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Volumn 150, Issue 3, 2004, Pages 611-613

Neurofibromatosis 1 associated with an intracranial artery abnormality, moyamoya disease and bilateral congenital large hairy pigmented macules [10]

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; CAROTID ARTERIOGRAPHY; CAROTID ARTERY OBSTRUCTION; CASE REPORT; CLINICAL EXAMINATION; DISEASE ASSOCIATION; FEMALE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; LETTER; MOYAMOYA DISEASE; NEUROFIBROMATOSIS; PIGMENT DISORDER; PRIORITY JOURNAL; SKIN BIOPSY;

EID: 1842506616     PISSN: 00070963     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2133.2004.05819.x     Document Type: Letter
Times cited : (8)

References (9)
  • 1
    • 0031016513 scopus 로고    scopus 로고
    • Somatic mosaicism for deletion of the entire NF1 gene identified by FISH
    • Wu BL, Boles RG, Yaari H et al. Somatic mosaicism for deletion of the entire NF1 gene identified by FISH. Hum Genet 1997; 99: 209-13.
    • (1997) Hum Genet , vol.99 , pp. 209-213
    • Wu, B.L.1    Boles, R.G.2    Yaari, H.3
  • 2
    • 0006954274 scopus 로고    scopus 로고
    • Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25
    • Yamauchi T, Tada M, Houkin K et al. Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25. Stroke 2000; 31: 930-5.
    • (2000) Stroke , vol.31 , pp. 930-935
    • Yamauchi, T.1    Tada, M.2    Houkin, K.3
  • 3
    • 0023885121 scopus 로고
    • Neurofibromatosis. Conference statement. National Institute of Health development conference
    • Stumpf DA, Alksne JF, Annergers JF et al. Neurofibromatosis. Conference statement. National Institute of Health development conference. Arch Neurol 1988; 45: 575-8.
    • (1988) Arch Neurol , vol.45 , pp. 575-578
    • Stumpf, D.A.1    Alksne, J.F.2    Annergers, J.F.3
  • 4
  • 5
    • 0023894373 scopus 로고
    • Cerebrovascular disorders associated with von Recklinghausen's neurofibromatosis: A case report
    • Sobata E, Ohmura H, Suzuki S. Cerebrovascular disorders associated with von Recklinghausen's neurofibromatosis: a case report. Neurosurgery 1988; 22: 544-9.
    • (1988) Neurosurgery , vol.22 , pp. 544-549
    • Sobata, E.1    Ohmura, H.2    Suzuki, S.3
  • 6
    • 0014477593 scopus 로고
    • Cerebrovascular 'moyamoya' disease
    • Suzuki J, Takaku A. Cerebrovascular 'moyamoya' disease. Arch Neurol 1969; 20: 288-99.
    • (1969) Arch Neurol , vol.20 , pp. 288-299
    • Suzuki, J.1    Takaku, A.2
  • 7
    • 0033118358 scopus 로고    scopus 로고
    • Non-anastomotic bypass surgery for childhood moyamoya disease using durai pedicle insertion over the brain surface combined with encephalogaleo-myosynangiosis
    • Yoshida YK, Shirane R, Yoshimoto T. Non-anastomotic bypass surgery for childhood moyamoya disease using durai pedicle insertion over the brain surface combined with encephalogaleo-myosynangiosis. Surg Neurol 1999; 51: 404-11.
    • (1999) Surg Neurol , vol.51 , pp. 404-411
    • Yoshida, Y.K.1    Shirane, R.2    Yoshimoto, T.3
  • 8
    • 0025326726 scopus 로고
    • A major segment of the neurofibromatosis 1 gene: cDNA sequence, genomic structure, and point mutation
    • Causon RM, Weiss R, Xu G et al. A major segment of the neurofibromatosis 1 gene: cDNA sequence, genomic structure, and point mutation. Cell 1990; 62: 193-201.
    • (1990) Cell , vol.62 , pp. 193-201
    • Causon, R.M.1    Weiss, R.2    Xu, G.3
  • 9
    • 0034961295 scopus 로고    scopus 로고
    • Large hairy pigmented spots in neurofibromatosis type 1: An atypical form of neurofibromas
    • Mahe E, Zeller J, Wolkenstein P et al. Large hairy pigmented spots in neurofibromatosis type 1: an atypical form of neurofibromas. Ann Dermatol Venereol 2001; 128: 619-21.
    • (2001) Ann Dermatol Venereol , vol.128 , pp. 619-621
    • Mahe, E.1    Zeller, J.2    Wolkenstein, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.