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Volumn 47, Issue 4, 2013, Pages 613-615

Basilar artery aneurysm: A new finding in classic infantile pompe disease

Author keywords

[No Author keywords available]

Indexed keywords

RECOMBINANT GLUCAN 1,4 ALPHA GLUCOSIDASE;

EID: 84875615706     PISSN: 0148639X     EISSN: 10974598     Source Type: Journal    
DOI: 10.1002/mus.23659     Document Type: Letter
Times cited : (6)

References (7)
  • 1
    • 47049095911 scopus 로고    scopus 로고
    • Dilative arteriopathy and basilar artery dolichoectasia complicating late-onset Pompe disease
    • Laforet P, Petiot P, Nicolino M, Orlikowski D, Callaud C, Pelligrini N, et al. Dilative arteriopathy and basilar artery dolichoectasia complicating late-onset Pompe disease. Neurology 2008;70:2063-2066.
    • (2008) Neurology , vol.70 , pp. 2063-2066
    • Laforet, P.1    Petiot, P.2    Nicolino, M.3    Orlikowski, D.4    Callaud, C.5    Pelligrini, N.6
  • 3
    • 79952202659 scopus 로고    scopus 로고
    • Abnormalities of cerebral arteries are frequent in patients with late-onset Pompe disease
    • Sacconi S, Bocquet JD, Chanelet S, Tanant V, Salviati L, Desnuelle C. Abnormalities of cerebral arteries are frequent in patients with late-onset Pompe disease. J Neurol 2010;257:1730-1733.
    • (2010) J Neurol , vol.257 , pp. 1730-1733
    • Sacconi, S.1    Bocquet, J.D.2    Chanelet, S.3    Tanant, V.4    Salviati, L.5    Desnuelle, C.6
  • 4
    • 79960840965 scopus 로고    scopus 로고
    • Expanding the clinical spectrum of late-onset Pompe disease: dilated arteriopathy involving the thoracic aorta, a novel vascular phenotype uncovered
    • El-Gharbawy AH, Bhat G, Murillo JE, Thurberg BL, Kampmann C, Mengel KE, et al. Expanding the clinical spectrum of late-onset Pompe disease: dilated arteriopathy involving the thoracic aorta, a novel vascular phenotype uncovered. Mol Genet Metab 2011;103:362-366.
    • (2011) Mol Genet Metab , vol.103 , pp. 362-366
    • El-Gharbawy, A.H.1    Bhat, G.2    Murillo, J.E.3    Thurberg, B.L.4    Kampmann, C.5    Mengel, K.E.6
  • 5
    • 33751211826 scopus 로고    scopus 로고
    • Characterization of pre- and post-treatment pathology after enzyme replacement therapy for Pompe disease
    • Thurberg BL, Lynch Maloney C, Vaccaro C, Afonso K, Tsai AC, Bossen E, et al. Characterization of pre- and post-treatment pathology after enzyme replacement therapy for Pompe disease. Lab Invest 2006;86:1208-1220.
    • (2006) Lab Invest , vol.86 , pp. 1208-1220
    • Thurberg, B.L.1    Lynch Maloney, C.2    Vaccaro, C.3    Afonso, K.4    Tsai, A.C.5    Bossen, E.6
  • 6
    • 77950518316 scopus 로고    scopus 로고
    • Prognostic factors for the late onset Pompe disease with enzyme replacement therapy: from our experience of 4 cases including an autopsy case
    • Kobayashi H, Shimada Y, Ikegami M, Kawai T, Sakurai K, Urashima T, et al. Prognostic factors for the late onset Pompe disease with enzyme replacement therapy: from our experience of 4 cases including an autopsy case. Mol Genet Metab 2010;100:14-19.
    • (2010) Mol Genet Metab , vol.100 , pp. 14-19
    • Kobayashi, H.1    Shimada, Y.2    Ikegami, M.3    Kawai, T.4    Sakurai, K.5    Urashima, T.6
  • 7
    • 0023226402 scopus 로고
    • Alpha-glucosidase deficiency and basilar artery aneurysm: report of a sibship
    • Makos MM, McComb RD, Hart MN, Bennett DR. Alpha-glucosidase deficiency and basilar artery aneurysm: report of a sibship. Ann Neurol 1987;22:629-633.
    • (1987) Ann Neurol , vol.22 , pp. 629-633
    • Makos, M.M.1    McComb, R.D.2    Hart, M.N.3    Bennett, D.R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.