Leukemic transformation in patients with severe congenital neutropenia

被引：8

作者：

Banerjee, A ^{[1
]}

Shannon, KM ^{[1
]}

机构：

[1] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA

来源：

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY | 2001年 / 23卷 / 08期

关键词：

D O I：

10.1097/00043426-200111000-00005

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

[No abstract available]

引用

页码：487 / 495

页数：9

共 58 条

[41]

MEMPEL K, 1991, BLOOD, V77, P1919

[42] CHILDHOOD CANCER AND CONGENITAL DEFECTS A STUDY OF US DEATH CERTIFICATES DURING PERIOD 1960-1966 [J].

MILLER, RW .

PEDIATRIC RESEARCH, 1969, 3 (05) :389-+

[43]

MIYAUCHI J, 1994, BLOOD, V83, P2248

[44] CORRECTION OF INFANTILE AGRANULOCYTOSIS (KOSTMANNS SYNDROME) BY ALLOGENIC BONE-MARROW TRANSPLANTATION [J].

RAPPEPORT, JM ;

PARKMAN, R ;

NEWBURGER, P ;

CAMITTA, BM ;

CHUSID, MJ .

AMERICAN JOURNAL OF MEDICINE, 1980, 68 (04) :605-609

[45]

Rodenhuis S, 1992, Semin Cancer Biol, V3, P241

[46] CONGENITAL AGRANULOCYTOSIS TERMINATING IN ACUTE MYELOMONOCYTIC LEUKEMIA [J].

ROSEN, RB ;

KANG, SJ .

JOURNAL OF PEDIATRICS, 1979, 94 (03) :406-408

[47] FAMILIAL BONE-MARROW MONOSOMY-7 - EVIDENCE THAT THE PREDISPOSING LOCUS IS NOT ON THE LONG ARM OF CHROMOSOME-7 [J].

SHANNON, KM ;

TURHAN, AG ;

CHANG, SSY ;

BOWCOCK, AM ;

ROGERS, PCJ ;

CARROLL, WL ;

COWAN, MJ ;

GLADER, BE ;

EAVES, CJ ;

EAVES, AC ;

KAN, YW .

JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (03) :984-989

[48] EVIDENCE IMPLICATING HETEROZYGOUS DELETION OF CHROMOSOME-7 IN THE PATHOGENESIS OF FAMILIAL LEUKEMIA ASSOCIATED WITH MONOSOMY-7 [J].

SHANNON, KM ;

TURHAN, AG ;

ROGERS, PCJ ;

KAN, YW .

GENOMICS, 1992, 14 (01) :121-125

[49] Clinical relevance of point mutations in the cytoplasmic domain of the granulocyte colony-stimulating factor receptor gene in patients with severe congenital neutropenia [J].

Tidow, N ;

Pilz, C ;

Teichmann, B ;

MullerBrechlin, A ;

Germeshausen, M ;

Kasper, B ;

Rauprich, P ;

Sykora, KW ;

Welte, K .

BLOOD, 1997, 89 (07) :2369-2375

[50] Defective internalization and sustained activation of truncated granulocyte colony-stimulating factor receptor found in severe congenital neutropenia/acute myeloid leukemia [J].

Ward, AC ;

van Aesch, YM ;

Schelen, AM ;

Touw, IP .

BLOOD, 1999, 93 (02) :447-458

← 1 2 3 4 5 6 →