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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
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Increased prevalence of inattention-related symptoms in a large cohort of patients with congenital heart diseaseEuropean child & adolescent psychiatry, 2021-04, Vol.30 (4), p.647-655 [Peer Reviewed Journal]Springer-Verlag GmbH Germany, part of Springer Nature 2020 ;COPYRIGHT 2021 Springer ;Springer-Verlag GmbH Germany, part of Springer Nature 2020. ;ISSN: 1018-8827 ;EISSN: 1435-165X ;DOI: 10.1007/s00787-020-01547-y ;PMID: 32394091Full text available |
| 2 |
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Italian recommendations for diagnosis and management of congenital myasthenic syndromesNeurological sciences, 2019-03, Vol.40 (3), p.457-468 [Peer Reviewed Journal]Fondazione Società Italiana di Neurologia 2018 ;Neurological Sciences is a copyright of Springer, (2018). All Rights Reserved. ;ISSN: 1590-1874 ;EISSN: 1590-3478 ;DOI: 10.1007/s10072-018-3682-x ;PMID: 30554356Full text available |
| 3 |
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Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort studyBritish journal of psychiatry, 2020-05, Vol.216 (5), p.275-279 [Peer Reviewed Journal]Copyright © The Authors 2020 ;ISSN: 0007-1250 ;EISSN: 1472-1465 ;DOI: 10.1192/bjp.2019.262 ;PMID: 31964429Full text available |
| 4 |
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Two-sample Mendelian randomization study does not reveal a significant relationship between cytomegalovirus (CMV) infection and autism spectrum disorderBMC psychiatry, 2023-08, Vol.23 (1), p.559-559, Article 559 [Peer Reviewed Journal]2023. The Author(s). ;COPYRIGHT 2023 BioMed Central Ltd. ;2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2023 ;ISSN: 1471-244X ;EISSN: 1471-244X ;DOI: 10.1186/s12888-023-05035-w ;PMID: 37533011Full text available |
| 5 |
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Management of Sleep Disturbances Associated with Smith-Magenis SyndromeCNS drugs, 2020-07, Vol.34 (7), p.723-730 [Peer Reviewed Journal]Springer Nature Switzerland AG 2020 ;Copyright Springer Nature B.V. Jul 2020 ;ISSN: 1172-7047 ;EISSN: 1179-1934 ;DOI: 10.1007/s40263-020-00733-5Full text available |
| 6 |
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A case of schizophrenia with congenital color vision deficiency: From the perspective of color universal design to promote medication adherenceNeuropsychopharmacology reports, 2022-09, Vol.42 (3), p.384-386 [Peer Reviewed Journal]2022 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Society of Neuropsychopharmacology. ;2022. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2574-173X ;EISSN: 2574-173X ;DOI: 10.1002/npr2.12278 ;PMID: 35751444Full text available |
| 7 |
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Acetazolamide can improve symptoms and signs in ion channel-related congenital myopathyJournal of neurology, neurosurgery and psychiatry, 2019-02, Vol.90 (2), p.243-245 [Peer Reviewed Journal]Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2019. All rights reserved. No commercial use is permitted unless otherwise expressly granted. ;2019 Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2019. All rights reserved. No commercial use is permitted unless otherwise expressly granted. ;ISSN: 0022-3050 ;EISSN: 1468-330X ;DOI: 10.1136/jnnp-2017-317849 ;PMID: 29769250Full text available |
| 8 |
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Executive Function in Children and Adolescents with Critical Cyanotic Congenital Heart DiseaseJournal of the International Neuropsychological Society, 2015-01, Vol.21 (1), p.34-49 [Peer Reviewed Journal]Copyright © The International Neuropsychological Society 2014 ;ISSN: 1355-6177 ;EISSN: 1469-7661 ;DOI: 10.1017/S1355617714001027 ;PMID: 25487044Full text available |
| 9 |
Material Type: Article
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ADHD symptomatology of children with congenital heart disease 10 years after cardiac surgery: the role of age at operationBMC psychiatry, 2021-06, Vol.21 (1), p.316-316, Article 316 [Peer Reviewed Journal]COPYRIGHT 2021 BioMed Central Ltd. ;2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 1471-244X ;EISSN: 1471-244X ;DOI: 10.1186/s12888-021-03324-w ;PMID: 34167512Full text available |
| 10 |
Material Type: Article
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Dysregulation of kisspeptin and neurogenesis at adolescence link inborn immune deficits to the late onset of abnormal sensorimotor gating in congenital psychological disordersMolecular psychiatry, 2010-04, Vol.15 (4), p.415-425 [Peer Reviewed Journal]COPYRIGHT 2010 Nature Publishing Group ;Copyright Nature Publishing Group Apr 2010 ;Nature Publishing Group 2010. ;ISSN: 1359-4184 ;EISSN: 1476-5578 ;DOI: 10.1038/mp.2009.66 ;PMID: 19636313Full text available |
| 11 |
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Association of family history of schizophrenia and clinical outcomes in individuals with eating disordersPsychological medicine, 2023-01, Vol.53 (2), p.371-378 [Peer Reviewed Journal]Copyright © The Author(s), 2021. Published by Cambridge University Press ;Copyright © The Author(s), 2021. Published by Cambridge University Press. This work is licensed under the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 2021 The Author(s) ;ISSN: 0033-2917 ;ISSN: 1469-8978 ;EISSN: 1469-8978 ;DOI: 10.1017/S0033291721001574 ;PMID: 33926592Full text available |
| 12 |
Material Type: Article
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Brain volumes in adults with congenital heart disease correlate with executive function abilitiesBrain imaging and behavior, 2021-10, Vol.15 (5), p.2308-2316 [Peer Reviewed Journal]The Author(s) 2021 ;2021. The Author(s). ;The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1931-7557 ;EISSN: 1931-7565 ;DOI: 10.1007/s11682-020-00424-1 ;PMID: 33515180Full text available |
| 13 |
Material Type: Article
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Complementary mutations in seipin gene in a patient with Berardinelli–Seip congenital lipodystrophy and dystonia: phenotype variability suggests multiple roles of seipin geneJournal of neurology, neurosurgery and psychiatry, 2009-10, Vol.80 (10), p.1180-1181 [Peer Reviewed Journal]BMJ Publishing Group Ltd. All rights reserved. ;Copyright: 2009 BMJ Publishing Group Ltd. All rights reserved. ;ISSN: 0022-3050 ;EISSN: 1468-330X ;DOI: 10.1136/jnnp.2008.165977 ;PMID: 19762912 ;CODEN: JNNPAUFull text available |
| 14 |
Material Type: Article
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A 2020 centenary perspective on neuromuscular disordersJournal of neurology, neurosurgery and psychiatry, 2020-08, Vol.91 (8), p.791-792 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. ;2020 Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2020 ;ISSN: 0022-3050 ;EISSN: 1468-330X ;DOI: 10.1136/jnnp-2020-324327 ;PMID: 32665324Full text available |
| 15 |
Material Type: Article
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Clinical and genetic characterization of an Italian family with slow-channel syndromeNeurological sciences, 2019-03, Vol.40 (3), p.503-507 [Peer Reviewed Journal]Springer-Verlag Italia S.r.l., part of Springer Nature 2018 ;Neurological Sciences is a copyright of Springer, (2018). All Rights Reserved. ;ISSN: 1590-1874 ;EISSN: 1590-3478 ;DOI: 10.1007/s10072-018-3645-2 ;PMID: 30542963Full text available |
| 16 |
Material Type: Article
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Expanding the spectrum of genes responsible for hereditary motor neuropathiesJournal of neurology, neurosurgery and psychiatry, 2019-10, Vol.90 (10), p.1171-1179 [Peer Reviewed Journal]Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ. ;2019 Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0022-3050 ;EISSN: 1468-330X ;DOI: 10.1136/jnnp-2019-320717 ;PMID: 31167812Full text available |
| 17 |
Material Type: Article
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Additive effect of congenital heart disease and early developmental disorders on attention-deficit/hyperactivity disorder and autism spectrum disorder: a nationwide population-based longitudinal studyEuropean child & adolescent psychiatry, 2017-11, Vol.26 (11), p.1351-1359 [Peer Reviewed Journal]Springer-Verlag Berlin Heidelberg 2017 ;European Child & Adolescent Psychiatry is a copyright of Springer, 2017. ;ISSN: 1018-8827 ;EISSN: 1435-165X ;DOI: 10.1007/s00787-017-0989-8 ;PMID: 28417257Full text available |
| 18 |
Material Type: Article
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Advances in hyperekplexia and other startle syndromesNeurological sciences, 2021-10, Vol.42 (10), p.4095-4107 [Peer Reviewed Journal]Fondazione Società Italiana di Neurologia 2021 ;Fondazione Società Italiana di Neurologia 2021. ;ISSN: 1590-1874 ;EISSN: 1590-3478 ;DOI: 10.1007/s10072-021-05493-8Full text available |
| 19 |
Material Type: Article
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Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophreniaBritish journal of psychiatry, 2001-11, Vol.179 (5), p.397-402 [Peer Reviewed Journal]Copyright © Royal College of Psychiatrists, 2001 ;ISSN: 0007-1250 ;EISSN: 1472-1465 ;DOI: 10.1192/bjp.179.5.397 ;PMID: 11689394Full text available |
| 20 |
Material Type: Article
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A case study of the utilization of clozapine treatment for treatment‐resistant schizophrenia associated with 22q11.2 deletion syndromeNeuropsychopharmacology reports, 2023-06, Vol.43 (2), p.272-276 [Peer Reviewed Journal]2023 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Society of Neuropsychopharmacology. ;2023 The Authors. Neuropsychopharmacology Reports published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Society of Neuropsychopharmacology. ;2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2574-173X ;EISSN: 2574-173X ;DOI: 10.1002/npr2.12333 ;PMID: 36929244Full text available |
Results 1 - 20 of 41,596 for All Library Resources
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