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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

162 related articles for article (PubMed ID: 21530498)

  • 1. F₄-neuroprostanes mediate neurological severity in Rett syndrome.
    Signorini C; De Felice C; Leoncini S; Giardini A; D'Esposito M; Filosa S; Della Ragione F; Rossi M; Pecorelli A; Valacchi G; Ciccoli L; Hayek J
    Clin Chim Acta; 2011 Jul; 412(15-16):1399-406. PubMed ID: 21530498
    [TBL] [Abstract][Full Text] [Related]  

  • 2. F(2)-Dihomo-isoprostanes and brain white matter damage in stage 1 Rett syndrome.
    Durand T; De Felice C; Signorini C; Oger C; Bultel-Poncé V; Guy A; Galano JM; Leoncini S; Ciccoli L; Pecorelli A; Valacchi G; Hayek J
    Biochimie; 2013 Jan; 95(1):86-90. PubMed ID: 23009927
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms.
    Fukuda T; Yamashita Y; Nagamitsu S; Miyamoto K; Jin JJ; Ohmori I; Ohtsuka Y; Kuwajima K; Endo S; Iwai T; Yamagata H; Tabara Y; Miki T; Matsuishi T; Kondo I
    Brain Dev; 2005 Apr; 27(3):211-7. PubMed ID: 15737703
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Altered erythrocyte membrane fatty acid profile in typical Rett syndrome: effects of omega-3 polyunsaturated fatty acid supplementation.
    Signorini C; De Felice C; Leoncini S; Durand T; Galano JM; Cortelazzo A; Zollo G; Guerranti R; Gonnelli S; Caffarelli C; Rossi M; Pecorelli A; Valacchi G; Ciccoli L; Hayek J
    Prostaglandins Leukot Essent Fatty Acids; 2014 Nov; 91(5):183-93. PubMed ID: 25240461
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Oxidative stress in Rett syndrome: natural history, genotype, and variants.
    Leoncini S; De Felice C; Signorini C; Pecorelli A; Durand T; Valacchi G; Ciccoli L; Hayek J
    Redox Rep; 2011; 16(4):145-53. PubMed ID: 21888765
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Cytokine Dysregulation in MECP2- and CDKL5-Related Rett Syndrome: Relationships with Aberrant Redox Homeostasis, Inflammation, and ω-3 PUFAs.
    Leoncini S; De Felice C; Signorini C; Zollo G; Cortelazzo A; Durand T; Galano JM; Guerranti R; Rossi M; Ciccoli L; Hayek J
    Oxid Med Cell Longev; 2015; 2015():421624. PubMed ID: 26236424
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Histone modifications in Rett syndrome lymphocytes: a preliminary evaluation.
    Kaufmann WE; Jarrar MH; Wang JS; Lee YJ; Reddy S; Bibat G; Naidu S
    Brain Dev; 2005 Aug; 27(5):331-9. PubMed ID: 16023547
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Effects of creatine supplementation in Rett syndrome: a randomized, placebo-controlled trial.
    Freilinger M; Dunkler D; Lanator I; Item CB; Mühl A; Fowler B; Bodamer OA
    J Dev Behav Pediatr; 2011; 32(6):454-60. PubMed ID: 21654506
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical profiles of four patients with Rett syndrome carrying a novel exon 1 mutation or genomic rearrangement in the MECP2 gene.
    Bartholdi D; Klein A; Weissert M; Koenig N; Baumer A; Boltshauser E; Schinzel A; Berger W; Mátyás G
    Clin Genet; 2006 Apr; 69(4):319-26. PubMed ID: 16630165
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Stereotypies in Rett syndrome: analysis of 83 patients with and without detected MECP2 mutations.
    Temudo T; Oliveira P; Santos M; Dias K; Vieira J; Moreira A; Calado E; Carrilho I; Oliveira G; Levy A; Barbot C; Fonseca M; Cabral A; Dias A; Cabral P; Monteiro J; Borges L; Gomes R; Barbosa C; Mira G; Eusébio F; Santos M; Sequeiros J; Maciel P
    Neurology; 2007 Apr; 68(15):1183-7. PubMed ID: 17420401
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Mutational analysis of MECP2 gene in Rett syndrome].
    Pan H; Wang Y; Meng H; Bao X; Zhang Y; Shen Y; Wu X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Aug; 19(4):276-80. PubMed ID: 12170461
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rett syndrome with and without detected MECP2 mutations: an attempt to redefine phenotypes.
    Temudo T; Santos M; Ramos E; Dias K; Vieira JP; Moreira A; Calado E; Carrilho I; Oliveira G; Levy A; Barbot C; Fonseca M; Cabral A; Cabral P; Monteiro J; Borges L; Gomes R; Mira G; Pereira SA; Santos M; Fernandes A; Epplen JT; Sequeiros J; Maciel P
    Brain Dev; 2011 Jan; 33(1):69-76. PubMed ID: 20116947
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Patients with Rett syndrome sustain low-energy fractures.
    Roende G; Ravn K; Fuglsang K; Andersen H; Vestergaard A; Brøndum-Nielsen K; Jensen JE; Nielsen JB
    Pediatr Res; 2011 Apr; 69(4):359-64. PubMed ID: 21178819
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Systemic oxidative stress in classic Rett syndrome.
    De Felice C; Ciccoli L; Leoncini S; Signorini C; Rossi M; Vannuccini L; Guazzi G; Latini G; Comporti M; Valacchi G; Hayek J
    Free Radic Biol Med; 2009 Aug; 47(4):440-8. PubMed ID: 19464363
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular update.
    Philippe C; Villard L; De Roux N; Raynaud M; Bonnefond JP; Pasquier L; Lesca G; Mancini J; Jonveaux P; Moncla A; Chelly J; Bienvenu T
    Eur J Med Genet; 2006; 49(1):9-18. PubMed ID: 16473305
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.