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Volumn 19, Issue 2, 1997, Pages 177-179

Spontaneous remission of juvenile chronic myelomonocytic leukemia in an infant with noonan syndrome

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHRONIC MYELOMONOCYTIC LEUKEMIA; FEMALE; HUMAN; INFANT; LETTER; NOONAN SYNDROME; PATHOLOGY; PATHOPHYSIOLOGY; TUMOR REGRESSION;

EID: 0031086478     PISSN: 01928562     EISSN: None     Source Type: Journal    
DOI: 10.1097/00043426-199703000-00019     Document Type: Letter
Times cited : (44)

References (11)
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  • 2
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    • A pilot study of isotretinoin in the treatment of juvenile chronic myelogenous leukemia.
    • Castleberry RP, Emanuel PD, Zuckerman KS, et al. A pilot study of isotretinoin in the treatment of juvenile chronic myelogenous leukemia. N Engl J Med 1994;331:1680-4.
    • (1994) N Engl J Med , vol.331 , pp. 1680-4
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  • 3
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    • Pediatric myelodysplasia: a study of 68 children and a new prognostic scoring system.
    • Passmore SJ, Hann IM, Stiller CA, et al. Pediatric myelodysplasia: a study of 68 children and a new prognostic scoring system. Blood 1995;85:1742-50.
    • (1995) Blood , vol.85 , pp. 1742-50
    • Passmore, S.J.1    Hann, I.M.2    Stiller, C.A.3
  • 4
    • 0026063878 scopus 로고
    • Selective hypersensitivity to granulocyte-macrophage colony-stimulating factor by juvenile chronic myeloid leukemia hematopoietic progenitors.
    • Emanuel PD, Bates LJ, Castleberry RP, et al. Selective hypersensitivity to granulocyte-macrophage colony-stimulating factor by juvenile chronic myeloid leukemia hematopoietic progenitors. Blood 1991;77:925-9.
    • (1991) Blood , vol.77 , pp. 925-9
    • Emanuel, P.D.1    Bates, L.J.2    Castleberry, R.P.3
  • 5
    • 0021833752 scopus 로고
    • Persistent Epstein-Barr virus infection associated with monosomy 7 or chromosome 3 abnormality in childhood myeloproliferative disorders.
    • Stollmann B, Fonatsch C, Havers W. Persistent Epstein-Barr virus infection associated with monosomy 7 or chromosome 3 abnormality in childhood myeloproliferative disorders. Br J Haematol 1985;60:183-96.
    • (1985) Br J Haematol , vol.60 , pp. 183-96
    • Stollmann, B.1    Fonatsch, C.2    Havers, W.3
  • 6
    • 0014337521 scopus 로고
    • Hypertelorism with Turner phenotype.
    • Noonan J. Hypertelorism with Turner phenotype. Am J Dis Child 1968;116:373-80.
    • (1968) Am J Dis Child , vol.116 , pp. 373-80
    • Noonan, J.1
  • 7
    • 0014339668 scopus 로고
    • Noonan syndrome: a case with elevated serum alkaline phosphatase levels and malignant Schwannoma of the left forearm.
    • Kaplan MS, Opitz JM, Gosset FR. Noonan syndrome: a case with elevated serum alkaline phosphatase levels and malignant Schwannoma of the left forearm. Am J Dis Child 1968;116:359-66.
    • (1968) Am J Dis Child , vol.116 , pp. 359-66
    • Kaplan, M.S.1    Opitz, J.M.2    Gosset, F.R.3
  • 8
    • 0020160760 scopus 로고
    • Sindrome de Noonan asociado a leucosis aguda linfoblastica.
    • Merino AH, Etxeandia IA, Borja MB, et al. Sindrome de Noonan asociado a leucosis aguda linfoblastica. An Esp Pediatr 1982;17:78-80.
    • (1982) An Esp Pediatr , vol.17 , pp. 78-80
    • Merino, A.H.1    Etxeandia, I.A.2    Borja, M.B.3
  • 9
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    • Acute lymphoblastic leukemia in Noonan syndrome: report of two cases.
    • Piompo M, Rosanda C, Pasino M, et al. Acute lymphoblastic leukemia in Noonan syndrome: report of two cases. Med Pediatr Oncol 1993;21:454-5.
    • (1993) Med Pediatr Oncol , vol.21 , pp. 454-5
    • Piompo, M.1    Rosanda, C.2    Pasino, M.3
  • 10
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    • Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?
    • Stern HJ, Saal HM, Lee JS, et al. Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome? J Med Genet 1992;29:184-7.
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    • Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders.
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    • Shannon, K.M.1    O'Connell, P.2    Martin, G.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.