129 related articles for article (PubMed ID: 33168794)
1. Methyl-CpG-binding protein 2 gene mutations and its association with epilepsy: a single centre study from the Indian subcontinent.
Kamdar P; Thomas M; Yoganathan S; Muthusamy K; Koshy B; Philip Oommen S; Aaron R; Barney A; Susan C Abraham S; Danda S
J Genet; 2020; 99():. PubMed ID: 33168794
[TBL] [Abstract][Full Text] [Related]
2. MECP2 mutation spectrum and its clinical characteristics in a Chinese cohort.
Wen Y; Wang J; Zhang Q; Chen Y; Wu X; Bao X
Clin Genet; 2020 Sep; 98(3):240-250. PubMed ID: 32472557
[TBL] [Abstract][Full Text] [Related]
3. Mutational analysis of methyl-CpG binding protein 2 (MECP2) gene in Indian cases of Rett syndrome.
Das DK; Udani V; Sanghavi D; Adhia R; Maitra A
J Clin Lab Anal; 2013 Mar; 27(2):137-42. PubMed ID: 23400946
[TBL] [Abstract][Full Text] [Related]
4. MECP2 mutations in Czech patients with Rett syndrome and Rett-like phenotypes: novel mutations, genotype-phenotype correlations and validation of high-resolution melting analysis for mutation scanning.
Zahorakova D; Lelkova P; Gregor V; Magner M; Zeman J; Martasek P
J Hum Genet; 2016 Jul; 61(7):617-25. PubMed ID: 26984561
[TBL] [Abstract][Full Text] [Related]
5. Genotype-phenotype relationship among Egyptian children with Rett syndrome.
Mansour L; El Sobky E; Mohamed SM; Marzouk H; Tarek LA
J Egypt Public Health Assoc; 2015 Sep; 90(3):133-7. PubMed ID: 26544843
[TBL] [Abstract][Full Text] [Related]
6. Spectrum of MECP2 mutations in Vietnamese patients with RETT syndrome.
Le Thi Thanh H; Do Thi Diem T; Duy CV; Thanh HLT; Phuong HBT; Thanh LN
BMC Med Genet; 2018 Aug; 19(1):137. PubMed ID: 30081849
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Spectrum of MECP2 gene mutations in a cohort of Indian patients with Rett syndrome: report of two novel mutations.
Das DK; Raha S; Sanghavi D; Maitra A; Udani V
Gene; 2013 Feb; 515(1):78-83. PubMed ID: 23262346
[TBL] [Abstract][Full Text] [Related]
9. [Mutation spectrum and genotype-phenotype correlation of MECP2 in patients with Rett syndrome].
Kondo I; Yamagata H
No To Hattatsu; 2002 May; 34(3):219-23. PubMed ID: 12030010
[TBL] [Abstract][Full Text] [Related]
10. Surface- and voxel-based brain morphologic study in Rett and Rett-like syndrome with MECP2 mutation.
Shiohama T; Levman J; Takahashi E
Int J Dev Neurosci; 2019 Apr; 73():83-88. PubMed ID: 30690146
[TBL] [Abstract][Full Text] [Related]
11. MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disorders.
Psoni S; Sofocleous C; Traeger-Synodinos J; Kitsiou-Tzeli S; Kanavakis E; Fryssira-Kanioura H
Brain Dev; 2012 Jun; 34(6):487-95. PubMed ID: 21982064
[TBL] [Abstract][Full Text] [Related]
12. [Application of long range polymerase chain reaction and DNA direct sequencing in diagnosis of Rett syndrome].
Li MR; Pan H; Bao XH; Cao GN; Wu XR
Zhonghua Er Ke Za Zhi; 2007 Aug; 45(8):579-82. PubMed ID: 18021529
[TBL] [Abstract][Full Text] [Related]
13. Brief report: MECP2 mutations in people without Rett syndrome.
Suter B; Treadwell-Deering D; Zoghbi HY; Glaze DG; Neul JL
J Autism Dev Disord; 2014 Mar; 44(3):703-11. PubMed ID: 23921973
[TBL] [Abstract][Full Text] [Related]
14. Drug-resistant epilepsy and epileptic phenotype-EEG association in MECP2 mutated Rett syndrome.
Buoni S; Zannolli R; Felice CD; Saponari S; Strambi M; Dotti MT; Castrucci E; Corbini L; Orsi A; Hayek J
Clin Neurophysiol; 2008 Nov; 119(11):2455-8. PubMed ID: 18842453
[TBL] [Abstract][Full Text] [Related]
15. MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome.
Li MR; Pan H; Bao XH; Zhang YZ; Wu XR
J Hum Genet; 2007; 52(1):38-47. PubMed ID: 17089071
[TBL] [Abstract][Full Text] [Related]
16. Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations.
Hadzsiev K; Polgar N; Bene J; Komlosi K; Karteszi J; Hollody K; Kosztolanyi G; Renieri A; Melegh B
J Hum Genet; 2011 Mar; 56(3):183-7. PubMed ID: 21160487
[TBL] [Abstract][Full Text] [Related]
17. Epilepsy in Rett syndrome---the experience of a National Rett Center.
Nissenkorn A; Gak E; Vecsler M; Reznik H; Menascu S; Ben Zeev B
Epilepsia; 2010 Jul; 51(7):1252-8. PubMed ID: 20491871
[TBL] [Abstract][Full Text] [Related]
18. Genetic and clinical variations in a Norwegian sample diagnosed with Rett syndrome.
Henriksen MW; Breck H; Sejersted Y; Diseth T; von Tetzchner S; Paus B; Skjeldal OH
Brain Dev; 2020 Aug; 42(7):484-495. PubMed ID: 32336485
[TBL] [Abstract][Full Text] [Related]
19. Circulating 4-F
Signorini C; Leoncini S; Durand T; Galano JM; Guy A; Bultel-Poncé V; Oger C; Lee JC; Ciccoli L; Hayek J; De Felice C
Int J Mol Sci; 2021 Apr; 22(8):. PubMed ID: 33921863
[TBL] [Abstract][Full Text] [Related]
20. Two novel mutations in the MECP2 gene in patients with Rett syndrome.
Khalili Alashti S; Fallahi J; Mohammadi S; Dehghanian F; Farbood Z; Masoudi M; Poorang S; Jokar A; Fardaei M
Gene; 2020 Mar; 732():144337. PubMed ID: 31958484
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]