Armstrong J - Search Results

1

Cognitive stimulation has potential for brain activation in individuals with Rett syndrome.

Migliorelli C, Medina-Rivera I, Bachiller A, Tost A, Alonso JF, López-Sala A, Armstrong J, O'Callahan MDM, Pineda M, Mañanas MA, Romero S, García-Cazorla Á. Migliorelli C, et al. Among authors: armstrong j. J Intellect Disabil Res. 2022 Mar;66(3):213-224. doi: 10.1111/jir.12902. Epub 2021 Nov 18. J Intellect Disabil Res. 2022. PMID: 34796573

2

Mutation analysis of 16S rRNA in patients with Rett syndrome.

Armstrong J, Pineda M, Monrós E. Armstrong J, et al. Pediatr Neurol. 2000 Jul;23(1):85-7. doi: 10.1016/s0887-8994(00)00158-2. Pediatr Neurol. 2000. PMID: 10963979

3

Classic Rett syndrome in a boy as a result of somatic mosaicism for a MECP2 mutation.

Armstrong J, Pineda M, Aibar E, Geán E, Monrós E. Armstrong J, et al. Ann Neurol. 2001 Nov;50(5):692. doi: 10.1002/ana.1272. Ann Neurol. 2001. PMID: 11706982 No abstract available.

4

Rett syndrome in Spain: mutation analysis and clinical correlations.

Monrós E, Armstrong J, Aibar E, Poo P, Canós I, Pineda M. Monrós E, et al. Among authors: armstrong j. Brain Dev. 2001 Dec;23 Suppl 1:S251-3. doi: 10.1016/s0387-7604(01)00374-6. Brain Dev. 2001. PMID: 11738885

5

News and comment.

Armstrong J, Póo P, Pineda M, Aibar E, Geán E, Català V V, Monrós E. Armstrong J, et al. Ann Neurol. 2001 Nov;50(5):696. Ann Neurol. 2001. PMID: 11857656 No abstract available.

6

Prenatal diagnosis in Rett syndrome.

Armstrong J, Aibar E, Pineda M, Pérez MM, Geán E, Carrera M, Casas C, Martínez F, Monrós E. Armstrong J, et al. Fetal Diagn Ther. 2002 Jul-Aug;17(4):200-4. doi: 10.1159/000059370. Fetal Diagn Ther. 2002. PMID: 12065946

7

The impact of MECP2 mutations in the expression patterns of Rett syndrome patients.

Ballestar E, Ropero S, Alaminos M, Armstrong J, Setien F, Agrelo R, Fraga MF, Herranz M, Avila S, Pineda M, Monros E, Esteller M. Ballestar E, et al. Among authors: armstrong j. Hum Genet. 2005 Jan;116(1-2):91-104. doi: 10.1007/s00439-004-1200-0. Epub 2004 Nov 11. Hum Genet. 2005. PMID: 15549394

8

The X-linked methyl binding protein gene Kaiso is highly expressed in brain but is not mutated in Rett syndrome patients.

Della Ragione F, Tiunova A, Vacca M, Strazzullo M, González E, Armstrong J, Valero R, Campanile C, Pineda M, Hulten M, Monros E, D'Esposito M, Prokhortchouk E. Della Ragione F, et al. Among authors: armstrong j. Gene. 2006 May 24;373:83-9. doi: 10.1016/j.gene.2006.01.015. Epub 2006 Mar 13. Gene. 2006. PMID: 16530985

9

Novel FOXG1 mutations associated with the congenital variant of Rett syndrome.

Mencarelli MA, Spanhol-Rosseto A, Artuso R, Rondinella D, De Filippis R, Bahi-Buisson N, Nectoux J, Rubinsztajn R, Bienvenu T, Moncla A, Chabrol B, Villard L, Krumina Z, Armstrong J, Roche A, Pineda M, Gak E, Mari F, Ariani F, Renieri A. Mencarelli MA, et al. Among authors: armstrong j. J Med Genet. 2010 Jan;47(1):49-53. doi: 10.1136/jmg.2009.067884. Epub 2009 Jul 2. J Med Genet. 2010. PMID: 19578037

10

Abnormal expression of cerebrospinal fluid cation chloride cotransporters in patients with Rett syndrome.

Duarte ST, Armstrong J, Roche A, Ortez C, Pérez A, O'Callaghan Mdel M, Pereira A, Sanmartí F, Ormazábal A, Artuch R, Pineda M, García-Cazorla A. Duarte ST, et al. Among authors: armstrong j. PLoS One. 2013 Jul 19;8(7):e68851. doi: 10.1371/journal.pone.0068851. Print 2013. PLoS One. 2013. PMID: 23894354 Free PMC article.

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