90 related articles for article (PubMed ID: 8538036)
1. [Hereditary hematopoietic malignancy with emphasis of juvenile chronic myelogenous leukemia and 7 monosomy syndrome].
Hayashi Y
Nihon Rinsho; 1995 Nov; 53(11):2737-41. PubMed ID: 8538036
[TBL] [Abstract][Full Text] [Related]
2. Chromosome pattern in juvenile chronic myelogenous leukemia, myelodysplastic syndrome, and acute leukemia associated with neurofibromatosis.
Kaneko Y; Maseki N; Sakurai M; Shibuya A; Shinohara T; Fujimoto T; Kanno H; Nishikawa A
Leukemia; 1989 Jan; 3(1):36-41. PubMed ID: 2491896
[TBL] [Abstract][Full Text] [Related]
3. Monosomy 7 myeloproliferative disease in children with neurofibromatosis, type 1: epidemiology and molecular analysis.
Shannon KM; Watterson J; Johnson P; O'Connell P; Lange B; Shah N; Steinherz P; Kan YW; Priest JR
Blood; 1992 Mar; 79(5):1311-8. PubMed ID: 1536955
[TBL] [Abstract][Full Text] [Related]
4. 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; Paderanga D; Olson K; Dinndorf P; McCormick F
N Engl J Med; 1994 Mar; 330(9):597-601. PubMed ID: 8302341
[TBL] [Abstract][Full Text] [Related]
5. Juvenile xanthogranuloma, neurofibromatosis, and juvenile chronic myelogenous leukemia. World statistical analysis.
Zvulunov A; Barak Y; Metzker A
Arch Dermatol; 1995 Aug; 131(8):904-8. PubMed ID: 7632061
[TBL] [Abstract][Full Text] [Related]
6. Monosomy 7 myeloproliferative disease associated with neurofibromatosis type I: a case report.
Savasan S; Zülfikar B; Ozgeneci A; Ozbek U; Sengün Z
J Chemother; 1996 Jun; 8(3):243-6. PubMed ID: 8808725
[TBL] [Abstract][Full Text] [Related]
7. Monosomy 7 myelodysplastic syndrome and other second malignant neoplasms in children with neurofibromatosis type 1.
Maris JM; Wiersma SR; Mahgoub N; Thompson P; Geyer RJ; Hurwitz CG; Lange BJ; Shannon KM
Cancer; 1997 Apr; 79(7):1438-46. PubMed ID: 9083167
[TBL] [Abstract][Full Text] [Related]
8. Myelodysplastic syndromes: the pediatric point of view.
Locatelli F; Zecca M; Pession A; Maserati E; De Stefano P; Severi F
Haematologica; 1995; 80(3):268-79. PubMed ID: 7672722
[TBL] [Abstract][Full Text] [Related]
9. Childhood myeloproliferative disorders.
Cotter FE
Baillieres Clin Haematol; 1998 Dec; 11(4):875-98. PubMed ID: 10640222
[TBL] [Abstract][Full Text] [Related]
10. p53 mutation as the second event in juvenile chronic myelogenous leukemia in a patient with neurofibromatosis type 1.
Luria D; Avigad S; Cohen IJ; Stark B; Weitz R; Zaizov R
Cancer; 1997 Nov; 80(10):2013-8. PubMed ID: 9366306
[TBL] [Abstract][Full Text] [Related]
11. Molecular evidence that childhood monosomy 7 syndrome is distinct from juvenile chronic myelogenous leukemia and other childhood myeloproliferative disorders.
Butcher M; Frenck R; Emperor J; Paderanga D; Maybee D; Olson K; Shannon K
Genes Chromosomes Cancer; 1995 Jan; 12(1):50-7. PubMed ID: 7534111
[TBL] [Abstract][Full Text] [Related]
12. A chronic myeloid leukemia-like syndrome case with del (12) (p12) in a Li-Fraumeni syndrome family.
Guran S; Beyan C; Nevruz O; Yakicier C; Tunca Y
Clin Lab Haematol; 2005 Apr; 27(2):135-8. PubMed ID: 15784129
[TBL] [Abstract][Full Text] [Related]
13. Loss of heterozygosity of NF1 gene in juvenile chronic myelogenous leukemia with neurofibromatosis type 1.
Kai S; Sumita H; Fujioka K; Takahashi H; Hanzawa N; Funabiki T; Ikuta K; Sasaki H
Int J Hematol; 1998 Jul; 68(1):53-60. PubMed ID: 9713168
[TBL] [Abstract][Full Text] [Related]
14. Juvenile chronic myelogenous leukemia, neurofibromatosis 1, and xanthoma.
Jang KA; Choi JH; Sung KJ; Moon KC; Koh JK; Im DJ
J Dermatol; 1999 Jan; 26(1):33-5. PubMed ID: 10063210
[TBL] [Abstract][Full Text] [Related]
15. Monosomy 7 syndrome in an infant with neurofibromatosis.
Kelleher JF; Carbone TV
Am J Pediatr Hematol Oncol; 1991; 13(3):338-41. PubMed ID: 1793161
[TBL] [Abstract][Full Text] [Related]
16. Skin, blood, nerve cells, and heritability. New lessons from neurofibromatosis type 1.
Riccardi VM
Arch Dermatol; 1995 Aug; 131(8):944. PubMed ID: 7632067
[No Abstract] [Full Text] [Related]
17. [Detection of trisomy 8 and monosomy 7 in chronic granulocytic leukemia and myelodysplastic syndrome by cytogenetic analysis and fluorescence in situ hybridization].
Szabó Gabriella P; Balogh E; Jakab Z; Germán P; Bodnár F; Kiss A; Telek B; Oláh E
Orv Hetil; 2002 Dec; 143(50):2775-9. PubMed ID: 12583317
[TBL] [Abstract][Full Text] [Related]
18. Monosomy 7 with severe myelodysplasia developing during imatinib treatment of Philadelphia-positive chronic myeloid leukemia: two cases with a different outcome.
Navarro JT; Feliu E; Grau J; Espinet B; Colomer D; Ribera JM; Oriol A; Granada I; Juncà J; Millá F
Am J Hematol; 2007 Sep; 82(9):849-51. PubMed ID: 17563075
[TBL] [Abstract][Full Text] [Related]
19. Mutations of the N-ras gene in juvenile chronic myelogenous leukemia.
Miyauchi J; Asada M; Sasaki M; Tsunematsu Y; Kojima S; Mizutani S
Blood; 1994 Apr; 83(8):2248-54. PubMed ID: 8161790
[TBL] [Abstract][Full Text] [Related]
20. Analysis of neurofibromatosis type 1 gene mutation in juvenile chronic myelogenous leukemia.
Watanabe I; Horiuchi T; Hatta N; Matsumoto M; Koike K; Kojima S; Ohga S; Fujita S
Acta Haematol; 1998; 100(1):22-5. PubMed ID: 9691142
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
