skip to main content
Language:
Search Limited to: Search Limited to: Resource type Show Results with: Show Results with: Search type Index

Results 1 - 20 of 51,437  for All Library Resources

Sorted by: Sorted by: RelevanceOr hit Enter to replace sort method
Results 1 2 3 4 5 next page
Show only
Refined by: subject: Female remove
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Comprehensive evaluation of the child with intellectual disability or global developmental delays
Comprehensive evaluation of the child with intellectual disability or global developmental delays
Material Type:
Article 		Add to My Research

Comprehensive evaluation of the child with intellectual disability or global developmental delays

Pediatrics (Evanston), 2014-09, Vol.134 (3), p.e903-e918 [Peer Reviewed Journal]

Copyright © 2014 by the American Academy of Pediatrics. ;Copyright American Academy of Pediatrics Sep 2014 ;Copyright © 2014 by the American Academy of Pediatrics 2014 ;ISSN: 0031-4005 ;EISSN: 1098-4275 ;DOI: 10.1542/peds.2014-1839 ;PMID: 25157020 ;CODEN: PEDIAU

Full text available

Citations Cited by
2
Promoting Social Interactions and Job Independence for College Students with Autism or Intellectual Disability: A Pilot Study
Promoting Social Interactions and Job Independence for College Students with Autism or Intellectual Disability: A Pilot Study
Material Type:
Article 		Add to My Research

Promoting Social Interactions and Job Independence for College Students with Autism or Intellectual Disability: A Pilot Study

Journal of autism and developmental disorders, 2016-11, Vol.46 (11), p.3583-3596 [Peer Reviewed Journal]

Springer Science+Business Media New York 2016 ;COPYRIGHT 2016 Springer ;ISSN: 0162-3257 ;EISSN: 1573-3432 ;DOI: 10.1007/s10803-016-2894-2 ;PMID: 27573857 ;CODEN: JADDDQ

Full text available

Citations Cited by
3
Biallelic pathogenic variants in the lanosterol synthase gene LSS involved in the cholesterol biosynthesis cause alopecia with intellectual disability, a rare recessive neuroectodermal syndrome
Biallelic pathogenic variants in the lanosterol synthase gene LSS involved in the cholesterol biosynthesis cause alopecia with intellectual disability, a rare recessive neuroectodermal syndrome
Material Type:
Article 		Add to My Research

Biallelic pathogenic variants in the lanosterol synthase gene LSS involved in the cholesterol biosynthesis cause alopecia with intellectual disability, a rare recessive neuroectodermal syndrome

Genetics in medicine, 2019-09, Vol.21 (9), p.2025-2035 [Peer Reviewed Journal]

2019 The Author(s) ;2019© American College of Medical Genetics and Genomics 2019 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1098-3600 ;ISSN: 1530-0366 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-019-0445-x ;PMID: 30723320

Full text available

Citations Cited by
4
Family members' reports of the technology use of family members with intellectual and developmental disabilities
Family members' reports of the technology use of family members with intellectual and developmental disabilities
Material Type:
Article 		Add to My Research

Family members' reports of the technology use of family members with intellectual and developmental disabilities

Journal of intellectual disability research, 2012-04, Vol.56 (4), p.402-414 [Peer Reviewed Journal]

2011 The Authors. Journal of Intellectual Disability Research © 2011 Blackwell Publishing Ltd ;2015 INIST-CNRS ;2011 The Authors. Journal of Intellectual Disability Research © 2011 Blackwell Publishing Ltd. ;Copyright Blackwell Publishing Ltd. Apr 2012 ;ISSN: 0964-2633 ;EISSN: 1365-2788 ;DOI: 10.1111/j.1365-2788.2011.01489.x ;PMID: 21988242 ;CODEN: JIDREN

Full text available

Citations Cited by
5
De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome
De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome
Material Type:
Article 		Add to My Research

De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome

American journal of human genetics, 2016-09, Vol.99 (3), p.711-719 [Peer Reviewed Journal]

2016 American Society of Human Genetics ;Copyright © 2016 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Sep 1, 2016 ;2016 American Society of Human Genetics. 2016 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2016.06.029 ;PMID: 27545680

Full text available

Citations Cited by
6
Genomic diagnosis for children with intellectual disability and/or developmental delay
Genomic diagnosis for children with intellectual disability and/or developmental delay
Material Type:
Article 		Add to My Research

Genomic diagnosis for children with intellectual disability and/or developmental delay

Genome medicine, 2017-05, Vol.9 (1), p.43-43, Article 43 [Peer Reviewed Journal]

Copyright BioMed Central 2017 ;The Author(s). 2017 ;ISSN: 1756-994X ;EISSN: 1756-994X ;DOI: 10.1186/s13073-017-0433-1 ;PMID: 28554332

Full text available

Citations Cited by
7
Examining the social participation of children and adolescents with Intellectual Disabilities and Autism Spectrum Disorder in relation to peers
Examining the social participation of children and adolescents with Intellectual Disabilities and Autism Spectrum Disorder in relation to peers
Material Type:
Article 		Add to My Research

Examining the social participation of children and adolescents with Intellectual Disabilities and Autism Spectrum Disorder in relation to peers

Journal of intellectual disability research, 2016-05, Vol.60 (5), p.435-443 [Peer Reviewed Journal]

2016 MENCAP and International Association of the Scientific Study of Intellectual and Developmental Disabilities and John Wiley & Sons Ltd ;2016 MENCAP and International Association of the Scientific Study of Intellectual and Developmental Disabilities and John Wiley & Sons Ltd. ;ISSN: 0964-2633 ;EISSN: 1365-2788 ;DOI: 10.1111/jir.12289 ;PMID: 27120987

Full text available

Citations Cited by
8
Improving Physical Fitness of Children with Intellectual and Developmental Disabilities through an Adapted Rhythmic Gymnastics Program in China
Improving Physical Fitness of Children with Intellectual and Developmental Disabilities through an Adapted Rhythmic Gymnastics Program in China
Material Type:
Article 		Add to My Research

Improving Physical Fitness of Children with Intellectual and Developmental Disabilities through an Adapted Rhythmic Gymnastics Program in China

BioMed research international, 2020, Vol.2020, p.2345607-10 [Peer Reviewed Journal]

Copyright © 2020 Chenchen Xu et al. ;COPYRIGHT 2020 Hindawi Limited ;Copyright © 2020 Chenchen Xu et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0 ;Copyright © 2020 Chenchen Xu et al. 2020 ;ISSN: 2314-6133 ;EISSN: 2314-6141 ;DOI: 10.1155/2020/2345607 ;PMID: 32851060

Full text available

Citations Cited by
9
Automated Detection of Repetitive Motor Behaviors as an Outcome Measurement in Intellectual and Developmental Disabilities
Automated Detection of Repetitive Motor Behaviors as an Outcome Measurement in Intellectual and Developmental Disabilities
Material Type:
Article 		Add to My Research

Automated Detection of Repetitive Motor Behaviors as an Outcome Measurement in Intellectual and Developmental Disabilities

Journal of autism and developmental disorders, 2018-05, Vol.48 (5), p.1458-1466 [Peer Reviewed Journal]

Springer Science+Business Media, LLC, part of Springer Nature 2017 ;COPYRIGHT 2018 Springer ;Journal of Autism and Developmental Disorders is a copyright of Springer, (2017). All Rights Reserved. ;ISSN: 0162-3257 ;EISSN: 1573-3432 ;DOI: 10.1007/s10803-017-3408-6 ;PMID: 29164446

Full text available

Citations Cited by
10
Anxiety Disorders in Williams Syndrome Contrasted with Intellectual Disability and the General Population: A Systematic Review and Meta-Analysis
Anxiety Disorders in Williams Syndrome Contrasted with Intellectual Disability and the General Population: A Systematic Review and Meta-Analysis
Material Type:
Article 		Add to My Research

Anxiety Disorders in Williams Syndrome Contrasted with Intellectual Disability and the General Population: A Systematic Review and Meta-Analysis

Journal of autism and developmental disorders, 2017-12, Vol.47 (12), p.3765-3777 [Peer Reviewed Journal]

The Author(s) 2016 ;COPYRIGHT 2017 Springer ;Journal of Autism and Developmental Disorders is a copyright of Springer, (2016). All Rights Reserved. ;ISSN: 0162-3257 ;EISSN: 1573-3432 ;DOI: 10.1007/s10803-016-2909-z ;PMID: 27696186

Full text available

Citations Cited by
11
Antipsychotic Use With and Without Comorbid Psychiatric Diagnosis Among Adults with Intellectual and Developmental Disabilities
Antipsychotic Use With and Without Comorbid Psychiatric Diagnosis Among Adults with Intellectual and Developmental Disabilities
Material Type:
Article 		Add to My Research

Antipsychotic Use With and Without Comorbid Psychiatric Diagnosis Among Adults with Intellectual and Developmental Disabilities

Canadian journal of psychiatry, 2018-06, Vol.63 (6), p.361-369 [Peer Reviewed Journal]

The Author(s) 2017 ;The Author(s) 2017 2017 Canadian Psychiatric Association ;ISSN: 0706-7437 ;EISSN: 1497-0015 ;DOI: 10.1177/0706743717727240 ;PMID: 28830241

Full text available

Citations Cited by
12
Diagnostic methods and recommendations for the cerebral creatine deficiency syndromes
Diagnostic methods and recommendations for the cerebral creatine deficiency syndromes
Material Type:
Article 		Add to My Research

Diagnostic methods and recommendations for the cerebral creatine deficiency syndromes

Pediatric research, 2015-03, Vol.77 (3), p.398-405 [Peer Reviewed Journal]

ISSN: 0031-3998 ;EISSN: 1530-0447 ;DOI: 10.1038/pr.2014.203 ;PMID: 25521922

Full text available

Citations Cited by
13
Genetic causes of intellectual disability in a birth cohort: A population-based study
Genetic causes of intellectual disability in a birth cohort: A population-based study
Material Type:
Article 		Add to My Research

Genetic causes of intellectual disability in a birth cohort: A population-based study

American journal of medical genetics. Part A, 2015-06, Vol.167A (6), p.1204-1214 [Peer Reviewed Journal]

2015 The Authors. Published by Wiley Periodicals, Inc. ;2015 Wiley Periodicals, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.37011 ;PMID: 25728503

Full text available

Citations Cited by
14
Adapting the EQ-5D-3L for adults with mild to moderate learning disabilities
Adapting the EQ-5D-3L for adults with mild to moderate learning disabilities
Material Type:
Article 		Add to My Research

Adapting the EQ-5D-3L for adults with mild to moderate learning disabilities

Health and quality of life outcomes, 2024-04, Vol.22 (1), p.37-37 [Peer Reviewed Journal]

2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;2024. 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) 2024 ;ISSN: 1477-7525 ;EISSN: 1477-7525 ;DOI: 10.1186/s12955-024-02254-x ;PMID: 38685039

Full text available

Citations Cited by
15
A Blind Spot? Screening for Mild Intellectual Disability and Borderline Intellectual Functioning in Admitted Psychiatric Patients: Prevalence and Associations with Coercive Measures
A Blind Spot? Screening for Mild Intellectual Disability and Borderline Intellectual Functioning in Admitted Psychiatric Patients: Prevalence and Associations with Coercive Measures
Material Type:
Article 		Add to My Research

A Blind Spot? Screening for Mild Intellectual Disability and Borderline Intellectual Functioning in Admitted Psychiatric Patients: Prevalence and Associations with Coercive Measures

PloS one, 2017-02, Vol.12 (2), p.e0168847-e0168847 [Peer Reviewed Journal]

COPYRIGHT 2017 Public Library of Science ;COPYRIGHT 2017 Public Library of Science ;2017 Nieuwenhuis et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2017 Nieuwenhuis et al 2017 Nieuwenhuis et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0168847 ;PMID: 28151977

Full text available

Citations Cited by
16
Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability
Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability
Material Type:
Article 		Add to My Research

Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability

American journal of human genetics, 2017-05, Vol.100 (5), p.725-736 [Peer Reviewed Journal]

2017 The Author(s) ;Copyright © 2017 The Author(s). Published by Elsevier Inc. All rights reserved. ;2017 The Author(s) 2017 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2017.03.010 ;PMID: 28475857

Full text available

Citations Cited by
17
Predicting adult-age mental health with childhood reading and math disability: do resilience and coping styles matter?
Predicting adult-age mental health with childhood reading and math disability: do resilience and coping styles matter?
Material Type:
Article 		Add to My Research

Predicting adult-age mental health with childhood reading and math disability: do resilience and coping styles matter?

Annals of dyslexia, 2024-04, Vol.74 (1), p.97-122 [Peer Reviewed Journal]

The Author(s) 2023 ;ISSN: 0736-9387 ;EISSN: 1934-7243 ;DOI: 10.1007/s11881-023-00290-8

Digital Resources/Online E-Resources

Citations Cited by
18
Mutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features
Mutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features
Material Type:
Article 		Add to My Research

Mutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features

American journal of human genetics, 2016-10, Vol.99 (4), p.912-916 [Peer Reviewed Journal]

2016 ;Copyright © 2016. Published by Elsevier Inc. ;Copyright Cell Press Oct 6, 2016 ;2016. 2016 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2016.07.019 ;PMID: 27616480

Full text available

Citations Cited by
19
Brief Report: Sibling Feelings Toward their Brother or Sister With or Without Autism or Intellectual Disability
Brief Report: Sibling Feelings Toward their Brother or Sister With or Without Autism or Intellectual Disability
Material Type:
Article 		Add to My Research

Brief Report: Sibling Feelings Toward their Brother or Sister With or Without Autism or Intellectual Disability

Journal of autism and developmental disorders, 2019-01, Vol.49 (1), p.404-409 [Peer Reviewed Journal]

Springer Science+Business Media, LLC, part of Springer Nature 2018 ;COPYRIGHT 2019 Springer ;Journal of Autism and Developmental Disorders is a copyright of Springer, (2018). All Rights Reserved. ;ISSN: 0162-3257 ;EISSN: 1573-3432 ;DOI: 10.1007/s10803-018-3694-7 ;PMID: 30043352

Full text available

Citations Cited by
20
Familial inheritance of the 3q29 microdeletion syndrome: case report and review
Familial inheritance of the 3q29 microdeletion syndrome: case report and review
Material Type:
Article 		Add to My Research

Familial inheritance of the 3q29 microdeletion syndrome: case report and review

BMC medical genomics, 2019-03, Vol.12 (1), p.51-51, Article 51 [Peer Reviewed Journal]

COPYRIGHT 2019 BioMed Central Ltd. ;COPYRIGHT 2019 BioMed Central Ltd. ;Copyright © 2019. 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). 2019 ;ISSN: 1755-8794 ;EISSN: 1755-8794 ;DOI: 10.1186/s12920-019-0497-4 ;PMID: 30885185

Full text available

Citations Cited by

Results 1 - 20 of 51,437  for All Library Resources

Sorted by: Sorted by: RelevanceOr hit Enter to replace sort method
Results 1 2 3 4 5 next page

Personalize your results

  1. Edit

Refine Search Results

Expand My Results

  1.   

Show only

  1. Peer-reviewed Journals (48,626)

Refine My Results

Creation Date 

From To
Refine
  1. Before 1964  (44)
  2. 1964 To 1978  (2,361)
  3. 1979 To 1993  (4,856)
  4. 1994 To 2009  (17,927)
  5. After 2009  (26,274)
  6. More options open sub menu

Subject 

  1. Humans  (50,818)
  2. Male  (44,256)
  3. Science & Technology  (42,501)
  4. Life Sciences & Biomedicine  (40,874)
  5. Adult  (23,609)
  6. Middle Aged  (19,822)
  7. Child  (15,228)
  8. Disability Evaluation  (14,854)
  9. Biological And Medical Sciences  (14,798)
  10. Adolescent  (14,487)
  11. Medical Sciences  (14,178)
  12. Aged  (14,086)
  13. Social Sciences  (10,610)
  14. Child, Preschool  (10,488)
  15. Neurosciences & Neurology  (9,616)
  16. Disability  (9,448)
  17. Clinical Neurology  (8,231)
  18. Rehabilitation  (7,932)
  19. Young Adult  (6,503)
  20. More options open sub menu

Language 

  1. English  (50,751)
  2. Japanese  (5,709)
  3. Portuguese  (472)
  4. German  (299)
  5. Spanish  (273)
  6. French  (138)
  7. Norwegian  (75)
  8. Polish  (37)
  9. Italian  (36)
  10. Chinese  (36)
  11. Swedish  (23)
  12. Turkish  (14)
  13. Russian  (6)
  14. Dutch  (6)
  15. Czech  (4)
  16. Korean  (4)
  17. Serbian  (2)
  18. Icelandic  (2)
  19. Afrikaans  (2)
  20. Croatian  (1)
  21. More options open sub menu
INSPIRE LIBRARY - TON DUC THANG UNIVERSITY (84-028) 37 755 057 Feedback
19 Nguyen Huu Tho St. Dist.7, HCM thuvien@tdtu.edu.vn

Copyright © 2017 INSPIRE LIBRARY - TON DUC THANG UNIVERSITY

Searching Remote Databases, Please Wait