메뉴 건너뛰기




Volumn 130, Issue 2, 1997, Pages 317-319

Prolonged extreme thrombocytosis associated with neurofibromatosis type 1

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; CAFE AU LAIT SPOT; CASE REPORT; CHROMOSOME 17Q; CLINICAL EXAMINATION; DISEASE ASSOCIATION; FEMALE; HUMAN; MEGAKARYOPOIESIS; NEUROFIBROMATOSIS; PRIORITY JOURNAL; THROMBOCYTE COUNT; THROMBOCYTHEMIA; THROMBOCYTOSIS;

EID: 0030678113     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(97)70363-9     Document Type: Article
Times cited : (6)

References (14)
  • 1
    • 0024307041 scopus 로고
    • Thrombocytosis in childhood: a survey of 94 patients
    • KW Chan Y Kaikov LD. Wadsworth Thrombocytosis in childhood: a survey of 94 patients Pediatrics 84 1989 1064 1067
    • (1989) Pediatrics , vol.84 , pp. 1064-1067
    • Chan, KW1    Kaikov, Y2    Wadsworth, LD.3
  • 3
    • 0018326112 scopus 로고
    • Thrombocytosis in low birthweight infants: a physiological phenomenon in infancy
    • U Lundström Thrombocytosis in low birthweight infants: a physiological phenomenon in infancy Arch Dis Child 54 1979 715 717
    • (1979) Arch Dis Child , vol.54 , pp. 715-717
    • Lundström, U1
  • 5
    • 0026319619 scopus 로고
    • cDNA cloning of the type 1 neurofibromatosis gene: complete sequence of the NF1 gene product
    • DA Marchuk AM Saulino R Tavakkol cDNA cloning of the type 1 neurofibromatosis gene: complete sequence of the NF1 gene product Genomics 11 1991 931 940
    • (1991) Genomics , vol.11 , pp. 931-940
    • Marchuk, DA1    Saulino, AM2    Tavakkol, R3
  • 6
    • 0027719341 scopus 로고
    • An incidental finding of extreme self-limited thrombocytosis of unknown cause
    • AW Cashell DH Buss CA. Johnson An incidental finding of extreme self-limited thrombocytosis of unknown cause WV Med J 89 1993 545 546
    • (1993) WV Med J , vol.89 , pp. 545-546
    • Cashell, AW1    Buss, DH2    Johnson, CA.3
  • 7
    • 0029164366 scopus 로고
    • Treatment of essential thrombocythemia with anagrelide
    • MM Chintagumpala LL Kennedy CP. Steuber Treatment of essential thrombocythemia with anagrelide J Pediatr 127 1995 495 498
    • (1995) J Pediatr , vol.127 , pp. 495-498
    • Chintagumpala, MM1    Kennedy, LL2    Steuber, CP.3
  • 8
    • 0028350733 scopus 로고
    • Occurrence, etiology, and clinical significance of extreme thrombocytosis: a study of 280 cases
    • DH Buss AW Cashell ML O'Connor F Richards LD. Case Occurrence, etiology, and clinical significance of extreme thrombocytosis: a study of 280 cases Am J Med 96 1994 247 253
    • (1994) Am J Med , vol.96 , pp. 247-253
    • Buss, DH1    Cashell, AW2    O'Connor, ML3    Richards, F4    Case, LD.5
  • 9
    • 0027974256 scopus 로고
    • Neurofibromatosis and childhood leukaemia/lymphoma: a population-based UKCCSG study
    • CA Stiller JM Chessells M. Fitchett Neurofibromatosis and childhood leukaemia/lymphoma: a population-based UKCCSG study Br J Cancer 70 1994 969 972
    • (1994) Br J Cancer , vol.70 , pp. 969-972
    • Stiller, CA1    Chessells, JM2    Fitchett, M.3
  • 10
    • 0029160129 scopus 로고
    • Childhood myelodysplastic syndrome in Denmark: incidence and predisposing conditions
    • H Hasle G Kerndrup BB. Jacobsen Childhood myelodysplastic syndrome in Denmark: incidence and predisposing conditions Leukemia 9 1995 1569 1572
    • (1995) Leukemia , vol.9 , pp. 1569-1572
    • Hasle, H1    Kerndrup, G2    Jacobsen, BB.3
  • 11
    • 0027979146 scopus 로고
    • Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders
    • KM Shannon P O'Connell GA Martin Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders N Engl J Med 330 1994 597 601
    • (1994) N Engl J Med , vol.330 , pp. 597-601
    • Shannon, KM1    O'Connell, P2    Martin, GA3
  • 12
    • 0027260737 scopus 로고
    • Absence of enhancement of spontaneous echocardiographic contrast by thrombocytosis in a patient with left ventricular aneurysm, primary thrombocythemia, and von Recklinghausen neurofibromatosis: a case report
    • JJ Monsuez M Janier AN Van Cao JR. Le Gall Absence of enhancement of spontaneous echocardiographic contrast by thrombocytosis in a patient with left ventricular aneurysm, primary thrombocythemia, and von Recklinghausen neurofibromatosis: a case report Angiology 44 1993 651 654
    • (1993) Angiology , vol.44 , pp. 651-654
    • Monsuez, JJ1    Janier, M2    Van Cao, AN3    Le Gall, JR.4
  • 13
    • 0028082464 scopus 로고
    • Deletions spanning the neurofibromatosis 1 gene: identification and phenotype of five patients
    • LM Kayes W Burke VM Riccardi Deletions spanning the neurofibromatosis 1 gene: identification and phenotype of five patients Am J Hum Genet 54 1994 424 436
    • (1994) Am J Hum Genet , vol.54 , pp. 424-436
    • Kayes, LM1    Burke, W2    Riccardi, VM3
  • 14
    • 0028799029 scopus 로고
    • Deletion of the entire NF1 gene detected by FISH: four deletion patients associated with severe manifestations
    • BL Wu MA Austin GH Schneider RG Boles BR. Korf Deletion of the entire NF1 gene detected by FISH: four deletion patients associated with severe manifestations Am J Med Genet 59 1995 528 535
    • (1995) Am J Med Genet , vol.59 , pp. 528-535
    • Wu, BL1    Austin, MA2    Schneider, GH3    Boles, RG4    Korf, BR.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.