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 *

97 related articles for article (PubMed ID: 7566454)

  • 21. Trisomy 21 and Rett syndrome: a double burden.
    Leonard H; Weaving L; Eastaugh P; Smith L; Delatycki M; Witt Engerström I; Christodoulou J
    J Paediatr Child Health; 2004 Jul; 40(7):406-9. PubMed ID: 15228575
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The development of visual- and auditory processing in Rett syndrome: an ERP study.
    Stauder JE; Smeets EE; van Mil SG; Curfs LG
    Brain Dev; 2006 Sep; 28(8):487-94. PubMed ID: 16647236
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Rett's syndrome - a neurodevelopmental disorder: report of two cases.
    Malhotra S; Kumar D; Gupta N
    Neurol India; 2002 Sep; 50(3):330-3. PubMed ID: 12391464
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Early determinants of fractures in Rett syndrome.
    Downs J; Bebbington A; Woodhead H; Jacoby P; Jian L; Jefferson A; Leonard H
    Pediatrics; 2008 Mar; 121(3):540-6. PubMed ID: 18310203
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Rett's syndrome. Clinical features and advances in genetics].
    Temudo T; Maciel P
    Rev Neurol; 2002 Feb; 34 Suppl 1():S54-8. PubMed ID: 12447790
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Diagnostic criteria for Rett syndrome. The Rett Syndrome Diagnostic Criteria Work Group.
    Ann Neurol; 1988 Apr; 23(4):425-8. PubMed ID: 2454607
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Gross rearrangements in the MECP2 gene in three patients with Rett syndrome: implications for routine diagnosis of Rett syndrome.
    Schollen E; Smeets E; Deflem E; Fryns JP; Matthijs G
    Hum Mutat; 2003 Aug; 22(2):116-20. PubMed ID: 12872251
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The story of Rett syndrome: from clinic to neurobiology.
    Chahrour M; Zoghbi HY
    Neuron; 2007 Nov; 56(3):422-37. PubMed ID: 17988628
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype.
    Hoffbuhr KC; Moses LM; Jerdonek MA; Naidu S; Hoffman EP
    Ment Retard Dev Disabil Res Rev; 2002; 8(2):99-105. PubMed ID: 12112735
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Rett syndrome: a diagnostic, clinical and molecular update].
    Tejada MI
    Rev Neurol; 2006 Jan; 42 Suppl 1():S55-9. PubMed ID: 16506134
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Towards a full life with Rett disorder.
    Kerr AM; Burford B
    Pediatr Rehabil; 2001; 4(4):157-68; discussion 155-6. PubMed ID: 12160356
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome.
    Voutoufianakis S; Psoni S; Vorgia P; Tsekoura F; Kekou K; Traeger-Synodinos J; Kitsiou S; Kanavakis E; Fryssira H
    Eur J Paediatr Neurol; 2007 Jul; 11(4):235-9. PubMed ID: 17276711
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Age-related occurrence of signs and symptoms in the Rett syndrome.
    Witt Engerström I
    Brain Dev; 1992 May; 14 Suppl():S11-20. PubMed ID: 1378244
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Disorganized rhythm and synchrony: early signs of autism and Rett syndrome.
    Trevarthen C; Daniel S
    Brain Dev; 2005 Nov; 27 Suppl 1():S25-S34. PubMed ID: 16182487
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Alterations in dopaminergic function in Rett syndrome.
    Wenk GL
    Neuropediatrics; 1995 Apr; 26(2):123-5. PubMed ID: 7566450
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Preliminary evidence for neurodegenerative changes in the substantia nigra of Rett syndrome.
    Kitt CA; Wilcox BJ
    Neuropediatrics; 1995 Apr; 26(2):114-8. PubMed ID: 7566448
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Rett syndrome].
    Vardi G; Galil A; Shorer Z; Porter B
    Harefuah; 1993 Jan; 124(2):78-81, 119. PubMed ID: 8436326
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Balanced X chromosome inactivation patterns in the Rett syndrome brain.
    Shahbazian MD; Sun Y; Zoghbi HY
    Am J Med Genet; 2002 Aug; 111(2):164-8. PubMed ID: 12210344
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Developmental profile of serum nerve growth factor levels in Rett complex.
    Calamandrei G; Aloe L; Hajek J; Zappella M
    Ann Ist Super Sanita; 2001; 37(4):601-5. PubMed ID: 12046231
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.