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 *

172 related articles for article (PubMed ID: 15357687)

  • 41. The overlapping spectrum of rett and angelman syndromes: a clinical review.
    Jedele KB
    Semin Pediatr Neurol; 2007 Sep; 14(3):108-17. PubMed ID: 17980307
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Rett syndrome: prevalence among Chinese and a comparison of MECP2 mutations of classic Rett syndrome with other neurodevelopmental disorders.
    Wong VC; Li SY
    J Child Neurol; 2007 Dec; 22(12):1397-400. PubMed ID: 18174559
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Sympathetic overactivity and plasma leptin levels in Rett syndrome.
    Acampa M; Guideri F; Hayek J; Blardi P; De Lalla A; Zappella M; Auteri A
    Neurosci Lett; 2008 Feb; 432(1):69-72. PubMed ID: 18226448
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Stereotypical hand movements in 144 subjects with Rett syndrome from the population-based Australian database.
    Carter P; Downs J; Bebbington A; Williams S; Jacoby P; Kaufmann WE; Leonard H
    Mov Disord; 2010 Feb; 25(3):282-8. PubMed ID: 19908321
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Investigating the structure of the restricted, repetitive behaviours and interests domain of autism.
    Szatmari P; Georgiades S; Bryson S; Zwaigenbaum L; Roberts W; Mahoney W; Goldberg J; Tuff L
    J Child Psychol Psychiatry; 2006 Jun; 47(6):582-90. PubMed ID: 16712635
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Abnormal general movements in girls with Rett disorder: the first four months of life.
    Einspieler C; Kerr AM; Prechtl HF
    Brain Dev; 2005 Nov; 27 Suppl 1():S8-S13. PubMed ID: 16182501
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Rett syndrome from a family perspective: The Swedish Rett Center survey.
    Larsson G; Lindström B; Engerström IW
    Brain Dev; 2005 Nov; 27 Suppl 1():S14-S19. PubMed ID: 16182488
    [TBL] [Abstract][Full Text] [Related]  

  • 48. People with MECP2 mutation-positive Rett disorder who converse.
    Kerr AM; Archer HL; Evans JC; Prescott RJ; Gibbon F
    J Intellect Disabil Res; 2006 May; 50(Pt 5):386-94. PubMed ID: 16629931
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Motor stereotypies.
    Singer HS
    Semin Pediatr Neurol; 2009 Jun; 16(2):77-81. PubMed ID: 19501335
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Rett syndrome in South Africa.
    Moodley M
    Ann Trop Paediatr; 1992; 12(4):409-15. PubMed ID: 1283671
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Neurodevelopmental movement disorders - an update on childhood motor stereotypies.
    Barry S; Baird G; Lascelles K; Bunton P; Hedderly T
    Dev Med Child Neurol; 2011 Nov; 53(11):979-85. PubMed ID: 21749367
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Trihexyphenidyl for acute life-threatening episodes due to a dystonic movement disorder in Rett syndrome.
    Gika AD; Hughes E; Goyal S; Sparkes M; Lin JP
    Mov Disord; 2010 Feb; 25(3):385-9. PubMed ID: 20063434
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Rett syndrome: clinical and electrophysiologic aspects.
    Moser SJ; Weber P; Lütschg J
    Pediatr Neurol; 2007 Feb; 36(2):95-100. PubMed ID: 17275660
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Rett syndrome: of girls and mice--lessons for regression in autism.
    Glaze DG
    Ment Retard Dev Disabil Res Rev; 2004; 10(2):154-8. PubMed ID: 15362175
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Forensic issues and possible mechanisms of sudden death in Rett syndrome.
    Byard RW
    J Clin Forensic Med; 2006 Feb; 13(2):96-9. PubMed ID: 16263320
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Predictive value of the early clinical signs in Rett disorder.
    Kerr AM; Prescott RJ
    Brain Dev; 2005 Nov; 27 Suppl 1():S20-S24. PubMed ID: 16182500
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. Rett syndrome as a minicolumnopathy.
    Casanova MF; Buxhoeveden D; Switala A; Roy E
    Clin Neuropathol; 2003; 22(4):163-8. PubMed ID: 12908751
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Understanding, Recognizing, and Treating Rett Syndrome.
    Budden SS
    Medscape Womens Health; 1997 Mar; 2(3):3. PubMed ID: 9746685
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A functional assessment of handmouthing among persons with severe and profound intellectual disability.
    Swender SL; Matson JL; Mayville SB; Gonzalez ML; McDowell D
    J Intellect Dev Disabil; 2006 Jun; 31(2):95-100. PubMed ID: 16782594
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.