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Items: 1 to 20 of 85

1.
Using the Recovery Capital Model to Explore Barriers to and Facilitators of Recovery in Individuals with Substance Use Disorder, Psychiatric Comorbidity and Mild-to-Borderline Intellectual Disability: A Case Series
Esther Pars, Joanne E. L. VanDerNagel, Boukje A. G. Dijkstra, Arnt F. A. Schellekens
J Clin Med. 2023 Sep; 12(18): 5914. Published online 2023 Sep 12. doi: 10.3390/jcm12185914
PMCID:
PMC10531644
ArticlePDF–251K
2.
Development of an Alcohol Refusal Training in Immersive Virtual Reality for Patients With Mild to Borderline Intellectual Disability and Alcohol Use Disorder: Cocreation With Experts in Addiction Care
Simon Langener, Jan Kolkmeier, Joanne VanDerNagel, Randy Klaassen, Jeannette van Manen, Dirk Heylen
JMIR Form Res. 2023; 7: e42523. Published online 2023 Apr 26. doi: 10.2196/42523
PMCID:
PMC10173034
ArticlePDF–1.9M
3.
Immersive Virtual Reality Avatars for Embodiment Illusions in People With Mild to Borderline Intellectual Disability: User-Centered Development and Feasibility Study
Simon Langener, Randy Klaassen, Joanne VanDerNagel, Dirk Heylen
JMIR Serious Games. 2022 Oct-Dec; 10(4): e39966. Published online 2022 Dec 7. doi: 10.2196/39966
PMCID:
PMC9773028
Article
4.
Case Report: A Novel Point Mutation of SOX3 in a Subject With Growth Hormone Deficiency, Hypogonadotrophic Hypogonadism, and Borderline Intellectual Disability
Jing Li, Yuxia Zhong, Tao Guo, Yerong Yu, Jianwei Li
Front Endocrinol (Lausanne) 2022; 13: 810375. Published online 2022 Feb 28. doi: 10.3389/fendo.2022.810375
PMCID:
PMC8918540
ArticlePDF–2.2M
5.
Substance use problems among people with mild/borderline intellectual disability: Challenges to mainstream multidisciplinary specialist substance treatment in Norway
Anne Juberg, Monica Røstad, Erik Søndenaa
Nordisk Alkohol Nark. 2017 Apr; 34(2): 173–185. Published online 2017 Mar 23. doi: 10.1177/1455072516687255
PMCID:
PMC7450860
ArticlePDF–229K
6.
Executive Functions and Emotion Regulation in Attention-Deficit/Hyperactivity Disorder and Borderline Intellectual Disability
Elena Predescu, Roxana Sipos, Cristina A. Costescu, Anamaria Ciocan, Diana I. Rus
J Clin Med. 2020 Apr; 9(4): 986. Published online 2020 Apr 1. doi: 10.3390/jcm9040986
PMCID:
PMC7231040
ArticlePDF–279K
7.
When Do those “Risk-Taking Adolescents” Take Risks? The Combined Effects of Risk Encouragement by Peers, Mild-to-Borderline Intellectual Disability and Sex
Eline Wagemaker, Hilde M. Huizenga, Tycho J. Dekkers, Annematt L. Collot d’Escury-Koenigs, Elske Salemink, Anika Bexkens
J Abnorm Child Psychol. 2020; 48(4): 573–587. Published online 2020 Jan 17. doi: 10.1007/s10802-020-00617-8
PMCID:
PMC7078137
ArticlePDF–614K
8.
A Systematic Review of Substance Use (Disorder) in Individuals with Mild to Borderline Intellectual Disability
Neomi van Duijvenbode, Joanne E.L. VanDerNagel
Eur Addict Res. 2019 Nov; 25(6): 263–282. Published online 2019 Jul 22. doi: 10.1159/000501679
PMCID:
PMC6888885
Article
9.
Formal Modeling of the Resistance to Peer Influence Questionnaire: A Comparison of Adolescent Boys and Girls With and Without Mild-to-Borderline Intellectual Disability
Laura M. S. Dekkers, Anika Bexkens, Abe D. Hofman, Paul De Boeck, Annematt L. Collot d’Escury, Hilde M. Huizenga
Assessment. 2019 Sep; 26(6): 1070–1083. Published online 2017 Mar 23. doi: 10.1177/1073191117698754
PMCID:
PMC6696739
ArticlePDF–524K
10.
A boy with conduct disorder (CD), attention deficit hyperactivity disorder (ADHD), borderline intellectual disability, and 47,XXY syndrome in combination with a 7q11.23 duplication, 11p15.5 deletion, and 20q13.33 deletion
Gerasimos Kolaitis, Christian G. Bouwkamp, Alexia Papakonstantinou, Ioanna Otheiti, Maria Belivanaki, Styliani Haritaki, Terpsihori Korpa, Zinovia Albani, Elena Terzioglou, Polyxeni Apostola, Aggeliki Skamnaki, Athena Xaidara, Konstantina Kosma, Sophia Kitsiou-Tzeli, Maria Tzetis
Child Adolesc Psychiatry Ment Health. 2016; 10: 33. Published online 2016 Sep 15. doi: 10.1186/s13034-016-0121-8
PMCID:
PMC5024517
ArticlePDF–1.7M
11.
Cool Decision-Making in Adolescents with Behavior Disorder and/or Mild-to-Borderline Intellectual Disability
Anika Bexkens, Brenda R. J. Jansen, Maurits W. Van der Molen, Hilde M. Huizenga
J Abnorm Child Psychol. 2016; 44(2): 357–367. Published online 2015 Mar 20. doi: 10.1007/s10802-015-9996-8
PMCID:
PMC4729804
ArticlePDF–518K
12.
Genetic Dysruption of the Histaminergic Pathways: A Novel Deletion at the 15q21.2 locus Associated with Variable Expressivity of Neuropsychiatric Disorders
Carla Lintas, Roberto Sacco, Alessia Azzarà, Ilaria Cassano, Luigi Laino, Paola Grammatico, Fiorella Gurrieri
Genes (Basel) 2022 Oct; 13(10): 1685. Published online 2022 Sep 20. doi: 10.3390/genes13101685
PMCID:
PMC9602325
ArticlePDF–810K
13.
De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disability
Iris G. M. Wijnen, Hermine E. Veenstra-Knol, Fleur Vansenne, Erica H. Gerkes, Tom de Koning, Yvonne J. Vos, Marina A. J. Tijssen, Deborah Sival, Niklas Darin, Els K. Vanhoutte, Mayke Oosterloo, Maartje Pennings, Bart P. van de Warrenburg, Erik-Jan Kamsteeg
Eur J Hum Genet. 2020 Jun; 28(6): 763–769. Published online 2020 Mar 10. doi: 10.1038/s41431-020-0600-5
PMCID:
PMC7253440
ArticlePDF–647K
14.
Concurrent pathogenic variants in SLC6A1/NOTCH1/PRIMPOL genes in a Chinese patient with myoclonic-atonic epilepsy, mild aortic valve stenosis and high myopia
Haiming Yuan, Qingming Wang, Yufeng Li, Shuangxi Cheng, Jianxin Liu, Yanhui Liu
BMC Med Genet. 2020; 21: 93. Published online 2020 May 6. doi: 10.1186/s12881-020-01035-9
PMCID:
PMC7203802
ArticlePDF–730K
15.
The use of two different MLPA kits in 22q11.2 Deletion Syndrome
L.J.M. Evers, J.J.M. Engelen, L.M.H. Houben, L.M.G. Curfs, T.A.M.J. van Amelsvoort
Eur J Med Genet. Author manuscript; available in PMC 2017 Apr 1.
Published in final edited form as: Eur J Med Genet. 2016 Apr; 59(4): 183–188. Published online 2016 Feb 24. doi: 10.1016/j.ejmg.2016.02.009
PMCID:
PMC4820537
ArticlePDF–777K
16.
Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatellite
Avinash V Dharmadhikari, Tomasz Gambin, Przemyslaw Szafranski, Wenjian Cao, Frank J Probst, Weihong Jin, Ping Fang, Krzysztof Gogolewski, Anna Gambin, Jaya K George-Abraham, Sailaja Golla, Francoise Boidein, Benedicte Duban-Bedu, Bruno Delobel, Joris Andrieux, Kerstin Becker, Elke Holinski-Feder, Sau Wai Cheung, Pawel Stankiewicz
BMC Med Genet. 2014; 15: 128. Published online 2014 Dec 4. doi: 10.1186/s12881-014-0128-z
PMCID:
PMC4411736
ArticlePDF–2.6M
17.
Neurodevelopmental disorders among individuals with duplication of 4p13 to 4p12 containing a GABAA receptor subunit gene cluster
Michelle B Polan, Matthew T Pastore, Katherine Steingass, Sayaka Hashimoto, Devon L Thrush, Robert Pyatt, Shalini Reshmi, Julie M Gastier-Foster, Caroline Astbury, Kim L McBride
Eur J Hum Genet. 2014 Jan; 22(1): 105–109. Published online 2013 May 22. doi: 10.1038/ejhg.2013.99
PMCID:
PMC3865421
ArticlePDF–830K
18.
Haploinsufficiency of CELF4 at 18q12.2 is associated with developmental and behavioral disorders, seizures, eye manifestations, and obesity
Christina Halgren, Iben Bache, Mads Bak, Mikkel Wanting Myatt, Claire Marie Anderson, Karen Brøndum-Nielsen, Niels Tommerup
Eur J Hum Genet. 2012 Dec; 20(12): 1315–1319. Published online 2012 May 23. doi: 10.1038/ejhg.2012.92
PMCID:
PMC3499750
ArticlePDF–554K
19.
A Homozygous NDUFS6 Variant Associated with Neuropathy and Optic Atrophy
Andrea Gangfuß, Philipp Rating, Tomas Ferreira, Andreas Hentschel, Adela Della Marina, Heike Kölbel, Albert Sickmann, Angela Abicht, Florian Kraft, Tobias Ruck, Johann Böhm, Anne Schänzer, Ulrike Schara-Schmidt, Teresa M. Neuhann, Rita Horvath, Andreas Roos
J Neuromuscul Dis. 2024; 11(2): 485–491. Prepublished online 2024 Jan 8. Published online 2024 Mar 5. doi: 10.3233/JND-230181
PMCID:
PMC10977349
ArticlePDF–405K
20.
Genotype-phenotype correlation of deletions and duplications of 4p: case reports and literature review
Xuan Zhang, Hongjuan Lu, Hanran Yang, Yichen Ji, Huixin Liu, Wenjian Liu, Jiayi Li, Zhixian Yang, Wei Sun
Front Genet. 2023; 14: 1174314. Published online 2023 Jun 14. doi: 10.3389/fgene.2023.1174314
PMCID:
PMC10300434
ArticlePDF–1.1M

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