Li‐Fraumeni and Li‐Fraumeni—like syndrome among children diagnosed with pediatric cancer in Southern Brazil
暂无分享,去创建一个
P. Hainaut | P. Ashton-Prolla | C. Rossi | C. Netto | S. Camey | J. Goldim | M. Zagonel-Oliveira | J. Giacomazzi | Bárbara Alemar | A. Brunetto | S. Selistre | Patrícia Santos-Silva | G. Martel‐Planche | S.L. Cossio | D. Roth | F. S. Pereira | Marcelo Zagonel-Oliveira
[1] G. C. Piovezan. Prevalencia do alelo TP53 R337H no estado do Parana , 2013 .
[2] M. Fassnacht,et al. TP53 germline mutations in adult patients with adrenocortical carcinoma. , 2012, The Journal of clinical endocrinology and metabolism.
[3] M. Fassnacht,et al. Clinical impact of TP53 alterations in adrenocortical carcinomas , 2012, Langenbeck's Archives of Surgery.
[4] J. A. Yunes,et al. Association of the highly prevalent TP53 R337H mutation with pediatric choroid plexus carcinoma and osteosarcoma in Southeast Brazil , 2011, Cancer.
[5] E. Lalli,et al. Increased Incidence of Choroid Plexus Carcinoma Due to the Germline TP53 R337H Mutation in Southern Brazil , 2011, PloS one.
[6] P. Babyn,et al. Imaging of cancer predisposition syndromes in children. , 2011, Radiographics : a review publication of the Radiological Society of North America, Inc.
[7] M. Olivier,et al. Detailed haplotype analysis at the TP53 locus in p.R337H mutation carriers in the population of Southern Brazil: evidence for a founder effect , 2010, Human mutation.
[8] Catherine Bonaïti-Pellié,et al. 2009 version of the Chompret criteria for Li Fraumeni syndrome. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[9] S. Sommer,et al. Beyond Li Fraumeni Syndrome: clinical characteristics of families with p53 germline mutations. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[10] S. Shurtleff,et al. Association of the germline TP53 R337H mutation with breast cancer in southern Brazil , 2008, BMC Cancer.
[11] C. Bonaïti‐pellié,et al. Molecular basis of the Li–Fraumeni syndrome: an update from the French LFS families , 2008, Journal of Medical Genetics.
[12] M. Olivier,et al. Detection of R337H, a germline TP53 mutation predisposing to multiple cancers, in asymptomatic women participating in a breast cancer screening program in Southern Brazil. , 2008, Cancer letters.
[13] M. Olivier,et al. The TP53 mutation, R337H, is associated with Li-Fraumeni and Li-Fraumeni-like syndromes in Brazilian families. , 2007, Cancer letters.
[14] Andrew Shenton,et al. BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives. , 2006, European journal of cancer.
[15] P. Boffetta,et al. Penetrance of adrenocortical tumours associated with the germline TP53 R337H mutation , 2005, Journal of Medical Genetics.
[16] Charis Eng,et al. Highly penetrant hereditary cancer syndromes , 2004, Oncogene.
[17] D. Evans,et al. Low rate of TP53 germline mutations in breast cancer/sarcoma families not fulfilling classical criteria for Li-Fraumeni syndrome , 2002, Journal of medical genetics.
[18] E. Pinto,et al. An inherited mutation outside the highly conserved DNA-binding domain of the p53 tumor suppressor protein in children and adults with sporadic adrenocortical tumors. , 2001, The Journal of clinical endocrinology and metabolism.
[19] J. Varley,et al. Relative frequency and morphology of cancers in carriers of germline TP53 mutations , 2001, Oncogene.
[20] O. Delattre,et al. [Li-Fraumeni syndrome: update, new data and guidelines for clinical management]. , 2001, Bulletin du cancer.
[21] C. Bonaïti‐pellié,et al. Sensitivity and predictive value of criteria for p53germline mutation screening , 2001, Journal of medical genetics.
[22] C. Bonaïti‐pellié,et al. P53 germline mutations in childhood cancers and cancer risk for carrier individuals , 2000, British Journal of Cancer.
[23] D. Parkin,et al. Epidemiology of cancer: global patterns and trends. , 1998, Toxicology letters.
[24] J. Fraumeni,et al. Multiple primary cancers in families with Li-Fraumeni syndrome. , 1998, Journal of the National Cancer Institute.
[25] D. Evans,et al. Germ-line mutations of TP53 in Li-Fraumeni families: an extended study of 39 families. , 1997, Cancer research.
[26] A. Craft,et al. Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-Fraumeni families. , 1994, Cancer research.
[27] C. Marshall. Tumor suppressor genes , 1991, Cell.
[28] L. Strong,et al. Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. , 1990, Science.
[29] D. Parkin,et al. The international incidence of childhood cancer , 1988, IARC scientific publications.
[30] W. Blattner,et al. A cancer family syndrome in twenty-four kindreds. , 1988, Cancer research.
[31] J. Fraumeni,et al. Prospective study of a family cancer syndrome. , 1982, JAMA.
[32] Illinois.,et al. Cancer Genetics , 1976, British Journal of Cancer.
[33] J. Fraumeni,et al. Rhabdomyosarcoma in children: epidemiologic study and identification of a familial cancer syndrome. , 1969 .
[34] L. Strong. General keynote: hereditary cancer: lessons from Li-Fraumeni syndrome. , 2003, Gynecologic oncology.
[35] J. Varley. TP53, hChk2, and the Li-Fraumeni syndrome. , 2003, Methods in molecular biology.
[36] W. Mcdougal. An inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinoma. , 2002, The Journal of urology.
[37] Bruce A.J. Ponder,et al. Cancer genetics , 2001, Nature.
[38] R. Eeles. Germline mutations in the TP53 gene. , 1995, Cancer surveys.
[39] J. Higginson,et al. International Agency for Research on Cancer. , 1968, WHO chronicle.