Keyword Index

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Results 171 - 180 of 306 shown below

  • germ-cell tumour

    M J Fegg, A Gerl, T C Vollmer, U Gruber, C Jost, S Meiler and W Hiddemann

    Subjective quality of life and sexual functioning after germ-cell tumour therapy

    doi:10.1038/sj.bjc.6601421

  • A-C Piketty, A Fléchon, A Laplanche, E Nouyrigat, J-P Droz, C Théodore and K Fizazi

    The risk of thrombo-embolic events is increased in patients with germ-cell tumours and can be predicted by serum lactate dehydrogenase and body surface area

    advance online publication, 2005-10-04 00:00:00.000;

    doi:10.1038/sj.bjc.6602791

  • germ-cell tumours

    K Fizazi, D M Prow, K-A Do, X Wang, L Finn, J Kim, D Daliani, C N Papandreou, S-M Tu, R E Millikan, L C Pagliaro, C J Logothetis and R J Amato

    Alternating dose-dense chemotherapy in patients with high volume disseminated non-seminomatous germ cell tumours

    doi:10.1038/sj.bjc.6600272

  • German population

    C Maier, J Haeusler, K Herkommer, Z Vesovic, J Hoegel, W Vogel and T Paiss

    Mutation screening and association study of RNASEL as a prostate cancer susceptibility gene

    advance online publication, 2005-02-15 00:00:00.000;

    doi:10.1038/sj.bjc.6602401

  • Germany

    A Stang, C Stegmaier and K-H Jöckel

    Nonmelanoma skin cancer in the Federal State of Saarland, Germany, 1995–1999

    doi:10.1038/sj.bjc.6601294

  • J Schüz, U Kaletsch, R Meinert, P Kaatsch and J Michaelis

    Association of childhood leukaemia with factors related to the immune system

    doi:10.1038/sj.bjc.6690395

  • A Stang, C Stegmaier, B Eisinger, R Stabenow, K A Metz and K-H Jöckel

    Descriptive epidemiology of small intestinal malignancies: the German Cancer Registry experience

    doi:10.1038/sj.bjc.6690541

  • germinoma

    E Bouffet, M C Baranzelli, C Patte, M Portas, C Edan, P Chastagner, F Mechinaud-Lacroix and C Kalifa

    Combined treatment modality for intracranial germinomas: results of a multicentre SFOP experience

    doi:10.1038/sj.bjc.6690192

  • germline

    B G Davies, A Hussain, S M Ring, J M Birch, T O B Eden, M Reeves, Y E Dubrova and G M Taylor

    New germline mutations in the hypervariable minisatellite CEB1 in the parents of children with leukaemia

    advance online publication, 2007-03-27 00:00:00.000;

    doi:10.1038/sj.bjc.6603706

  • J Stone, S Bevan, D Cunningham, A Hill, N Rahman, J Peto, A Marossy and R S Houlston

    Low frequency of germline E-cadherin mutations in familial and nonfamilial gastric cancer

    doi:10.1038/sj.bjc.6690308

  • N Veldhoen, J Watterson, M Brash and J Milner

    Identification of tumour-associated and germ line p53 mutations in canine mammary cancer

    doi:10.1038/sj.bjc.6690709

  • N Rahman, J G Stone, G Coleman, B Gusterson, S Seal, A Marossy, S R Lakhani, A Ward, A Nash, A McKinna, R A'Hern, M R Stratton and R S Houlston

    Lobular carcinoma in situ of the breast is not caused by constitutional mutations in the E-cadherin gene

    doi:10.1054/bjoc.1999.0965

  • A Chompret, L Brugières, M Ronsin, M Gardes, F Dessarps-Freichey, A Abel, D Hua, L Ligot, M-G Dondon, B Bressac-de Paillerets, T Frébourg, J Lemerle, C Bonaïti-Pellié and J Feunteun

    P53 germline mutations in childhood cancers and cancer risk for carrier individuals

    doi:10.1054/bjoc.2000.1167

  • germline mutation

    N Soufir, J J Lacapere, G Bertrand, E Matichard, R Meziani, D Mirebeau, V Descamps, B Gérard, A Archimbaud, L Ollivaud, F Bouscarat, M Baccard, G Lanternier, P Saïag, C Lebbé, N Basset-Seguin, B Crickx, H Cave and B Grandchamp

    Germline mutations of the INK4a-ARF gene in patients with suspected genetic predisposition to melanoma

    doi:10.1038/sj.bjc.6601503

  • A C J Ammerlaan, A Ararou, M P W A Houben, F Baas, C C Tijssen, J L J M Teepen, P Wesseling and T J M Hulsebos

    Long-term survival and transmission of INI1-mutation via nonpenetrant males in a family with rhabdoid tumour predisposition syndrome

    advance online publication, 2007-12-18 00:00:00.000;

    doi:10.1038/sj.bjc.6604156

  • N Soufir, B Bressac-de Paillerets, L Desjardins, C Lévy, J Bombled, I Gorin, P Schlienger and D Stoppa-Lyonnet

    Individuals with presumably hereditary uveal melanoma do not harbour germline mutations in the coding regions of either the P16INK4A, P14ARF or cdk4 genes

    doi:10.1054/bjoc.1999.1005

  • K-A Yoon, J-L Ku, H S Choi, S C Heo, S-Y Jeong, Y J Park, N K Kim, J C Kim, P M Jung and J-G Park

    Germline mutations of the STK11 gene in Korean Peutz-Jeghers syndrome patients

    doi:10.1054/bjoc.1999.1125

  • germline mutations

    T Ohayon, R Gershoni-Baruch, M Z Papa, T Distelman Menachem, S Eisenberg Barzilai and E Friedman

    The R72P P53 mutation is associated with familial breast cancer in Jewish women

    advance online publication, 2005-03-01 00:00:00.000;

    doi:10.1038/sj.bjc.6602451

  • C Marian, A Scope, K Laud, E Friedman, F Pavlotsky, E Yakobson, B Bressac-de Paillerets and E Azizi

    Search for germline alterations in CDKN2A/ARF and CDK4 of 42 Jewish melanoma families with or without neural system tumours

    advance online publication, 2005-05-31 00:00:00.000;

    doi:10.1038/sj.bjc.6602629

  • C Pinto, I Veiga, M Pinheiro, B Mesquita, C Jeronimo, O Sousa, M Fragoso, L Santos, L Moreira-Dias, M Baptista, C Lopes, S Castedo and M R Teixeira

    MSH6 germline mutations in early-onset colorectal cancer patients without family history of the disease

    advance online publication, 2006-08-29 00:00:00.000;

    doi:10.1038/sj.bjc.6603318

  • F Ficari, A Cama, R Valanzano, M C Curia, R Palmirotta, G Aceto, D L Esposito, S Crognale, A Lombardi, L Messerini, R Mariani-Costantini, F Tonelli and P Battista

    APC gene mutations and colorectal adenomatosis in familial adenomatous polyposis

    doi:10.1054/bjoc.1999.0925

  • A Figer, L Irmin, R Geva, D Flex, A Sulkes and E Friedman

    Genetic analysis of the APC gene regions involved in attenuated APC phenotype in Israeli patients with early onset and familial colorectal cancer

    doi:10.1054/bjoc.2001.1959

  • germline variation

    C R Jekimovs, X Chen, J Arnold, M Gatei, D J Richard, A B Spurdle, K K Khanna and G Chenevix-Trench

    Low frequency of CHEK2 1100delC allele in Australian multiple-case breast cancer families: functional analysis in heterozygous individuals

    advance online publication, 2005-02-08 00:00:00.000;

    doi:10.1038/sj.bjc.6602381

  • gestational age

    M Melbye, J Wohlfahrt, A-M N Andersen, T Westergaard and P K Andersen

    Preterm delivery and risk of breast cancer

    doi:10.1038/sj.bjc.6690399