-
1
-
-
0021233189
-
Subacute and chronic myelomonocytic leukemia in children (juvenile CML).
-
Castro-Malaspina H, Schaison G, Passe S, et al. Subacute and chronic myelomonocytic leukemia in children (juvenile CML). Cancer 1984;54:675-86.
-
(1984)
Cancer
, vol.54
, pp. 675-86
-
-
Castro-Malaspina, H.1
Schaison, G.2
Passe, S.3
-
2
-
-
0028138595
-
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
-
-
Castleberry, R.P.1
Emanuel, P.D.2
Zuckerman, K.S.3
-
3
-
-
0028967873
-
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
-
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
-
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
-
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
-
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
-
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
-
-
0027198793
-
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
-
-
0026583146
-
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.
-
(1992)
J Med Genet
, vol.29
, pp. 184-7
-
-
Stern, H.J.1
Saal, H.M.2
Lee, J.S.3
-
11
-
-
0027979146
-
Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders.
-
Shannon KM, O'Connell P, Martin GA, et al. Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders. N Engl J Med 1994;330:597-601.
-
(1994)
N Engl J Med
, vol.330
, pp. 597-601
-
-
Shannon, K.M.1
O'Connell, P.2
Martin, G.A.3
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