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4. Rett syndrome in Sri Lanka. Harendra de Silva DG Ceylon Med J; 1988 Jun; 33(2):73-5. PubMed ID: 3240435 [No Abstract] [Full Text] [Related]
5. Rett syndrome: genetic clues based on mitochondrial changes in muscle. Eeg-Olofsson O; al-Zuhair AG; Teebi AS; al-Essa MM Am J Med Genet; 1989 Jan; 32(1):142-4. PubMed ID: 2705475 [No Abstract] [Full Text] [Related]
6. Infantile autism and Rett's syndrome: common chromosomal denominator. Gillberg C; Wahlström J; Hagberg B Lancet; 1984 Nov; 2(8411):1094-5. PubMed ID: 6150162 [No Abstract] [Full Text] [Related]
7. Genetic implications of Rett syndrome. Wahlström J Brain Dev; 1985; 7(6):573-4. PubMed ID: 3832947 [TBL] [Abstract][Full Text] [Related]
8. Rett syndrome: a survey of North American patients. Coleman M; Brubaker J; Hunter K; Smith G J Ment Defic Res; 1988 Apr; 32 ( Pt 2)():117-24. PubMed ID: 3398038 [TBL] [Abstract][Full Text] [Related]
10. A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases. Hagberg B; Aicardi J; Dias K; Ramos O Ann Neurol; 1983 Oct; 14(4):471-9. PubMed ID: 6638958 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Rett's syndrome: characterization of respiratory patterns and sleep. Glaze DG; Frost JD; Zoghbi HY; Percy AK Ann Neurol; 1987 Apr; 21(4):377-82. PubMed ID: 3579223 [TBL] [Abstract][Full Text] [Related]
14. The velocardiofacial syndrome in older age: dementia and autistic features. Evers LJ; Vermaak MP; Engelen JJ; Curfs LM Genet Couns; 2006; 17(3):333-40. PubMed ID: 17100202 [TBL] [Abstract][Full Text] [Related]
15. [Rett syndrome. Review of the literature and presentation of 2 clinical cases]. Galli V; Ciccarone V; Venuta A; Ferrari P; Cavazzuti GB Pediatr Med Chir; 1985; 7(1):23-7. PubMed ID: 4088913 [TBL] [Abstract][Full Text] [Related]
16. Mast syndrome: a recessively inherited form of presenile dementia with motor disturbances. Cross HE Birth Defects Orig Artic Ser; 1971 Feb; 7(1):214-5. PubMed ID: 5173363 [No Abstract] [Full Text] [Related]
17. Non-movement disorder heralds symptoms of Machado-Joseph disease years before ataxia. D'Abreu A; Friedman J; Coskun J Mov Disord; 2005 Jun; 20(6):739-41. PubMed ID: 15747372 [TBL] [Abstract][Full Text] [Related]
18. No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients. Vourc'h P; Bienvenu T; Beldjord C; Chelly J; Barthélémy C; Müh JP; Andres C Eur J Hum Genet; 2001 Jul; 9(7):556-8. PubMed ID: 11464249 [TBL] [Abstract][Full Text] [Related]
19. Atypical clinical course of FXTAS: rapidly progressive dementia as the major symptom. Gonçalves MR; Capelli LP; Nitrini R; Barbosa ER; Porto CS; Lucato LT; Vianna-Morgante AM Neurology; 2007 May; 68(21):1864-6. PubMed ID: 17515552 [No Abstract] [Full Text] [Related]
20. Movement disorders in Rett syndrome: an analysis of 60 patients with detected MECP2 mutation and correlation with mutation type. Temudo T; Ramos E; Dias K; Barbot C; Vieira JP; Moreira A; Calado E; Carrilho I; Oliveira G; Levy A; Fonseca M; Cabral A; Cabral P; Monteiro JP; Borges L; Gomes R; Santos M; Sequeiros J; Maciel P Mov Disord; 2008 Jul; 23(10):1384-90. PubMed ID: 18512755 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]