These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
179 related articles for article (PubMed ID: 12112730)
1. Neuropathology of Rett syndrome. Armstrong DD Ment Retard Dev Disabil Res Rev; 2002; 8(2):72-6. PubMed ID: 12112730 [TBL] [Abstract][Full Text] [Related]
4. Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype. Hoffbuhr KC; Moses LM; Jerdonek MA; Naidu S; Hoffman EP Ment Retard Dev Disabil Res Rev; 2002; 8(2):99-105. PubMed ID: 12112735 [TBL] [Abstract][Full Text] [Related]
5. Severe congenital encephalopathy caused by MECP2 null mutations in males: central hypoxia and reduced neuronal dendritic structure. Schüle B; Armstrong DD; Vogel H; Oviedo A; Francke U Clin Genet; 2008 Aug; 74(2):116-26. PubMed ID: 18477000 [TBL] [Abstract][Full Text] [Related]
6. Neuroanatomy of Rett syndrome: a volumetric imaging study. Reiss AL; Faruque F; Naidu S; Abrams M; Beaty T; Bryan RN; Moser H Ann Neurol; 1993 Aug; 34(2):227-34. PubMed ID: 8338347 [TBL] [Abstract][Full Text] [Related]
7. Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patients. Santos M; Temudo T; Kay T; Carrilho I; Medeira A; Cabral H; Gomes R; Lourenço MT; Venâncio M; Calado E; Moreira A; Oliveira G; Maciel P J Child Neurol; 2009 Jan; 24(1):49-55. PubMed ID: 19168818 [TBL] [Abstract][Full Text] [Related]
8. Neuropathology of Rett syndrome. Armstrong DD J Child Neurol; 2005 Sep; 20(9):747-53. PubMed ID: 16225830 [TBL] [Abstract][Full Text] [Related]
9. Quantitative magnetic resonance imaging and studies of degenerative diseases of the developing human brain. Caviness VS; Filipek PA; Kennedy DN Brain Dev; 1992 May; 14 Suppl():S80-5. PubMed ID: 1626638 [TBL] [Abstract][Full Text] [Related]
10. Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks. Belichenko PV; Wright EE; Belichenko NP; Masliah E; Li HH; Mobley WC; Francke U J Comp Neurol; 2009 May; 514(3):240-58. PubMed ID: 19296534 [TBL] [Abstract][Full Text] [Related]
11. The neuropathology of Rett syndrome--overview 1994. Armstrong DD Neuropediatrics; 1995 Apr; 26(2):100-4. PubMed ID: 7566445 [TBL] [Abstract][Full Text] [Related]
12. Rett syndrome: prevalence among Chinese and a comparison of MECP2 mutations of classic Rett syndrome with other neurodevelopmental disorders. Wong VC; Li SY J Child Neurol; 2007 Dec; 22(12):1397-400. PubMed ID: 18174559 [TBL] [Abstract][Full Text] [Related]
13. The neuropathology of the Rett syndrome. Armstrong DD Brain Dev; 1992 May; 14 Suppl():S89-98. PubMed ID: 1626639 [TBL] [Abstract][Full Text] [Related]
14. Can we relate MeCP2 deficiency to the structural and chemical abnormalities in the Rett brain? Armstrong DD Brain Dev; 2005 Nov; 27 Suppl 1():S72-S76. PubMed ID: 16182497 [TBL] [Abstract][Full Text] [Related]
15. [Rett syndrome: clinical and molecular aspects]. Záhoráková D; Zeman J; Martásek P Cas Lek Cesk; 2007; 146(8):647-52. PubMed ID: 17874730 [TBL] [Abstract][Full Text] [Related]
16. Genetic basis of Rett syndrome. Van den Veyver IB; Zoghbi HY Ment Retard Dev Disabil Res Rev; 2002; 8(2):82-6. PubMed ID: 12112732 [TBL] [Abstract][Full Text] [Related]
17. Behavioral and anatomical abnormalities in Mecp2 mutant mice: a model for Rett syndrome. Stearns NA; Schaevitz LR; Bowling H; Nag N; Berger UV; Berger-Sweeney J Neuroscience; 2007 May; 146(3):907-21. PubMed ID: 17383101 [TBL] [Abstract][Full Text] [Related]
18. Rett syndrome: a prototypical neurodevelopmental disorder. Neul JL; Zoghbi HY Neuroscientist; 2004 Apr; 10(2):118-28. PubMed ID: 15070486 [TBL] [Abstract][Full Text] [Related]
19. Rett syndrome: 3-D confocal microscopy of cortical pyramidal dendrites and afferents. Belichenko PV; Oldfors A; Hagberg B; Dahlström A Neuroreport; 1994 Jul; 5(12):1509-13. PubMed ID: 7948850 [TBL] [Abstract][Full Text] [Related]
20. [Developmental disorder in girls due to Rett syndrome]. Pruissen DM; Sinke RJ; Terhal PA; Beemer FA; Peters AC Ned Tijdschr Geneeskd; 2003 Aug; 147(32):1560-3. PubMed ID: 12942847 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]