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Volumn 29, Issue 4, 2015, Pages 353-356

Early cerebellar hypometabolism in patients with frontotemporal dementia carrying the C9orf72 expansion

Author keywords

18F FDG PET; C9orf72; Frontotemporal dementia; Neuroimaging

Indexed keywords

APOLIPOPROTEIN E; FLUORODEOXYGLUCOSE F 18; LEVOTHYROXINE; PREDNISONE; C9ORF72 PROTEIN, HUMAN; PROTEIN; REPETITIVE DNA;

EID: 84947936776     PISSN: 08930341     EISSN: None     Source Type: Journal    
DOI: 10.1097/WAD.0000000000000056     Document Type: Article
Times cited : (7)

References (12)
  • 1
    • 80054832080 scopus 로고    scopus 로고
    • Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
    • DeJesus-Hernandez M, Mackenzie IR, Boeve BF, et al. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron. 2011;72:245-256.
    • (2011) Neuron. , vol.72 , pp. 245-256
    • DeJesus-Hernandez, M.1    Mackenzie, I.R.2    Boeve, B.F.3
  • 2
    • 80054837386 scopus 로고    scopus 로고
    • A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
    • Renton AE, Majounie E, Waite A, et al. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron. 2011;72:257-268.
    • (2011) Neuron. , vol.72 , pp. 257-268
    • Renton, A.E.1    Majounie, E.2    Waite, A.3
  • 3
    • 84863393788 scopus 로고    scopus 로고
    • Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72
    • Boeve BF, Boylan KB, Graff-Radford NR, et al. Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72. Brain. 2012;135:765-783.
    • (2012) Brain. , vol.135 , pp. 765-783
    • Boeve, B.F.1    Boylan, K.B.2    Graff-Radford, N.R.3
  • 4
    • 84866106544 scopus 로고    scopus 로고
    • Characterization of a family with c9FTD/ALS associated with the GGGGCC repeat expansion in C9ORF72
    • Savica R, Adeli A, Vemuri P, et al. Characterization of a family with c9FTD/ALS associated with the GGGGCC repeat expansion in C9ORF72. Arch Neurol. 2012;69:1164-1169.
    • (2012) Arch Neurol. , vol.69 , pp. 1164-1169
    • Savica, R.1    Adeli, A.2    Vemuri, P.3
  • 5
    • 84857588946 scopus 로고    scopus 로고
    • Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics
    • Whitwell JL, Weigand SD, Boeve BF, et al. Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics. Brain. 2012;135:794-806.
    • (2012) Brain. , vol.135 , pp. 794-806
    • Whitwell, J.L.1    Weigand, S.D.2    Boeve, B.F.3
  • 6
    • 84899124212 scopus 로고    scopus 로고
    • The metabolic signature of C9ORF72-related ALS: FDG PET comparison with nonmutated patients
    • Cistaro A, Pagani M, Montuschi A, et al. The metabolic signature of C9ORF72-related ALS: FDG PET comparison with nonmutated patients. Eur J Nucl Med Mol Imaging. 2014; 41:844-852.
    • (2014) Eur J Nucl Med Mol Imaging. , vol.41 , pp. 844-852
    • Cistaro, A.1    Pagani, M.2    Montuschi, A.3
  • 7
    • 84892451456 scopus 로고    scopus 로고
    • Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia
    • Dols-Icardo O, Garcia-Redondo A, Rojas-Garcia R, et al. Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia. Hum Mol Genet. 2014;3:749-754.
    • (2014) Hum Mol Genet. , vol.3 , pp. 749-754
    • Dols-Icardo, O.1    Garcia-Redondo, A.2    Rojas-Garcia, R.3
  • 8
    • 84861919479 scopus 로고    scopus 로고
    • Expansion mutation in C9ORF72 does not influence plasma progranulin levels in frontotemporal dementia
    • Dols-Icardo O, Suarez-Calvet M, Hernandez I, et al. Expansion mutation in C9ORF72 does not influence plasma progranulin levels in frontotemporal dementia. Neurobiol Aging. 2012;33: e17-e19.
    • (2012) Neurobiol Aging. , vol.33 , pp. e17-e19
    • Dols-Icardo, O.1    Suarez-Calvet, M.2    Hernandez, I.3
  • 9
    • 84896781404 scopus 로고    scopus 로고
    • Frontotemporal dementia associated with the C9ORF72 mutation: A unique clinical profile
    • Devenney E, Hornberger M, Irish M, et al. Frontotemporal dementia associated with the C9ORF72 mutation: a unique clinical profile. JAMA Neurol. 2014;71:331-339.
    • (2014) JAMA Neurol. , vol.71 , pp. 331-339
    • Devenney, E.1    Hornberger, M.2    Irish, M.3
  • 10
    • 0034107307 scopus 로고    scopus 로고
    • Diagnosis and monitoring of central nervous system involvement in systemic lupus erythematosus: Value of F-18 fluorodeoxyglucose PET
    • Weiner SM, Otte A, Schumacher M, et al. Diagnosis and monitoring of central nervous system involvement in systemic lupus erythematosus: value of F-18 fluorodeoxyglucose PET. Ann Rheum Dis. 2000;59:377-385.
    • (2000) Ann Rheum Dis. , vol.59 , pp. 377-385
    • Weiner, S.M.1    Otte, A.2    Schumacher, M.3
  • 11
    • 79953814616 scopus 로고    scopus 로고
    • Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p
    • Pearson JP, Williams NM, Majounie E, et al. Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p. J Neurol. 2011; 258:647-655.
    • (2011) J Neurol. , vol.258 , pp. 647-655
    • Pearson, J.P.1    Williams, N.M.2    Majounie, E.3
  • 12
    • 82355180826 scopus 로고    scopus 로고
    • P62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS
    • Al-Sarraj S, King A, Troakes C, et al. p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS. Acta Neuropathol. 2011;122:691-702.
    • (2011) Acta Neuropathol. , vol.122 , pp. 691-702
    • Al-Sarraj, S.1    King, A.2    Troakes, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.