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 *

120 related articles for article (PubMed ID: 10643242)

  • 1. [Rett syndrome--an odd handicap affecting girls. A current 25-year follow-up in Western Sweden].
    Hagberg B; Berg M; Steffenburg U
    Lakartidningen; 1999 Dec; 96(49):5488-90. PubMed ID: 10643242
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rett syndrome in Sweden. Neurodevelopment--disability--pathophysiology.
    Engerström IW
    Acta Paediatr Scand Suppl; 1990; 369():1-60. PubMed ID: 1701067
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Survival with Rett syndrome: comparing Rett's original sample with data from the Australian Rett Syndrome Database.
    Freilinger M; Bebbington A; Lanator I; De Klerk N; Dunkler D; Seidl R; Leonard H; Ronen GM
    Dev Med Child Neurol; 2010 Oct; 52(10):962-5. PubMed ID: 20573179
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. [Clinical and molecular genetic findings in four girls with Rett syndrome].
    Deutscher K; Deutscher J; Bergmann L; Tefs K; Reichwald K; Schuster V
    Klin Padiatr; 2002; 214(5):291-4. PubMed ID: 12235545
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. [Rett syndrome as a hodogenesis disorder].
    Narbona J
    Rev Neurol; 1999 Jan 1-15; 28(1):97-101. PubMed ID: 10101775
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Rett syndrome: clinical and molecular aspects].
    Záhoráková D; Zeman J; Martásek P
    Cas Lek Cesk; 2007; 146(8):647-52. PubMed ID: 17874730
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Three decades of sociomedical experiences from West Swedish Rett females 4-60 years of age.
    Hagberg B; Berg M; Steffenburg U
    Brain Dev; 2001 Dec; 23 Suppl 1():S28-31. PubMed ID: 11738838
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [Analysis of the most frequent mutations in girls with Rett syndrome].
    Rosipal R; Zeman J; Hadac J; Misovicová N; Nevsímalová S; Martásek P
    Cas Lek Cesk; 2001 Aug; 140(15):473-6. PubMed ID: 11569169
    [TBL] [Abstract][Full Text] [Related]  

  • 13. MECP2 mutations in Serbian Rett syndrome patients.
    Djarmati A; Dobricić V; Kecmanović M; Marsh P; Jancić-Stefanović J; Klein C; Djurić M; Romac S
    Acta Neurol Scand; 2007 Dec; 116(6):413-9. PubMed ID: 17986102
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Classical Rett Syndrome in a Ghanaian child: a case report.
    Badoe EV
    West Afr J Med; 2009 Mar; 28(2):134-6. PubMed ID: 19761180
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Rett females: patterns of characteristic side-asymmetric neuroimpairments at long-term follow-up.
    Hagberg B; Romell M
    Neuropediatrics; 2002 Dec; 33(6):324-6. PubMed ID: 12571789
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rett syndrome: a prototypical neurodevelopmental disorder.
    Neul JL; Zoghbi HY
    Neuroscientist; 2004 Apr; 10(2):118-28. PubMed ID: 15070486
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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]  

  • 18. Epidemiology of Rett syndrome: a population-based registry.
    Kozinetz CA; Skender ML; MacNaughton N; Almes MJ; Schultz RJ; Percy AK; Glaze DG
    Pediatrics; 1993 Feb; 91(2):445-50. PubMed ID: 8424025
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Rett syndrome: a search for gene sources.
    Akesson HO; Hagberg B; Wahlström J; Engerström IW
    Am J Med Genet; 1992 Jan; 42(1):104-8. PubMed ID: 1308347
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.