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 *

133 related articles for article (PubMed ID: 8985533)

  • 21. Rett syndrome.
    Chew CT; Lyen KR
    J Singapore Paediatr Soc; 1989; 31(1-2):82-9. PubMed ID: 2475669
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Rett syndrome. The Puerto Rican experience.
    Rivera Reyes L; Toro Solá MA
    Bol Asoc Med P R; 1990 Jun; 82(6):248-54. PubMed ID: 2222681
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [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]  

  • 24. Rett syndrome in Thai female girls: clinical studies.
    Phancharoen S
    J Med Assoc Thai; 2001 Jun; 84 Suppl 1():S57-60. PubMed ID: 11529381
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Therapeutic effects of a ketogenic diet in Rett syndrome.
    Haas RH; Rice MA; Trauner DA; Merritt TA
    Am J Med Genet Suppl; 1986; 1():225-46. PubMed ID: 3087185
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A Rett patient with a typical Angelman EEG.
    Laan LA; Vein AA
    Epilepsia; 2002 Dec; 43(12):1590-2. PubMed ID: 12460263
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Clinical phenotypes of classic Rett syndrome].
    Nieto-Barrera M; Nieto-Jiménez M; Siljeström ML
    Rev Neurol; 2003 Feb; 36 Suppl 1():S146-52. PubMed ID: 12599117
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. A novel STXBP1 mutation causes typical Rett syndrome in a Japanese girl.
    Yuge K; Iwama K; Yonee C; Matsufuji M; Sano N; Saikusa T; Yae Y; Yamashita Y; Mizuguchi T; Matsumoto N; Matsuishi T
    Brain Dev; 2018 Jun; 40(6):493-497. PubMed ID: 29544889
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Male Rett variant.
    Christen HJ; Hanefeld F
    Neuropediatrics; 1995 Apr; 26(2):81-2. PubMed ID: 7566459
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Rett syndrome: review of biological abnormalities.
    Dunn HG; MacLeod PM
    Can J Neurol Sci; 2001 Feb; 28(1):16-29. PubMed ID: 11252289
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Neurophysiology of Rett syndrome.
    Glaze DG
    Ment Retard Dev Disabil Res Rev; 2002; 8(2):66-71. PubMed ID: 12112729
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Early development and regression in Rett syndrome.
    Lee JY; Leonard H; Piek JP; Downs J
    Clin Genet; 2013 Dec; 84(6):572-6. PubMed ID: 23347273
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Rett syndrome--two case reports.
    Siew HF; Rani JM
    Med J Malaysia; 1991 Jun; 46(2):192-8. PubMed ID: 1839426
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Pons tumour behind a phenotypic Rett syndrome presentation.
    Vanhala R; Gaily E; Paetau A; Riikonen R
    Dev Med Child Neurol; 1998 Dec; 40(12):836-9. PubMed ID: 9881680
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Rett syndrome].
    Amarales L; Ortiz M
    Rev Chil Pediatr; 1989; 60(4):222-5. PubMed ID: 2485514
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Early stages of the Rett syndrome and infantile neuronal ceroid lipofuscinosis--a difficult differential diagnosis.
    Hagberg B; Witt-Engerström I
    Brain Dev; 1990; 12(1):20-2. PubMed ID: 2344018
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Rett syndrome: a case presenting with atypical seizures. Neurophysiological and clinical aspects.
    Pardal-Fernández JM; Jerez-García P; Onsurbe-Ramírez I; Marco-Giner J
    Neurophysiol Clin; 2004 Feb; 34(1):49-57. PubMed ID: 15030800
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.