161 related articles for article (PubMed ID: 16288669)
1. Attention deficits in children with 22q.11 deletion syndrome.
Niklasson L; Rasmussen P; Oskarsdóttir S; Gillberg C
Dev Med Child Neurol; 2005 Dec; 47(12):803-7. PubMed ID: 16288669
[TBL] [Abstract][Full Text] [Related]
2. Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome.
Niklasson L; Rasmussen P; Oskarsdóttir S; Gillberg C
Res Dev Disabil; 2009; 30(4):763-73. PubMed ID: 19070990
[TBL] [Abstract][Full Text] [Related]
3. Memory and learning in children with 22q11.2 deletion syndrome: evidence for ventral and dorsal stream disruption?
Lajiness-O'Neill RR; Beaulieu I; Titus JB; Asamoah A; Bigler ED; Bawle EV; Pollack R
Child Neuropsychol; 2005 Feb; 11(1):55-71. PubMed ID: 15823983
[TBL] [Abstract][Full Text] [Related]
4. The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.
Swillen A; Devriendt K; Legius E; Prinzie P; Vogels A; Ghesquière P; Fryns JP
Genet Couns; 1999; 10(1):79-88. PubMed ID: 10191433
[TBL] [Abstract][Full Text] [Related]
5. Learning disabilities in children with neurofibromatosis type 1: subtypes, cognitive profile, and attention-deficit-hyperactivity disorder.
Hyman SL; Arthur Shores E; North KN
Dev Med Child Neurol; 2006 Dec; 48(12):973-7. PubMed ID: 17109785
[TBL] [Abstract][Full Text] [Related]
6. Neuropsychological, learning and psychosocial profile of primary school aged children with the velo-cardio-facial syndrome (22q11 deletion): evidence for a nonverbal learning disability?
Swillen A; Vandeputte L; Cracco J; Maes B; Ghesquière P; Devriendt K; Fryns JP
Child Neuropsychol; 1999 Dec; 5(4):230-41. PubMed ID: 10925707
[TBL] [Abstract][Full Text] [Related]
7. Atypical neuropsychological profile in a boy with 22q11.2 Deletion Syndrome.
Stiers P; Swillen A; De Smedt B; Lagae L; Devriendt K; D'Agostino E; Sunaert S; Fryns AP
Child Neuropsychol; 2005 Feb; 11(1):87-108. PubMed ID: 15823985
[TBL] [Abstract][Full Text] [Related]
8. The neuropsychology of 22q11 deletion syndrome. A neuropsychiatric study of 100 individuals.
Niklasson L; Gillberg C
Res Dev Disabil; 2010; 31(1):185-94. PubMed ID: 19815377
[TBL] [Abstract][Full Text] [Related]
9. Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome.
Shashi V; Keshavan MS; Howard TD; Berry MN; Basehore MJ; Lewandowski E; Kwapil TR
Clin Genet; 2006 Mar; 69(3):234-8. PubMed ID: 16542388
[TBL] [Abstract][Full Text] [Related]
10. Core neuropsychological characteristics of children and adolescents with 22q11.2 deletion.
Jacobson C; Shearer J; Habel A; Kane F; Tsakanikos E; Kravariti E
J Intellect Disabil Res; 2010 Aug; 54(8):701-13. PubMed ID: 20561146
[TBL] [Abstract][Full Text] [Related]
11. Motor development in school-aged children with 22q11 deletion (velocardiofacial/DiGeorge syndrome).
Van Aken K; De Smedt B; Van Roie A; Gewillig M; Devriendt K; Fryns JP; Simons J; Swillen A
Dev Med Child Neurol; 2007 Mar; 49(3):210-3. PubMed ID: 17355478
[TBL] [Abstract][Full Text] [Related]
12. The neurocognitive phenotype in velo-cardio-facial syndrome: a developmental perspective.
Antshel KM; Fremont W; Kates WR
Dev Disabil Res Rev; 2008; 14(1):43-51. PubMed ID: 18636636
[TBL] [Abstract][Full Text] [Related]
13. The impact of sex and subtypes on cognitive and psychosocial aspects of ADHD.
Gross-Tsur V; Goldzweig G; Landau YE; Berger I; Shmueli D; Shalev RS
Dev Med Child Neurol; 2006 Nov; 48(11):901-5. PubMed ID: 17044958
[TBL] [Abstract][Full Text] [Related]
14. Neuropsychological functioning in girls with attention-deficit/hyperactivity disorder with and without learning disabilities.
Seidman LJ; Biederman J; Valera EM; Monuteaux MC; Doyle AE; Faraone SV
Neuropsychology; 2006 Mar; 20(2):166-77. PubMed ID: 16594777
[TBL] [Abstract][Full Text] [Related]
15. The neurocognitive phenotype of the 22q11.2 deletion syndrome: selective deficit in visual-spatial memory.
Bearden CE; Woodin MF; Wang PP; Moss E; McDonald-McGinn D; Zackai E; Emannuel B; Cannon TD
J Clin Exp Neuropsychol; 2001 Aug; 23(4):447-64. PubMed ID: 11780945
[TBL] [Abstract][Full Text] [Related]
16. Developmental right-hemisphere syndrome: clinical spectrum of the nonverbal learning disability.
Gross-Tsur V; Shalev RS; Manor O; Amir N
J Learn Disabil; 1995 Feb; 28(2):80-6. PubMed ID: 7884301
[TBL] [Abstract][Full Text] [Related]
17. Support for an independent familial segregation of executive and intelligence endophenotypes in ADHD families.
Rommelse NN; Altink ME; Oosterlaan J; Buschgens CJ; Buitelaar J; Sergeant JA
Psychol Med; 2008 Nov; 38(11):1595-606. PubMed ID: 18261248
[TBL] [Abstract][Full Text] [Related]
18. Memory in intellectually matched groups of young participants with 22q11.2 deletion syndrome and those with schizophrenia.
Kravariti E; Jacobson C; Morris R; Frangou S; Murray RM; Tsakanikos E; Habel A; Shearer J
Res Dev Disabil; 2010; 31(3):864-8. PubMed ID: 20307954
[TBL] [Abstract][Full Text] [Related]
19. [A neuropsychological and behavioural profile of attention deficits in fragile X syndrome].
Cornish K; Munir F; Wilding J
Rev Neurol; 2001 Oct; 33 Suppl 1():S24-9. PubMed ID: 12447815
[TBL] [Abstract][Full Text] [Related]
20. Neuropsychiatric and neurodevelopmental outcome of children at age 6 and 7 years who screened positive for language problems at 30 months.
Miniscalco C; Nygren G; Hagberg B; Kadesjö B; Gillberg C
Dev Med Child Neurol; 2006 May; 48(5):361-6. PubMed ID: 16608544
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]