384 related articles for article (PubMed ID: 18174548)
61. Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome.
Cuddapah VA; Pillai RB; Shekar KV; Lane JB; Motil KJ; Skinner SA; Tarquinio DC; Glaze DG; McGwin G; Kaufmann WE; Percy AK; Neul JL; Olsen ML
J Med Genet; 2014 Mar; 51(3):152-8. PubMed ID: 24399845
[TBL] [Abstract][Full Text] [Related]
62. [Rett syndrome: a diagnostic, clinical and molecular update].
Tejada MI
Rev Neurol; 2006 Jan; 42 Suppl 1():S55-9. PubMed ID: 16506134
[TBL] [Abstract][Full Text] [Related]
63. The diagnosis of autism in a female: could it be Rett syndrome?
Young DJ; Bebbington A; Anderson A; Ravine D; Ellaway C; Kulkarni A; de Klerk N; Kaufmann WE; Leonard H
Eur J Pediatr; 2008 Jun; 167(6):661-9. PubMed ID: 17684768
[TBL] [Abstract][Full Text] [Related]
64. [Molecular genetic study of MECP2 gene for a patient with typical Rett syndrome].
Zhu HY; Hu YL; Zhu RF; Yang Y; Zhu XY; Wang WJ; Duan HL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):625-9. PubMed ID: 22161092
[TBL] [Abstract][Full Text] [Related]
65. A novel MECP2 mutation in a boy with neonatal encephalopathy and facial dysmorphism.
Jülich K; Horn D; Burfeind P; Erler T; Auber B
J Pediatr; 2009 Jul; 155(1):140-3. PubMed ID: 19559301
[TBL] [Abstract][Full Text] [Related]
66. Early determinants of fractures in Rett syndrome.
Downs J; Bebbington A; Woodhead H; Jacoby P; Jian L; Jefferson A; Leonard H
Pediatrics; 2008 Mar; 121(3):540-6. PubMed ID: 18310203
[TBL] [Abstract][Full Text] [Related]
67. Gene symbol: MECP2. Disease: Rett syndrome.
Zahorakova D; Jüttnerova V; Zeman J; Martasek P
Hum Genet; 2008 Oct; 124(3):315. PubMed ID: 18846663
[No Abstract] [Full Text] [Related]
68. Mutation screening of the MECP2 gene in a large cohort of 613 fragile-X negative patients with mental retardation.
Lesca G; Bernard V; Bozon M; Touraine R; Gérard D; Edery P; Calender A
Eur J Med Genet; 2007; 50(3):200-8. PubMed ID: 17383248
[TBL] [Abstract][Full Text] [Related]
69. Epilepsy in Rett syndrome--lessons from the Rett networked database.
Nissenkorn A; Levy-Drummer RS; Bondi O; Renieri A; Villard L; Mari F; Mencarelli MA; Lo Rizzo C; Meloni I; Pineda M; Armstrong J; Clarke A; Bahi-Buisson N; Mejaski BV; Djuric M; Craiu D; Djukic A; Pini G; Bisgaard AM; Melegh B; Vignoli A; Russo S; Anghelescu C; Veneselli E; Hayek J; Ben-Zeev B
Epilepsia; 2015 Apr; 56(4):569-76. PubMed ID: 25789914
[TBL] [Abstract][Full Text] [Related]
70. InterRett--The application of bioinformatics to International Rett syndrome research.
Moore H; Leonard H; Fyfe S; De Klerk N; Leonard N
Ann Hum Biol; 2005; 32(2):228-36. PubMed ID: 16096221
[TBL] [Abstract][Full Text] [Related]
71. Environmental enrichment ameliorates a motor coordination deficit in a mouse model of Rett syndrome--Mecp2 gene dosage effects and BDNF expression.
Kondo M; Gray LJ; Pelka GJ; Christodoulou J; Tam PP; Hannan AJ
Eur J Neurosci; 2008 Jun; 27(12):3342-50. PubMed ID: 18557922
[TBL] [Abstract][Full Text] [Related]
72. Acquired microcephaly, regression of milestones, mitochondrial dysfunction, and episodic rigidity in a 46,XY male with a de novo MECP2 gene mutation.
Condie J; Goldstein J; Wainwright MS
J Child Neurol; 2010 May; 25(5):633-6. PubMed ID: 20142466
[TBL] [Abstract][Full Text] [Related]
73. Comparative study of brain morphology in Mecp2 mutant mouse models of Rett syndrome.
Belichenko NP; Belichenko PV; Li HH; Mobley WC; Francke U
J Comp Neurol; 2008 May; 508(1):184-95. PubMed ID: 18306326
[TBL] [Abstract][Full Text] [Related]
74. The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndrome.
Nectoux J; Bahi-Buisson N; Guellec I; Coste J; De Roux N; Rosas H; Tardieu M; Chelly J; Bienvenu T
Neurology; 2008 May; 70(22 Pt 2):2145-51. PubMed ID: 18434641
[TBL] [Abstract][Full Text] [Related]
75. Mutations found within exon 1 of MECP2 in Danish patients with Rett syndrome.
Ravn K; Nielsen JB; Schwartz M
Clin Genet; 2005 Jun; 67(6):532-3. PubMed ID: 15857422
[No Abstract] [Full Text] [Related]
76. Atypical features in MECP2 P152R-associated Rett syndrome.
Sheen V; Valencia IM; Torres AR
Pediatr Neurol; 2013 Aug; 49(2):124-6. PubMed ID: 23859859
[TBL] [Abstract][Full Text] [Related]
77. MECP2 mutation in one of Rett's original patients.
Freilinger M; Berndt A; Haas OA
J Med Genet; 2009 Sep; 46(9):647-8. PubMed ID: 19724012
[No Abstract] [Full Text] [Related]
78. Longevity in Rett syndrome: analysis of the North American Database.
Kirby RS; Lane JB; Childers J; Skinner SA; Annese F; Barrish JO; Glaze DG; Macleod P; Percy AK
J Pediatr; 2010 Jan; 156(1):135-138.e1. PubMed ID: 19772971
[TBL] [Abstract][Full Text] [Related]
79. Gene symbol: MECP2. Disease: Rett syndrome.
Sprovieri T; Mazzei R; Ungaro C; Citrigno L; Quattrone A; Conforti FL
Hum Genet; 2008 Jun; 123(5):555. PubMed ID: 20960664
[No Abstract] [Full Text] [Related]
80. Targeted delivery of an Mecp2 transgene to forebrain neurons improves the behavior of female Mecp2-deficient mice.
Jugloff DG; Vandamme K; Logan R; Visanji NP; Brotchie JM; Eubanks JH
Hum Mol Genet; 2008 May; 17(10):1386-96. PubMed ID: 18223199
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]