165 related articles for article (PubMed ID: 16607827)
1. [Considerations regarding one particular case of Rett syndrome].
Sireteanu A; Rusu C; Anton D; Covic M
Rev Med Chir Soc Med Nat Iasi; 2005; 109(1):50-2. PubMed ID: 16607827
[TBL] [Abstract][Full Text] [Related]
2. Rett syndrome: photographic evidence of rapid regression.
Fiumara A; Barone R; D'Asero G; Marzullo E; Pavone L
J Child Neurol; 1999 Aug; 14(8):550-2. PubMed ID: 10456770
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. MeCP2 dysfunction in Rett syndrome and related disorders.
Moretti P; Zoghbi HY
Curr Opin Genet Dev; 2006 Jun; 16(3):276-81. PubMed ID: 16647848
[TBL] [Abstract][Full Text] [Related]
5. Phenotypic and genotypic variability in four males with MECP2 gene sequence aberrations including a novel deletion.
Psoni S; Sofocleous C; Traeger-Synodinos J; Kitsiou-Tzeli S; Kanavakis E; Fryssira-Kanioura H
Pediatr Res; 2010 May; 67(5):551-6. PubMed ID: 20098342
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. Syndrome of microcephaly, mental retardation, and tracheoesophageal fistula associated with features of Rett syndrome.
Shetty AK; Chatters R; Tilton AH; Lacassie Y
J Child Neurol; 2000 Jan; 15(1):61-3. PubMed ID: 10641614
[TBL] [Abstract][Full Text] [Related]
8. Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome.
Meins M; Lehmann J; Gerresheim F; Herchenbach J; Hagedorn M; Hameister K; Epplen JT
J Med Genet; 2005 Feb; 42(2):e12. PubMed ID: 15689435
[No Abstract] [Full Text] [Related]
9. Molecular screening of MECP2 gene in a cohort of Lebanese patients suspected with Rett syndrome: report on a mild case with a novel indel mutation.
Corbani S; Chouery E; Fayyad J; Fawaz A; El Tourjuman O; Badens C; Lacoste C; Delague V; Megarbane A
J Intellect Disabil Res; 2012 Apr; 56(4):415-20. PubMed ID: 21954873
[TBL] [Abstract][Full Text] [Related]
10. [Subchromosomal microdeletion identified by molecular karyotyping using DNA microarrays (array CGH) in Rett syndrome girls negative for MECP2 gene mutations].
Vorsanova SG; Iurov IIu; Voinova VIu; Kurinnaia OS; Zelenova MA; Demidova IA; Ulas EV; Iurov IuB
Zh Nevrol Psikhiatr Im S S Korsakova; 2013; 113(10):63-8. PubMed ID: 24300809
[TBL] [Abstract][Full Text] [Related]
11. Social impairments in Rett syndrome: characteristics and relationship with clinical severity.
Kaufmann WE; Tierney E; Rohde CA; Suarez-Pedraza MC; Clarke MA; Salorio CF; Bibat G; Bukelis I; Naram D; Lanham DC; Naidu S
J Intellect Disabil Res; 2012 Mar; 56(3):233-47. PubMed ID: 21385260
[TBL] [Abstract][Full Text] [Related]
12. Congenital variant of Rett syndrome due to an intragenic large deletion in MECP2.
Kobayashi Y; Ohashi T; Akasaka N; Tohyama J
Brain Dev; 2012 Aug; 34(7):601-4. PubMed ID: 22001500
[TBL] [Abstract][Full Text] [Related]
13. Autistic disorder symptoms in Rett syndrome.
Wulffaert J; Van Berckelaer-Onnes IA; Scholte EM
Autism; 2009 Nov; 13(6):567-81. PubMed ID: 19933764
[TBL] [Abstract][Full Text] [Related]
14. Spectrum of MECP2 mutations in New Zealand Rett syndrome patients.
Raizis AM; Saleem M; MacKay R; George PM
N Z Med J; 2009 Jun; 122(1296):21-8. PubMed ID: 19652677
[TBL] [Abstract][Full Text] [Related]
15. [Clinical and molecular genetic findings in four girls with Rett syndrome].
Deutscher K; Deutscher J; Bergmann L; Tefs K; Reichwald K; Schuster V
Klin Padiatr; 2002; 214(5):291-4. PubMed ID: 12235545
[TBL] [Abstract][Full Text] [Related]
16. Novel de novo nonsense mutation of MECP2 in a patient with Rett syndrome.
Kim SJ; Cook EH
Hum Mutat; 2000 Apr; 15(4):382-3. PubMed ID: 10737989
[TBL] [Abstract][Full Text] [Related]
17. [Rett syndrome].
Schwartzman JS
Arq Neuropsiquiatr; 2007 Jun; 65(2B):544; author reply 544-5. PubMed ID: 17665035
[No Abstract] [Full Text] [Related]
18. Classical Rett Syndrome in a Ghanaian child: a case report.
Badoe EV
West Afr J Med; 2009 Mar; 28(2):134-6. PubMed ID: 19761180
[TBL] [Abstract][Full Text] [Related]
19. Rett syndrome symptomatology of institutionalized adults with mental retardation: comparison of males and females.
Burd L; Randall T; Martsolf JT; Kerbeshian J
Am J Ment Retard; 1991 Mar; 95(5):596-601. PubMed ID: 2043352
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]