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Volumn 2, Issue 2, 2010, Pages 70-76

Aging in fragile X syndrome

Author keywords

Aging; Fragile X syndrome; Medical problems; Movement disorder

Indexed keywords


EID: 77954954470     PISSN: 18661947     EISSN: 18661955     Source Type: Journal    
DOI: 10.1007/s11689-010-9047-2     Document Type: Article
Times cited : (54)

References (45)
  • 1
    • 2542507386 scopus 로고    scopus 로고
    • A study of the distributional characteristics of FMR1 transcript levels in 238 individuals
    • Allen EG, He W, Yadav-Shah M, Sherman SL. A study of the distributional characteristics of FMR1 transcript levels in 238 individuals. Hum Genet. 2004; 114: 439-47.
    • (2004) Hum Genet , vol.114 , pp. 439-447
    • Allen, E.G.1    He, W.2    Yadav-Shah, M.3    Sherman, S.L.4
  • 2
    • 0036827976 scopus 로고    scopus 로고
    • Epilepsy in fragile X syndrome
    • Berry-Kravis E. Epilepsy in fragile X syndrome. Dev Med Child Neurol. 2002; 44: 724-8.
    • (2002) Dev Med Child Neurol , vol.44 , pp. 724-728
    • Berry-Kravis, E.1
  • 4
    • 70349090492 scopus 로고    scopus 로고
    • Handwriting movement analyses for monitoring drug-induced motor side effects in schizophrenia patients treated with risperidone
    • Caligiuri MP, Teulings HL, Dean CE, Niculescu AB, Lohr J. Handwriting movement analyses for monitoring drug-induced motor side effects in schizophrenia patients treated with risperidone. Hum Mov Sci. 2009; 28: 633-42.
    • (2009) Hum Mov Sci , vol.28 , pp. 633-642
    • Caligiuri, M.P.1    Teulings, H.L.2    Dean, C.E.3    Niculescu, A.B.4    Lohr, J.5
  • 9
    • 55949126144 scopus 로고    scopus 로고
    • Trends in hypertension prevalence, awareness, treatment, and control rates in United States adults between 1988-1994 and 1999-2004
    • Cutler JA, Sorlie PD, Wolz M, Thom T, Fields LE, Roccella EJ. Trends in hypertension prevalence, awareness, treatment, and control rates in United States adults between 1988-1994 and 1999-2004. Hypertension. 2008; 52: 818-27.
    • (2008) Hypertension , vol.52 , pp. 818-827
    • Cutler, J.A.1    Sorlie, P.D.2    Wolz, M.3    Thom, T.4    Fields, L.E.5    Roccella, E.J.6
  • 11
    • 0025361014 scopus 로고
    • Amyotrophic lateral sclerosis in a patient with fragile X syndrome
    • Desai HB, Donat J, Shokeir MH, Munoz DG. Amyotrophic lateral sclerosis in a patient with fragile X syndrome. Neurology. 1990; 40: 378-80.
    • (1990) Neurology , vol.40 , pp. 378-380
    • Desai, H.B.1    Donat, J.2    Shokeir, M.H.3    Munoz, D.G.4
  • 12
    • 69249118680 scopus 로고    scopus 로고
    • Screening for expanded alleles of the FMR1 gene in blood spots from newborn males in a Spanish population
    • Fernandez-Carvajal I, Walichiewicz P, Xiaosen X, Pan R, Hagerman PJ, Tassone F. Screening for expanded alleles of the FMR1 gene in blood spots from newborn males in a Spanish population. J Mol Diagn. 2009; 11: 324-9.
    • (2009) J Mol Diagn , vol.11 , pp. 324-329
    • Fernandez-Carvajal, I.1    Walichiewicz, P.2    Xiaosen, X.3    Pan, R.4    Hagerman, P.J.5    Tassone, F.6
  • 13
    • 77954952572 scopus 로고    scopus 로고
    • Greco C, Jin L-W, Tassone F, Hagerman P, Hagerman R. Neuropathological analysis of four fragile X syndrome (FXS) autopsy brains. 14th International Workshop on Fragile X Syndrome and X-linked mental retardation, Bahia, Brazil, 2009.
  • 14
    • 0001966753 scopus 로고    scopus 로고
    • Physical and behavioral phenotype
    • 3rd edn., R. J. Hagerman and P. J. Hagerman (Eds.), Baltimore: The Johns Hopkins University Press
    • Hagerman RJ. Physical and behavioral phenotype. In: Hagerman RJ, Hagerman PJ, editors. Fragile X syndrome: Diagnosis, treatment and research. 3rd ed. Baltimore: The Johns Hopkins University Press; 2002. p. 3-109.
    • (2002) Fragile X Syndrome: Diagnosis, Treatment and Research , pp. 3-109
    • Hagerman, R.J.1
  • 15
    • 76849083912 scopus 로고    scopus 로고
    • Origins of epilepsy in fragile X syndrome
    • Hagerman P, Stafstorm C. Origins of epilepsy in fragile X syndrome. Epilepsy Currents. 2009; 9: 108-12.
    • (2009) Epilepsy Currents , vol.9 , pp. 108-112
    • Hagerman, P.1    Stafstorm, C.2
  • 21
    • 77954952855 scopus 로고    scopus 로고
    • Hoeffer C, Klann E, Wong H, Hagerman R, Tassone F. Dysfunction of protein synthesis mediated by mTOR-dependent signaling in fragile x syndrome. 14th International Workshop on Fragile X Syndrome and X-linked mental retardation, Bahia, Brazil, 2009.
  • 22
    • 0034639857 scopus 로고    scopus 로고
    • Understanding the molecular basis of fragile X syndrome
    • Jin P, Warren ST. Understanding the molecular basis of fragile X syndrome. Hum Mol Genet. 2000; 9: 901-8.
    • (2000) Hum Mol Genet , vol.9 , pp. 901-908
    • Jin, P.1    Warren, S.T.2
  • 36
    • 0033955447 scopus 로고    scopus 로고
    • Pathological and neuropathological findings in two males with fragile-X syndrome
    • Sabaratnam M. Pathological and neuropathological findings in two males with fragile-X syndrome. J Intellect Disabil Res. 2000; 44(Pt 1): 81-5.
    • (2000) J Intellect Disabil Res , vol.44 , Issue.Pt 1 , pp. 81-85
    • Sabaratnam, M.1
  • 37
  • 38
    • 57749196405 scopus 로고    scopus 로고
    • Cancer incidence among persons with fragile X syndrome in Finland: A population-based study
    • Sund R, Pukkala E, Patja K. Cancer incidence among persons with fragile X syndrome in Finland: a population-based study. J Intellect Disabil Res. 2009; 53: 85-90.
    • (2009) J Intellect Disabil Res , vol.53 , pp. 85-90
    • Sund, R.1    Pukkala, E.2    Patja, K.3
  • 39
    • 0034684031 scopus 로고    scopus 로고
    • Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA
    • Tassone F, Hagerman RJ, Loesch DZ, Lachiewicz A, Taylor AK, Hagerman PJ. Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA. Am J Med Genet. 2000; 94: 232-6.
    • (2000) Am J Med Genet , vol.94 , pp. 232-236
    • Tassone, F.1    Hagerman, R.J.2    Loesch, D.Z.3    Lachiewicz, A.4    Taylor, A.K.5    Hagerman, P.J.6
  • 40
    • 0034945678 scopus 로고    scopus 로고
    • A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA
    • Tassone F, Hagerman RJ, Taylor AK, Hagerman PJ. A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA. J Med Genet. 2001; 38: 453-6.
    • (2001) J Med Genet , vol.38 , pp. 453-456
    • Tassone, F.1    Hagerman, R.J.2    Taylor, A.K.3    Hagerman, P.J.4
  • 41
    • 0023814453 scopus 로고
    • Aortic Hypoplasia and Cardiac Valvular Abnormalities in a Boy with Fragile-X Syndrome
    • Waldstein G, Hagerman R. Aortic Hypoplasia and Cardiac Valvular Abnormalities in a Boy with Fragile-X Syndrome. Am J Med Genet. 1988; 30: 83-98.
    • (1988) Am J Med Genet , vol.30 , pp. 83-98
    • Waldstein, G.1    Hagerman, R.2
  • 44
    • 33947195786 scopus 로고    scopus 로고
    • FMRP mediates mGluR5-dependent translation of amyloid precursor protein
    • Westmark CJ, Malter JS. FMRP mediates mGluR5-dependent translation of amyloid precursor protein. PLoS Biol. 2007; 5: e52.
    • (2007) PLoS Biol , vol.5
    • Westmark, C.J.1    Malter, J.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.