey-search | 618.92/0042 |
dewey-sort | 3618.92 242 |
dewey-tens | 610 - Medicine and health |
discipline | Medizin |
format | Electronic eBook |
fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>06062cam a2200817 a 4500</leader><controlfield tag="001">ZDB-4-EBA-ocm61658083 </controlfield><controlfield tag="003">OCoLC</controlfield><controlfield tag="005">20240705115654.0</controlfield><controlfield tag="006">m o d </controlfield><controlfield tag="007">cr gn|---uuaua</controlfield><controlfield tag="008">050623s2001 maua ob 001 0 eng d</controlfield><datafield tag="010" ind1=" " ind2=" "><subfield code="z"> 00054892 </subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">YUS</subfield><subfield code="b">eng</subfield><subfield code="e">pn</subfield><subfield code="c">YUS</subfield><subfield code="d">OCLCG</subfield><subfield code="d">MYG</subfield><subfield code="d">N$T</subfield><subfield code="d">ZCU</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">MYG</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">NLGGC</subfield><subfield code="d">COO</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">YDXCP</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">CUS</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">AGLDB</subfield><subfield code="d">OCLCO</subfield><subfield code="d">TOA</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">LIP</subfield><subfield code="d">MERER</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">OCLCO</subfield><subfield code="d">RRP</subfield><subfield code="d">OCLCA</subfield><subfield code="d">OCLCF</subfield><subfield code="d">VNS</subfield><subfield code="d">OCLCO</subfield><subfield code="d">VTS</subfield><subfield code="d">OCLCO</subfield><subfield code="d">CEF</subfield><subfield code="d">OCLCA</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">EBLCP</subfield><subfield code="d">OCLCO</subfield><subfield code="d">REC</subfield><subfield code="d">MITPR</subfield><subfield code="d">YOU</subfield><subfield code="d">UUM</subfield><subfield code="d">STF</subfield><subfield code="d">M8D</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">OCLCA</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">OCLCA</subfield><subfield code="d">UKAHL</subfield><subfield code="d">VT2</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCA</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">COA</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCL</subfield></datafield><datafield tag="019" ind1=" " ind2=" "><subfield code="a">60819841</subfield><subfield code="a">61808834</subfield><subfield code="a">251910188</subfield><subfield code="a">508263304</subfield><subfield code="a">733807844</subfield><subfield code="a">990401238</subfield><subfield code="a">990522189</subfield><subfield code="a">1167675649</subfield><subfield code="a">1286903238</subfield><subfield code="a">1340089533</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9780262287395</subfield><subfield code="q">(electronic bk.)</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">0262287390</subfield><subfield code="q">(electronic bk.)</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">0262523124</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9780262523127</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">1423726081</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9781423726081</subfield></datafield><datafield tag="024" ind1="8" ind2=" "><subfield code="a">(WaSeSS)ssj0000186240</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)61658083</subfield><subfield code="z">(OCoLC)60819841</subfield><subfield code="z">(OCoLC)61808834</subfield><subfield code="z">(OCoLC)251910188</subfield><subfield code="z">(OCoLC)508263304</subfield><subfield code="z">(OCoLC)733807844</subfield><subfield code="z">(OCoLC)990401238</subfield><subfield code="z">(OCoLC)990522189</subfield><subfield code="z">(OCoLC)1167675649</subfield><subfield code="z">(OCoLC)1286903238</subfield><subfield code="z">(OCoLC)1340089533</subfield></datafield><datafield tag="037" ind1=" " ind2=" "><subfield code="b">00015994</subfield></datafield><datafield tag="037" ind1=" " ind2=" "><subfield code="a">4036</subfield><subfield code="b">MIT Press</subfield></datafield><datafield tag="037" ind1=" " ind2=" "><subfield code="a">9780262287395</subfield><subfield code="b">MIT Press</subfield></datafield><datafield tag="050" ind1=" " ind2="4"><subfield code="a">RJ506.W44</subfield><subfield code="b">J68 2001</subfield></datafield><datafield tag="060" ind1=" " ind2="4"><subfield code="a">QS 677</subfield><subfield code="b">J86 2001</subfield></datafield><datafield tag="072" ind1=" " ind2="7"><subfield code="a">MED</subfield><subfield code="x">069000</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="072" ind1=" " ind2="7"><subfield code="a">HEA</subfield><subfield code="x">046000</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="082" ind1="7" ind2=" "><subfield code="a">618.92/0042</subfield><subfield code="2">21</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">MAIN</subfield></datafield><datafield tag="245" ind1="0" ind2="0"><subfield code="a">Journey from cognition to brain to gene :</subfield><subfield code="b">perspectives from Williams syndrome /</subfield><subfield code="c">[edited by] Ursula Bellugi and Marie St. George.</subfield></datafield><datafield tag="260" ind1=" " ind2=" "><subfield code="a">Cambridge, Mass. :</subfield><subfield code="b">MIT Press,</subfield><subfield code="c">©2001.</subfield></datafield><datafield tag="264" ind1=" " ind2="4"><subfield code="c">©2001</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 online resource (xx, 189 pages :)</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">computer</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">online resource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="347" ind1=" " ind2=" "><subfield code="a">text file</subfield><subfield code="2">rdaft</subfield></datafield><datafield tag="504" ind1=" " ind2=" "><subfield code="a">Includes bibliographical references and index.</subfield></datafield><datafield tag="505" ind1="0" ind2="0"><subfield code="g">1.</subfield><subfield code="t">The neurocognitive profile of Williams syndrome : a complex pattern of strengths and weaknesses /</subfield><subfield code="r">by Ursula Bellugi [and others] --</subfield><subfield code="g">2.</subfield><subfield code="t">Hypersociability : the social and affective phenotype of Williams syndrome /</subfield><subfield code="r">by Wendy Jones [and others] --</subfield><subfield code="g">3.</subfield><subfield code="t">Neurophysiological markers of face processing in Williams syndrome /</subfield><subfield code="r">by Debra L. Mills [and others] --</subfield><subfield code="g">4.</subfield><subfield code="t">Neuroanatomy of Williams syndrome : a high-resolution MRI study /</subfield><subfield code="r">by Allan L. Reiss [and others] --</subfield><subfield code="g">5.</subfield><subfield code="t">Cellular and molecular cortical neuroanatomy i Williams syndrome /</subfield><subfield code="r">by Albert M. Galaburda and Ursula Bellugi --</subfield><subfield code="g">6.</subfield><subfield code="t">Genome structure and cognitive map of Williams syndrome /</subfield><subfield code="r">by Julie R. Korenberg [and others].</subfield></datafield><datafield tag="588" ind1="0" ind2=" "><subfield code="a">Print version record.</subfield></datafield><datafield tag="520" ind1="8" ind2=" "><subfield code="a">A blueprint for the investigation of neurodevelopmental disorders, this book presents the work of a team of scientists using a multidisciplinary, integrated approach to link genes with human behavior. Using Williams syndrome as a model, leading researchers in neuroanatomy, neurocognition, neurophysiology, and molecular genetics have built bridges between disciplines to link higher cognitive functions, their underlying neurobiological bases, and their molecular genetic underpinnings. One of the book's many strengths is that the scientists from each discipline studied the same individuals with Williams syndrome. As the book shows, Williams syndrome is a fascinating disorder because of the "peaks and valleys" among cognitive domains: severe intellectual deficits but remarkably spared and effusive language; specific impairment in spatial construction but great strength in face processing and sociability. By capitalizing on these dissociations in higher cognitive functioning, the book provides a model for the study of brain-behavior relationships as well as for the mapping of brain and behavior phenotypes to the genome and beyond. Contributors Ralph Adolphs, Twyla Alvarez, Lawrence Appelbaum, Ursula Bellugi, Dennis Burian, Xiao-Ning Chen, Michael Chiles, Stephan Eliez, Albert Galaburda, Hanao Hirota, Wendy Jones, Julie Korenberg, Zona Lai, Liz Lichtenberger, Alan Lincoln, Rumiko Matsuoka, Debra Mills, Helen Neville, Judy Reilly, Allan Reiss, Bruce Roe, Marie St. George, J. Eric Schmidtt, Erica Straus</subfield></datafield><datafield tag="546" ind1=" " ind2=" "><subfield code="a">English.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Williams syndrome</subfield><subfield code="x">Pathophysiology.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Williams syndrome</subfield><subfield code="x">Genetic aspects.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Cognition disorders in children.</subfield><subfield code="0">http://id.loc.gov/authorities/subjects/sh85027747</subfield></datafield><datafield tag="650" ind1="1" ind2="2"><subfield code="a">Williams Syndrome</subfield><subfield code="x">genetics</subfield></datafield><datafield tag="650" ind1="2" ind2="2"><subfield code="a">Brain</subfield><subfield code="x">pathology</subfield></datafield><datafield tag="650" ind1="2" ind2="2"><subfield code="a">Cognition</subfield><subfield code="x">physiology</subfield></datafield><datafield tag="650" ind1="2" ind2="2"><subfield code="a">Williams Syndrome</subfield><subfield code="x">physiopathology</subfield></datafield><datafield tag="650" ind1="2" ind2="2"><subfield code="a">Williams Syndrome</subfield><subfield code="x">psychology</subfield></datafield><datafield tag="650" ind1=" " ind2="6"><subfield code="a">Syndrome de Williams et Beuren</subfield><subfield code="x">Physiopathologie.</subfield></datafield><datafield tag="650" ind1=" " ind2="6"><subfield code="a">Syndrome de Williams et Beuren</subfield><subfield code="x">Aspect génétique.</subfield></datafield><datafield tag="650" ind1=" " ind2="6"><subfield code="a">Troubles de la cognition chez l'enfant.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">MEDICAL</subfield><subfield code="x">Pediatrics.</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">HEALTH & FITNESS</subfield><subfield code="x">Children's Health.</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Cognition disorders in children</subfield><subfield code="2">fast</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">NEUROSCIENCE/General</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Bellugi, Ursula,</subfield><subfield code="d">1931-2022.</subfield><subfield code="1">https://id.oclc.org/worldcat/entity/E39PBJfrRQPvwX8fDxf7mYCRKd</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">St. George, Marie.</subfield><subfield code="0">http://id.loc.gov/authorities/names/n00124260</subfield></datafield><datafield tag="758" ind1=" " ind2=" "><subfield code="i">has work:</subfield><subfield code="a">Journey from cognition to brain to gene (Text)</subfield><subfield code="1">https://id.oclc.org/worldcat/entity/E39PCGjRgmh3Dqrv6rfQQxHkCP</subfield><subfield code="4">https://id.oclc.org/worldcat/ontology/hasWork</subfield></datafield><datafield tag="776" ind1="0" ind2="8"><subfield code="i">Print version:</subfield><subfield code="t">Journey from cognition to brain to gene.</subfield><subfield code="d">Cambridge, Mass. : MIT Press, ©2001</subfield><subfield code="z">0262523124</subfield><subfield code="w">(DLC) 00054892</subfield><subfield code="w">(OCoLC)45635188</subfield></datafield><datafield tag="856" ind1="1" ind2=" "><subfield code="l">FWS01</subfield><subfield code="p">ZDB-4-EBA</subfield><subfield code="q">FWS_PDA_EBA</subfield><subfield code="u">https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=138534</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="856" ind1="1" ind2=" "><subfield code="l">CBO01</subfield><subfield code="p">ZDB-4-EBA</subfield><subfield code="q">FWS_PDA_EBA</subfield><subfield code="u">https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=138534</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="936" ind1=" " ind2=" "><subfield code="a">BATCHLOAD</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">Askews and Holts Library Services</subfield><subfield code="b">ASKH</subfield><subfield code="n">AH37586928</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">ProQuest Ebook Central</subfield><subfield code="b">EBLB</subfield><subfield code="n">EBL5340091</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">EBSCOhost</subfield><subfield code="b">EBSC</subfield><subfield code="n">138534</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">YBP Library Services</subfield><subfield code="b">YANK</subfield><subfield code="n">3411393</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">YBP Library Services</subfield><subfield code="b">YANK</subfield><subfield code="n">2363615</subfield></datafield><datafield tag="994" ind1=" " ind2=" "><subfield code="a">92</subfield><subfield code="b">GEBAY</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-4-EBA</subfield></datafield></record></collection> |
id | ZDB-4-EBA-ocm61658083 |
illustrated | Illustrated |
indexdate | 2024-10-25T16:16:15Z |
institution | BVB |
isbn | 9780262287395 0262287390 0262523124 9780262523127 1423726081 9781423726081 |
language | English |
oclc_num | 61658083 |
open_access_boolean | |
owner | MAIN |
owner_facet | MAIN |
physical | 1 online resource (xx, 189 pages :) |
psigel | ZDB-4-EBA |
publishDate | 2001 |
publishDateSearch | 2001 |
publishDateSort | 2001 |
publisher | MIT Press, |
record_format | marc |
spelling | Journey from cognition to brain to gene : perspectives from Williams syndrome / [edited by] Ursula Bellugi and Marie St. George. Cambridge, Mass. : MIT Press, ©2001. ©2001 1 online resource (xx, 189 pages :) text txt rdacontent computer c rdamedia online resource cr rdacarrier text file rdaft Includes bibliographical references and index. 1. The neurocognitive profile of Williams syndrome : a complex pattern of strengths and weaknesses / by Ursula Bellugi [and others] -- 2. Hypersociability : the social and affective phenotype of Williams syndrome / by Wendy Jones [and others] -- 3. Neurophysiological markers of face processing in Williams syndrome / by Debra L. Mills [and others] -- 4. Neuroanatomy of Williams syndrome : a high-resolution MRI study / by Allan L. Reiss [and others] -- 5. Cellular and molecular cortical neuroanatomy i Williams syndrome / by Albert M. Galaburda and Ursula Bellugi -- 6. Genome structure and cognitive map of Williams syndrome / by Julie R. Korenberg [and others]. Print version record. A blueprint for the investigation of neurodevelopmental disorders, this book presents the work of a team of scientists using a multidisciplinary, integrated approach to link genes with human behavior. Using Williams syndrome as a model, leading researchers in neuroanatomy, neurocognition, neurophysiology, and molecular genetics have built bridges between disciplines to link higher cognitive functions, their underlying neurobiological bases, and their molecular genetic underpinnings. One of the book's many strengths is that the scientists from each discipline studied the same individuals with Williams syndrome. As the book shows, Williams syndrome is a fascinating disorder because of the "peaks and valleys" among cognitive domains: severe intellectual deficits but remarkably spared and effusive language; specific impairment in spatial construction but great strength in face processing and sociability. By capitalizing on these dissociations in higher cognitive functioning, the book provides a model for the study of brain-behavior relationships as well as for the mapping of brain and behavior phenotypes to the genome and beyond. Contributors Ralph Adolphs, Twyla Alvarez, Lawrence Appelbaum, Ursula Bellugi, Dennis Burian, Xiao-Ning Chen, Michael Chiles, Stephan Eliez, Albert Galaburda, Hanao Hirota, Wendy Jones, Julie Korenberg, Zona Lai, Liz Lichtenberger, Alan Lincoln, Rumiko Matsuoka, Debra Mills, Helen Neville, Judy Reilly, Allan Reiss, Bruce Roe, Marie St. George, J. Eric Schmidtt, Erica Straus English. Williams syndrome Pathophysiology. Williams syndrome Genetic aspects. Cognition disorders in children. http://id.loc.gov/authorities/subjects/sh85027747 Williams Syndrome genetics Brain pathology Cognition physiology Williams Syndrome physiopathology Williams Syndrome psychology Syndrome de Williams et Beuren Physiopathologie. Syndrome de Williams et Beuren Aspect génétique. Troubles de la cognition chez l'enfant. MEDICAL Pediatrics. bisacsh HEALTH & FITNESS Children's Health. bisacsh Cognition disorders in children fast NEUROSCIENCE/General Bellugi, Ursula, 1931-2022. https://id.oclc.org/worldcat/entity/E39PBJfrRQPvwX8fDxf7mYCRKd St. George, Marie. http://id.loc.gov/authorities/names/n00124260 has work: Journey from cognition to brain to gene (Text) https://id.oclc.org/worldcat/entity/E39PCGjRgmh3Dqrv6rfQQxHkCP https://id.oclc.org/worldcat/ontology/hasWork Print version: Journey from cognition to brain to gene. Cambridge, Mass. : MIT Press, ©2001 0262523124 (DLC) 00054892 (OCoLC)45635188 FWS01 ZDB-4-EBA FWS_PDA_EBA https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=138534 Volltext CBO01 ZDB-4-EBA FWS_PDA_EBA https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=138534 Volltext |
spellingShingle | Journey from cognition to brain to gene : perspectives from Williams syndrome / The neurocognitive profile of Williams syndrome : a complex pattern of strengths and weaknesses / Hypersociability : the social and affective phenotype of Williams syndrome / Neurophysiological markers of face processing in Williams syndrome / Neuroanatomy of Williams syndrome : a high-resolution MRI study / Cellular and molecular cortical neuroanatomy i Williams syndrome / Genome structure and cognitive map of Williams syndrome / Williams syndrome Pathophysiology. Williams syndrome Genetic aspects. Cognition disorders in children. http://id.loc.gov/authorities/subjects/sh85027747 Williams Syndrome genetics Brain pathology Cognition physiology Williams Syndrome physiopathology Williams Syndrome psychology Syndrome de Williams et Beuren Physiopathologie. Syndrome de Williams et Beuren Aspect génétique. Troubles de la cognition chez l'enfant. MEDICAL Pediatrics. bisacsh HEALTH & FITNESS Children's Health. bisacsh Cognition disorders in children fast |
subject_GND | http://id.loc.gov/authorities/subjects/sh85027747 |
title | Journey from cognition to brain to gene : perspectives from Williams syndrome / |
title_alt | The neurocognitive profile of Williams syndrome : a complex pattern of strengths and weaknesses / Hypersociability : the social and affective phenotype of Williams syndrome / Neurophysiological markers of face processing in Williams syndrome / Neuroanatomy of Williams syndrome : a high-resolution MRI study / Cellular and molecular cortical neuroanatomy i Williams syndrome / Genome structure and cognitive map of Williams syndrome / |
title_auth | Journey from cognition to brain to gene : perspectives from Williams syndrome / |
title_exact_search | Journey from cognition to brain to gene : perspectives from Williams syndrome / |
title_full | Journey from cognition to brain to gene : perspectives from Williams syndrome / [edited by] Ursula Bellugi and Marie St. George. |
title_fullStr | Journey from cognition to brain to gene : perspectives from Williams syndrome / [edited by] Ursula Bellugi and Marie St. George. |
title_full_unstemmed | Journey from cognition to brain to gene : perspectives from Williams syndrome / [edited by] Ursula Bellugi and Marie St. George. |
title_short | Journey from cognition to brain to gene : |
title_sort | journey from cognition to brain to gene perspectives from williams syndrome |
title_sub | perspectives from Williams syndrome / |
topic | Williams syndrome Pathophysiology. Williams syndrome Genetic aspects. Cognition disorders in children. http://id.loc.gov/authorities/subjects/sh85027747 Williams Syndrome genetics Brain pathology Cognition physiology Williams Syndrome physiopathology Williams Syndrome psychology Syndrome de Williams et Beuren Physiopathologie. Syndrome de Williams et Beuren Aspect génétique. Troubles de la cognition chez l'enfant. MEDICAL Pediatrics. bisacsh HEALTH & FITNESS Children's Health. bisacsh Cognition disorders in children fast |
topic_facet | Williams syndrome Pathophysiology. Williams syndrome Genetic aspects. Cognition disorders in children. Williams Syndrome genetics Brain pathology Cognition physiology Williams Syndrome physiopathology Williams Syndrome psychology Syndrome de Williams et Beuren Physiopathologie. Syndrome de Williams et Beuren Aspect génétique. Troubles de la cognition chez l'enfant. MEDICAL Pediatrics. HEALTH & FITNESS Children's Health. Cognition disorders in children |
url | https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=138534 |
work_keys_str_mv | AT bellugiursula journeyfromcognitiontobraintogeneperspectivesfromwilliamssyndrome AT stgeorgemarie journeyfromcognitiontobraintogeneperspectivesfromwilliamssyndrome |