Birth characteristics and the risk of childhood rhabdomyosarcoma based on histological subtype

[1]  S. Ognjanovic,et al.  Trends in childhood rhabdomyosarcoma incidence and survival in the United States, 1975‐2005 , 2009, Cancer.

[2]  Kimberly J. Johnson,et al.  Cancer Risk Among Children With Very Low Birth Weights , 2009, Pediatrics.

[3]  K. Michels,et al.  Birth weight and childhood leukemia: A meta‐analysis and review of the current evidence , 2009, International journal of cancer.

[4]  Erik B. Erhardt,et al.  Prenatal X-ray Exposure and Rhabdomyosarcoma in Children: A Report from the Children's Oncology Group , 2009, Cancer Epidemiology Biomarkers & Prevention.

[5]  Kimberly J. Johnson,et al.  Childhood Cancer among Twins and Higher Order Multiples , 2009, Cancer Epidemiology Biomarkers & Prevention.

[6]  Thomas Harder,et al.  Birth weight and subsequent risk of childhood primary brain tumors: a meta-analysis. , 2008, American journal of epidemiology.

[7]  N. de Klerk,et al.  Fetal growth and the risk of childhood non-CNS solid tumours in Western Australia , 2008, British Journal of Cancer.

[8]  A. Olshen,et al.  Global gene expression profiling of PAX‐FKHR fusion‐positive alveolar and PAX‐FKHR fusion‐negative embryonal rhabdomyosarcomas , 2007, The Journal of pathology.

[9]  M. Moschovi,et al.  Rhabdomyosarcoma in a patient with Noonan syndrome phenotype and review of the literature. , 2007, Journal of pediatric hematology/oncology.

[10]  A. Ferrari,et al.  Soft‐tissue sarcomas in children and adolescents with neurofibromatosis type 1 , 2007, Cancer.

[11]  R. Cohn,et al.  Recognition of Li Fraumeni syndrome at diagnosis of a locally advanced extremity rhabdomyosarcoma , 2007, Pediatric blood & cancer.

[12]  Silvia Behnke,et al.  Subtype and prognostic classification of rhabdomyosarcoma by immunohistochemistry. , 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[13]  Yukichi Tanaka,et al.  Germline mutations in HRAS proto-oncogene cause Costello syndrome , 2005, Nature Genetics.

[14]  K. Gripp.  Tumor predisposition in Costello syndrome , 2005, American journal of medical genetics. Part C, Seminars in medical genetics.

[15]  Eva Steliarova-Foucher,et al.  International Classification of Childhood Cancer, third edition , 2005, Cancer.

[16]  E. Forsum,et al.  Changes in basal metabolic rate during pregnancy in relation to changes in body weight and composition, cardiac output, insulin-like growth factor I, and thyroid hormones and in relation to fetal growth. , 2005, The American journal of clinical nutrition.

[17]  G. M. Taylor,et al.  Rhabdomyosarcoma in Nijmegen breakage syndrome: strong association with perianal primary site. , 2004, Cancer genetics and cytogenetics.

[18]  M. E. Calle,et al.  Risk factors for low birth weight: a review. , 2004, European journal of obstetrics, gynecology, and reproductive biology.

[19]  G. Sysyn,et al.  Abnormal fetal growth: intrauterine growth retardation, small for gestational age, large for gestational age. , 2004, Pediatric clinics of North America.

[20]  K. Joseph,et al.  Why are babies getting bigger? Temporal trends in fetal growth and its determinants. , 2002, The Journal of pediatrics.

[21]  M. Tekin,et al.  657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family , 2002, Clinical genetics.

[22]  M. Greaves.  Science, medicine, and the future: Childhood leukaemia , 2002 .

[23]  J. Michaelis,et al.  High birth weight and other risk factors for Wilms tumour: results of a population-based case-control study , 2001, European Journal of Pediatrics.

[24]  L. Helman,et al.  Rhabdomyosarcoma: an overview. , 1999, The oncologist.

[25]  M. Tucker,et al.  Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry. , 1998, The Journal of pediatrics.

[26]  E. Kramárová,et al.  The international classification of childhood cancer , 1996, International journal of cancer.

[27]  A. Gottlieb,et al.  Germline p53 mutations are frequently detected in young children with rhabdomyosarcoma. , 1995, The Journal of clinical investigation.

[28]  A. Schwartz,et al.  Parents' use of cocaine and marijuana and increased risk of rhabdomyosarcoma in their children , 1993, Cancer Causes & Control.

[29]  A. Feinberg,et al.  Relaxation of imprinted genes in human cancer , 1993, Nature.

[30]  K. Yoo,et al.  Association between childhood rhabdomyosarcoma and maternal history of stillbirths , 1992, International journal of cancer.

[31]  A. Fleming,et al.  Childhood leukaemia , 1991, The Lancet.

[32]  W. Cavenee,et al.  Molecular differential pathology of rhabdomyosarcoma , 1989, Genes, chromosomes & cancer.

[33]  J. Mann,et al.  The Inter-Regional Epidemiological Study of Childhood Cancer (IRESCC): case control study of children with bone and soft tissue sarcomas. , 1988, British Journal of Cancer.

[34]  J. Fraumeni,et al.  Rhabdomyosarcoma in children: epidemiologic study and identification of a familial cancer syndrome. , 1969, Journal of the National Cancer Institute.

[35]  J. Fraumeni,et al.  Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome? , 1969, Annals of internal medicine.

[36]  R. Arceci.  Identification of a PAX-FKHR Gene Expression Signature that Defines Molecular Classes and Determines the Prognosis of Alveolar Rhabdomyosarcomas , 2007 .

[37]  T. R. Knapp,et al.  The reliability and validity of birth certificates. , 2006, Journal of obstetric, gynecologic, and neonatal nursing : JOGNN.

[38]  N. Skakkebaek,et al.  A longitudinal study of intrauterine growth and the placental growth hormone (GH)-insulin-like growth factor I axis in maternal circulation: association between placental GH and fetal growth. , 2004, The Journal of clinical endocrinology and metabolism.

[39]  M. DeBaun,et al.  Hemihypertrophy and a poorly differentiated embryonal rhabdomyosarcoma of the pelvis. , 1999, Medical and pediatric oncology.

[40]  L. Ries,et al.  Cancer incidence and survival among children and adolescents: United States SEER Program 1975-1995. , 1999 .

[41]  E. Gehan,et al.  Congenital anomalies associated with rhabdomyosarcoma: an autopsy study of 115 cases. A report from the Intergroup Rhabdomyosarcoma Study Committee (representing the Children's Cancer Study Group, the Pediatric Oncology Group, the United Kingdom Children's Cancer Study Group, and the Pediatric Inter , 1988, Medical and pediatric oncology.

[42]  H. H. Wang,et al.  Environmental factors in the etiology of rhabdomyosarcoma in childhood. , 1982, Journal of the National Cancer Institute.