BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

374 related articles for article (PubMed ID: 25614013)

  • 1. Thyroid function in Rett syndrome.
    Stagi S; Cavalli L; Congiu L; Scusa MF; Ferlini A; Bigoni S; Benincasa A; Rossi B; Pini G
    Horm Res Paediatr; 2015; 83(2):118-25. PubMed ID: 25614013
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. [Thyroid hormone changes in women with pre-eclampsia and its relationship with the presence of pre-eclampsia].
    Zhou J; Du J; Ma B; Liu X; Qiu H; Li J; Wang X
    Zhonghua Fu Chan Ke Za Zhi; 2014 Feb; 49(2):109-13. PubMed ID: 24739642
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Immune dysfunction in Rett syndrome patients revealed by high levels of serum anti-N(Glc) IgM antibody fraction.
    Papini AM; Nuti F; Real-Fernandez F; Rossi G; Tiberi C; Sabatino G; Pandey S; Leoncini S; Signorini C; Pecorelli A; Guerranti R; Lavielle S; Ciccoli L; Rovero P; De Felice C; Hayek J
    J Immunol Res; 2014; 2014():260973. PubMed ID: 25389532
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Methyl-CpG-binding protein 2 gene and CDKL5 gene mutation in patients with Rett syndrome: analysis of 177 Chinese pediatric patients].
    Li MR; Pan H; Bao XH; Zhu XW; Cao GN; Zhang YZ; Wu XR
    Zhonghua Yi Xue Za Zhi; 2009 Feb; 89(4):224-9. PubMed ID: 19552836
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome.
    Mari F; Azimonti S; Bertani I; Bolognese F; Colombo E; Caselli R; Scala E; Longo I; Grosso S; Pescucci C; Ariani F; Hayek G; Balestri P; Bergo A; Badaracco G; Zappella M; Broccoli V; Renieri A; Kilstrup-Nielsen C; Landsberger N
    Hum Mol Genet; 2005 Jul; 14(14):1935-46. PubMed ID: 15917271
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Characterization of large deletions of the MECP2 gene in Rett syndrome patients by gene dosage analysis.
    Vidal S; Pascual-Alonso A; Rabaza-Gairí M; Gerotina E; Brandi N; Pacheco P; Xiol C; Pineda M; ; Armstrong J
    Mol Genet Genomic Med; 2019 Aug; 7(8):e793. PubMed ID: 31206249
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patients.
    Archer HL; Whatley SD; Evans JC; Ravine D; Huppke P; Kerr A; Bunyan D; Kerr B; Sweeney E; Davies SJ; Reardon W; Horn J; MacDermot KD; Smith RA; Magee A; Donaldson A; Crow Y; Hermon G; Miedzybrodzka Z; Cooper DN; Lazarou L; Butler R; Sampson J; Pilz DT; Laccone F; Clarke AJ
    J Med Genet; 2006 May; 43(5):451-6. PubMed ID: 16183801
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Early pospartum alexithymia and risk for depression: relationship with serum thyrotropin, free thyroid hormones and thyroid autoantibodies.
    Le Donne M; Settineri S; Benvenga S
    Psychoneuroendocrinology; 2012 Apr; 37(4):519-33. PubMed ID: 22047958
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Increases in thyrotropin within the near-normal range are associated with increased triiodothyronine but not increased thyroxine in the pediatric age group.
    Karavani G; Strich D; Edri S; Gillis D
    J Clin Endocrinol Metab; 2014 Aug; 99(8):E1471-5. PubMed ID: 24878053
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early pregnancy reference intervals of thyroid hormone concentrations in a thyroid antibody-negative pregnant population.
    Männistö T; Surcel HM; Ruokonen A; Vääräsmäki M; Pouta A; Bloigu A; Järvelin MR; Hartikainen AL; Suvanto E
    Thyroid; 2011 Mar; 21(3):291-8. PubMed ID: 21254924
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Assessment of thyroid function in two hundred patients with beta-thalassemia major.
    Zervas A; Katopodi A; Protonotariou A; Livadas S; Karagiorga M; Politis C; Tolis G
    Thyroid; 2002 Feb; 12(2):151-4. PubMed ID: 11916284
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. [Correlation between MECP2 genotype and phenotype in Chinese patients with Rett syndrome].
    Li MR; Pan H; Bao XH; Zhu XW; Cao GN; Zhang YZ; Wu XR
    Zhonghua Er Ke Za Zhi; 2009 Feb; 47(2):124-8. PubMed ID: 19573459
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Increased levels of 4HNE-protein plasma adducts in Rett syndrome.
    Pecorelli A; Ciccoli L; Signorini C; Leoncini S; Giardini A; D'Esposito M; Filosa S; Hayek J; De Felice C; Valacchi G
    Clin Biochem; 2011 Apr; 44(5-6):368-71. PubMed ID: 21276437
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.