BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

344 related articles for article (PubMed ID: 17216643)

  • 1. Rett syndrome: an overlooked diagnosis in women with stereotypic hand movements, psychomotor retardation, Parkinsonism, and dystonia?
    Roze E; Cochen V; Sangla S; Bienvenu T; Roubergue A; Leu-Semenescu S; Vidaihet M
    Mov Disord; 2007 Feb; 22(3):387-9. PubMed ID: 17216643
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. Rett syndrome: a case report.
    Yodnopaklow P
    J Med Assoc Thai; 1996 Mar; 79(3):194-9. PubMed ID: 8708502
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rett syndrome: case reports and review.
    McIntosh RP; Simatos D; Weston HJ; Stanley TV
    N Z Med J; 1990 Mar; 103(886):122-5. PubMed ID: 2181354
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hand stereotypies distinguish Rett syndrome from autism disorder.
    Goldman S; Temudo T
    Mov Disord; 2012 Jul; 27(8):1060-2. PubMed ID: 22711266
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Rett's syndrome: report of 5 cases in Tunisia].
    Triki C; Mhiri C
    Rev Neurol (Paris); 1999 Nov; 155(11):955-9. PubMed ID: 10603640
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Rett syndrome and associated movement disorders.
    FitzGerald PM; Jankovic J; Percy AK
    Mov Disord; 1990; 5(3):195-202. PubMed ID: 2388636
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Perspectives on hand function in girls and women with Rett syndrome.
    Downs J; Parkinson S; Ranelli S; Leonard H; Diener P; Lotan M
    Dev Neurorehabil; 2014 Jun; 17(3):210-7. PubMed ID: 23869872
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. Evolution of stereotypies in adolescents and women with Rett syndrome.
    Vignoli A; La Briola F; Canevini MP
    Mov Disord; 2009 Jul; 24(9):1379-83. PubMed ID: 19425070
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Rett syndrome. A well defined but mysterious encephalopathy].
    Arzimanoglou A
    Rev Prat; 1991 Sep; 41(20):1940-4. PubMed ID: 1925380
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An analogue assessment of repetitive hand behaviours in girls and young women with Rett syndrome.
    Wales L; Charman T; Mount RH
    J Intellect Disabil Res; 2004 Oct; 48(Pt 7):672-8. PubMed ID: 15357687
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. A case of Rett syndrome.
    Lazuardi S; Advani N; Ismael S
    Paediatr Indones; 1989; 29(11-12):241-4. PubMed ID: 2488241
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Myoclonic status misdiagnosed as movement disorders in Rett syndrome: a video-polygraphic study.
    d'Orsi G; Demaio V; Minervini MG
    Epilepsy Behav; 2009 Jun; 15(2):260-2. PubMed ID: 19336260
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Rett syndrome a developmental disorder. Presentation of a variant with preserved speech].
    Sørensen E; Viken B
    Tidsskr Nor Laegeforen; 1995 Feb; 115(5):588-90. PubMed ID: 7900110
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rett syndrome.
    Choong CT; Lyen KR
    J Singapore Paediatr Soc; 1990; 32(3-4):169-76. PubMed ID: 2133757
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. [Clinical study of four cases of Rett Syndrome].
    Conde López VJ; Ballesteros Alcalde MC; Franco Martín MA; Geijo Uribe MS
    Actas Luso Esp Neurol Psiquiatr Cienc Afines; 1995; 23(3):138-55. PubMed ID: 7645416
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.