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Pediatric Radiology
Volumn 32, Issue 12, 2002, Pages 875-878
Neuroimaging abnormalities in Gricelli's disease
Author keywords

Brain calcification; Griscelli's disease; Haemophagocytosis; Neuroimaging
Indexed keywords

CYCLOSPORIN; DEXAMETHASONE; ETOPOSIDE; METHOTREXATE;
EID: 0036882275     PISSN: 03010449     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00247-002-0752-1     Document Type: Article
Times cited : (8)
References (8)
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    • Griscelli, C.1    Durandy, A.2    Guy-Grand, D.3
  • 2
    • 0032310971 scopus 로고    scopus 로고
    • Griscelli disease presenting with hemophagocytosis and cerebral involvement
    • Yalman N, Sarper N, Ünal E, et al (1998) Griscelli disease presenting with hemophagocytosis and cerebral involvement. Turk J Immunol 3:87-91
    • (1998) Turk J. Immunol. , vol.3 , pp. 87-91
    • Yalman, N.1    Sarper, N.2    Ünal, E.3
  • 3
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    • Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome
    • Menasche G, Pastural E, Feldman J, et al (2000) Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome. Nat Genet 25:173-176
    • (2000) Nat. Genet. , vol.25 , pp. 173-176
    • Menasche, G.1    Pastural, E.2    Feldman, J.3
  • 4
    • 0027936943 scopus 로고
    • Familial erythrophagocytic lymphohistiocytosis: Neuroradiologic evaluation with pathologic correlation
    • Kollias SS, Ball WS Jr, Tzika AA, et al (1994) Familial erythrophagocytic lymphohistiocytosis: neuroradiologic evaluation with pathologic correlation. Radiology 192:743-754
    • (1994) Radiology , vol.192 , pp. 743-754
    • Kollias, S.S.1    Ball W.S., Jr.2    Tzika, A.A.3
  • 5
    • 0035092422 scopus 로고    scopus 로고
    • Spectrum of perforin gene mutations in familial lymphohistiocytosis
    • Ericson KG, Fadeel B, Nilsson-Ardnor S, et al (2001) Spectrum of perforin gene mutations in familial lymphohistiocytosis, Am J Hum Genet 68:590-597
    • (2001) Am. J. Hum. Genet. , vol.68 , pp. 590-597
    • Ericson, K.G.1    Fadeel, B.2    Nilsson-Ardnor, S.3
  • 6
    • 0026562129 scopus 로고
    • Partial albinism with immunodeficiency: A rare syndrome with prominent posterior fossa white matter changes
    • Brismar J, Harfi HA (1992) Partial albinism with immunodeficiency: a rare syndrome with prominent posterior fossa white matter changes. AJNR 13:387-393
    • (1992) AJNR , vol.13 , pp. 387-393
    • Brismar, J.1    Harfi, H.A.2
  • 7
    • 0030943203 scopus 로고    scopus 로고
    • Frequency and severity of central nervous system lesions in hemophagocytic lymhohistiocytosis
    • Haddad E, Sulis ML, Jabado N, et al (1997) Frequency and severity of central nervous system lesions in hemophagocytic lymhohistiocytosis. Blood 889:794-800
    • (1997) Blood , vol.889 , pp. 794-800
    • Haddad, E.1    Sulis, M.L.2    Jabado, N.3
  • 8
    • 0030782433 scopus 로고    scopus 로고
    • Neuropathologic findings and neurologic symptoms in twenty-three children with hemophagocytic lymphohistiocytosis
    • Henter JI, Nennesmo I (1997) Neuropathologic findings and neurologic symptoms in twenty-three children with hemophagocytic lymphohistiocytosis. J Pediatr 130:358-365
    • (1997) J. Pediatr. , vol.130 , pp. 358-365
    • Henter, J.I.1    Nennesmo, I.2

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.