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 *

94 related articles for article (PubMed ID: 10964075)

  • 1. Does a peculiar EEG pattern exist also for FRAXE mental retardation?
    Musumeci SA; Scuderi C; Ferri R; Anello G; Salluzzo R; Bosco P; Elia M
    Clin Neurophysiol; 2000 Sep; 111(9):1632-6. PubMed ID: 10964075
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The FMR2 gene, FRAXE and non-specific X-linked mental retardation: clinical and molecular aspects.
    Gecz J
    Ann Hum Genet; 2000 Mar; 64(Pt 2):95-106. PubMed ID: 11246464
    [TBL] [Abstract][Full Text] [Related]  

  • 3. FMR2 expression in families with FRAXE mental retardation.
    Gécz J; Oostra BA; Hockey A; Carbonell P; Turner G; Haan EA; Sutherland GR; Mulley JC
    Hum Mol Genet; 1997 Mar; 6(3):435-41. PubMed ID: 9147647
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of the gene FMR2, associated with FRAXE mental retardation.
    Gecz J; Gedeon AK; Sutherland GR; Mulley JC
    Nat Genet; 1996 May; 13(1):105-8. PubMed ID: 8673085
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lack of FMR3 expression in a male with non-syndromic mental retardation and a microdeletion immediately distal to FRAXE CCG repeat.
    Santos-Rebouças CB; Abdalla CB; Fullston T; Campos M; Pimentel MM; Gécz J
    Neurosci Lett; 2006 Apr; 397(3):245-8. PubMed ID: 16469443
    [TBL] [Abstract][Full Text] [Related]  

  • 6. FRAXE mutation in mentally retarded patients using the OxE18 probe.
    Mulatinho MV; Llerena JC; Pimentel MM
    Int J Mol Med; 2000 Jan; 5(1):67-9. PubMed ID: 10601577
    [TBL] [Abstract][Full Text] [Related]  

  • 7. FMR3 is a novel gene associated with FRAXE CpG island and transcriptionally silent in FRAXE full mutations.
    Gécz J
    J Med Genet; 2000 Oct; 37(10):782-4. PubMed ID: 11015457
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Instability of the FMR2 trinucleotide repeat region associated with expanded FMR1 alleles.
    Brown TC; Tarleton JC; Go RC; Longshore JW; Descartes M
    Am J Med Genet; 1997 Dec; 73(4):447-55. PubMed ID: 9415473
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [FRAXE mental retardation].
    Yamagata T
    Nihon Rinsho; 1999 Apr; 57(4):955-9. PubMed ID: 10222796
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Seizures and epileptiform EEG abnormalities in FRAXE syndrome.
    Musumeci SA; Ferri R; Scuderi C; Bosco P; Elia M
    Clin Neurophysiol; 2001 Oct; 112(10):1954-5. PubMed ID: 11601437
    [No Abstract]   [Full Text] [Related]  

  • 11. Localization of the fragile X mental retardation 2 (FMR2) protein in mammalian brain.
    Miller WJ; Skinner JA; Foss GS; Davies KE
    Eur J Neurosci; 2000 Jan; 12(1):381-4. PubMed ID: 10651894
    [TBL] [Abstract][Full Text] [Related]  

  • 12. FRAXE mutation in a mentally retarded subject and in his phenotypically normal twin brother.
    Lo Nigro C; Faravelli F; Cavani S; Perroni L; Novello P; Vitali M; Bricarelli FD; Grasso M
    Eur J Hum Genet; 2000 Mar; 8(3):157-62. PubMed ID: 10780779
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Bilateral centrotemporal spikes triggered by blinking: an unusual form of sensory input with related cortical EEG activity.
    Vetrugno R; Meletti S; Plazzi G; Posar A; Santucci M; Rossi PG; Lugaresi E; Liguori R
    Clin Neurophysiol; 1999 Nov; 110(11):1995-9. PubMed ID: 10576499
    [TBL] [Abstract][Full Text] [Related]  

  • 14. FMR2 function: insight from a mouse knockout model.
    Gu Y; Nelson DL
    Cytogenet Genome Res; 2003; 100(1-4):129-39. PubMed ID: 14526173
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Characterisation and expression of a large, 13.7 kb FMR2 isoform.
    Gecz J; Mulley JC
    Eur J Hum Genet; 1999; 7(2):157-62. PubMed ID: 10196698
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Screening for FMR1 and FMR2 mutations in 222 individuals from Spanish special schools: identification of a case of FRAXE-associated mental retardation.
    Milà M; Sànchez A; Badenas C; Brun C; Jiménez D; Villa MP; Castellví-Bel S; Estivill X
    Hum Genet; 1997 Oct; 100(5-6):503-7. PubMed ID: 9341861
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The influence of expanded unmethylated alleles for FRAXA/FRAXE loci in the intellectual performance among Brazilian mentally impaired males.
    Barros Santos C; Gonçalves Pimentel MM
    Int J Mol Med; 2003 Sep; 12(3):385-9. PubMed ID: 12883656
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new PCR assay useful for screening of FRAXE/FMR2 mental impairment among males.
    Santos CB; Costa Lima MA; Pimentel MM
    Hum Mutat; 2001 Aug; 18(2):157-62. PubMed ID: 11462240
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cognitive, behavioral, and neuroanatomical assessment of two unrelated male children expressing FRAXE.
    Abrams MT; Doheny KF; Mazzocco MM; Knight SJ; Baumgardner TL; Freund LS; Davies KE; Reiss AL
    Am J Med Genet; 1997 Feb; 74(1):73-81. PubMed ID: 9034011
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Age-related changes of cortical excitability in subjects with sleep-enhanced centrotemporal spikes: a somatosensory evoked potential study.
    Ferri R; Del Gracco S; Elia M; Musumeci SA
    Clin Neurophysiol; 2000 Apr; 111(4):591-9. PubMed ID: 10727909
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.