187 related articles for article (PubMed ID: 16240413)
1. Positron emission tomography methods with potential for increased understanding of mental retardation and developmental disabilities.
Sundaram SK; Chugani HT; Chugani DC
Ment Retard Dev Disabil Res Rev; 2005; 11(4):325-30. PubMed ID: 16240413
[TBL] [Abstract][Full Text] [Related]
2. Treatment of Neurogenetic Developmental Conditions: From 2016 into the Future.
van Karnebeek CD; Bowden K; Berry-Kravis E
Pediatr Neurol; 2016 Dec; 65():1-13. PubMed ID: 27697313
[TBL] [Abstract][Full Text] [Related]
3. Behavioral phenotypes in four mental retardation syndromes: fetal alcohol syndrome, Prader-Willi syndrome, fragile X syndrome, and tuberosis sclerosis.
Steinhausen HC; Von Gontard A; Spohr HL; Hauffa BP; Eiholzer U; Backes M; Willms J; Malin Z
Am J Med Genet; 2002 Sep; 111(4):381-7. PubMed ID: 12210296
[TBL] [Abstract][Full Text] [Related]
4. People with intellectual disability: what do we know about adulthood and life expectancy?
Coppus AM
Dev Disabil Res Rev; 2013; 18(1):6-16. PubMed ID: 23949824
[TBL] [Abstract][Full Text] [Related]
5. Positron Emission Tomography (PET) Quantification of GABAA Receptors in the Brain of Fragile X Patients.
D'Hulst C; Heulens I; Van der Aa N; Goffin K; Koole M; Porke K; Van De Velde M; Rooms L; Van Paesschen W; Van Esch H; Van Laere K; Kooy RF
PLoS One; 2015; 10(7):e0131486. PubMed ID: 26222316
[TBL] [Abstract][Full Text] [Related]
6. Rare diseases offer insights into autism spectrum disorders. Preliminary laboratory studies suggest new biological targets for intervention.
Harv Ment Health Lett; 2009 Apr; 25(10):3. PubMed ID: 19475765
[No Abstract] [Full Text] [Related]
7. Genetic and epigenetic dysregulation of imprinted genes in the brain.
Kernohan KD; Bérubé NG
Epigenomics; 2010 Dec; 2(6):743-63. PubMed ID: 22122080
[TBL] [Abstract][Full Text] [Related]
8. Emerging pharmacotherapies for neurodevelopmental disorders.
Wetmore DZ; Garner CC
J Dev Behav Pediatr; 2010 Sep; 31(7):564-81. PubMed ID: 20814256
[TBL] [Abstract][Full Text] [Related]
9. From molecules to behavior: lessons from the study of rare genetic disorders.
Roubertoux PL; de Vries PJ
Behav Genet; 2011 May; 41(3):341-8. PubMed ID: 21541644
[TBL] [Abstract][Full Text] [Related]
10. The Prader-Willi phenotype of fragile X syndrome.
Nowicki ST; Tassone F; Ono MY; Ferranti J; Croquette MF; Goodlin-Jones B; Hagerman RJ
J Dev Behav Pediatr; 2007 Apr; 28(2):133-8. PubMed ID: 17435464
[TBL] [Abstract][Full Text] [Related]
11. The GABAA Receptor as a Therapeutic Target for Neurodevelopmental Disorders.
Braat S; Kooy RF
Neuron; 2015 Jun; 86(5):1119-30. PubMed ID: 26050032
[TBL] [Abstract][Full Text] [Related]
12. Molecular genetics and animal models in autistic disorder.
Andres C
Brain Res Bull; 2002 Jan; 57(1):109-19. PubMed ID: 11827743
[TBL] [Abstract][Full Text] [Related]
13. New innovations: therapeutic opportunities for intellectual disabilities.
Picker JD; Walsh CA
Ann Neurol; 2013 Sep; 74(3):382-90. PubMed ID: 24038210
[TBL] [Abstract][Full Text] [Related]
14. Systematic Review: Emotion Dysregulation in Syndromic Causes of Intellectual and Developmental Disabilities.
Shaffer RC; Reisinger DL; Schmitt LM; Lamy M; Dominick KC; Smith EG; Coffman MC; Esbensen AJ
J Am Acad Child Adolesc Psychiatry; 2023 May; 62(5):518-557. PubMed ID: 36007813
[TBL] [Abstract][Full Text] [Related]
15. GABA A receptor abnormalities in Prader-Willi syndrome assessed with positron emission tomography and [11C]flumazenil.
Lucignani G; Panzacchi A; Bosio L; Moresco RM; Ravasi L; Coppa I; Chiumello G; Frey K; Koeppe R; Fazio F
Neuroimage; 2004 May; 22(1):22-8. PubMed ID: 15109994
[TBL] [Abstract][Full Text] [Related]
16. Temporal lobe dysfunction in childhood autism: a PET study. Positron emission tomography.
Zilbovicius M; Boddaert N; Belin P; Poline JB; Remy P; Mangin JF; Thivard L; Barthélémy C; Samson Y
Am J Psychiatry; 2000 Dec; 157(12):1988-93. PubMed ID: 11097965
[TBL] [Abstract][Full Text] [Related]
17. Features of autism in Rett syndrome and severe mental retardation.
Mount RH; Charman T; Hastings RP; Reilly S; Cass H
J Autism Dev Disord; 2003 Aug; 33(4):435-42. PubMed ID: 12959422
[TBL] [Abstract][Full Text] [Related]
18. Psychiatric features in children with genetic syndromes: toward functional phenotypes.
Siegel MS; Smith WE
Child Adolesc Psychiatr Clin N Am; 2010 Apr; 19(2):229-61, viii. PubMed ID: 20478498
[TBL] [Abstract][Full Text] [Related]
19. Recent experience with Rett syndrome at a tertiary care center.
Kumar S; Alexander M; Gnanamuthu C
Neurol India; 2004 Dec; 52(4):494-5. PubMed ID: 15626843
[TBL] [Abstract][Full Text] [Related]
20. Alterations of amino acids and monoamine metabolism in male Fmr1 knockout mice: a putative animal model of the human fragile X mental retardation syndrome.
Gruss M; Braun K
Neural Plast; 2001; 8(4):285-98. PubMed ID: 12018775
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
