Reply: Capecitabine and mitomycin C in patients with metastatic colorectal cancer resistant to fluorouracil and irinotecan

Yazar: Chong, G, Cunningham, D
Baskı/Yayın Bilgisi 2006

Using bevacizumab with different chemotherapeutic regimens in metastatic colorectal cancer: balancing utility with low toxicity

Yazar: Chong, G., Tebbutt, N. C.
Baskı/Yayın Bilgisi 2010

Determination of methaemalbumin in plasma.

Yazar: Chong, G C, Owen, J A
Baskı/Yayın Bilgisi 1967

Pharmacological studies on the heart of Tapes watlingi: a mollusc of the family Veneridae.

Yazar: Chong, G C, Phillis, J W
Baskı/Yayın Bilgisi 1965

Endoscopic retrograde cholangiopancreatography in the treatment of intraoperatively demonstrated choledocholithiasis

Yazar: Lynn, AP, Chong, G, Thomson, A
Yayımlandı Ann R Coll Surg Engl (2014)

The HNPCC associated MSH2*1906G→C founder mutation probably originated between 1440 CE and 1715 CE in the Ashkenazi Jewish population

Yazar: Sun, S, Greenwood, C, Thiffault, I, Hamel, N, Chong, G, Foulkes, W
Baskı/Yayın Bilgisi 2005

Ileostomy with ileal reservoir rather than ileostomy alone.

Yazar: Beahrs, O H, Kelly, K A, Adson, M A, Chong, G C
Baskı/Yayın Bilgisi 1974

Disruption of an exon splicing enhancer in exon 3 of MLH1 is the cause of HNPCC in a Quebec family

Yazar: McVety, S, Li, L, Gordon, P H, Chong, G, Foulkes, W D
Baskı/Yayın Bilgisi 2006

Current management of pheochromocytoma.

Yazar: Remine, W H, Chong, G C, Van Heerden, J A, Sheps, S G, Harrison, E G
Baskı/Yayın Bilgisi 1974

The prognostic role of WHO classification, urinary 5-hydroxyindoleacetic acid and liver function tests in metastatic neuroendocrine carcinomas of the gastroenteropancreatic tract

Yazar: Formica, V, Wotherspoon, A, Cunningham, D, Norman, A R, Sirohi, B, Oates, J, Chong, G
Baskı/Yayın Bilgisi 2007

EGFR and K-ras gene mutation status in squamous cell anal carcinoma: a role for concurrent radiation and EGFR inhibitors?

Yazar: Paliga, A, Onerheim, R, Gologan, A, Chong, G, Spatz, A, Niazi, T, Garant, A, Macheto, D, Alcindor, T, Vuong, T
Baskı/Yayın Bilgisi 2012

Diagnostic Performance of Galactomannan Antigen Testing in Cerebrospinal Fluid

Yazar: Chong, G. M., Maertens, J. A., Lagrou, K., Driessen, G. J., Cornelissen, J. J., Rijnders, B. J. A.
Yayımlandı J Clin Microbiol (2016)

EGFR tyrosine kinase mutation testing in the treatment of non-small-cell lung cancer

Yazar: Kamel–Reid, S., Chong, G., Ionescu, D.N., Magliocco, A.M., Spatz, A., Tsao, M., Weng, X., Young, S., Zhang, T., Soulieres, D.
Baskı/Yayın Bilgisi 2012

Capecitabine and mitomycin C as third-line therapy for patients with metastatic colorectal cancer resistant to fluorouracil and irinotecan

Yazar: Chong, G, Dickson, J L B, Cunningham, D, Norman, A R, Rao, S, Hill, M E, Price, T J, Oates, J, Tebbutt, N
Baskı/Yayın Bilgisi 2005

Extensive DNA methylation in normal colorectal mucosa in hyperplastic polyposis

Yazar: Minoo, P, Baker, K, Goswami, R, Chong, G, Foulkes, W D, Ruszkiewicz, A R, Barker, M, Buchanan, D, Young, J, Jass, J R
Baskı/Yayın Bilgisi 2006

Using a family history questionnaire to identify adult patients with increased genetic risk for sarcoma

Yazar: Schiavi, A., Lavigne, J., Turcotte, R., Kasprzak, L., Dumas, N., Chong, G., Freeman, C., Alameldin, M., Galiatsatos, P., Palma, L., Foulkes, W.D.
Yayımlandı Curr Oncol (2015)

Electrical conductivity as a driver of biological and geological spatial heterogeneity in the Puquios, Salar de Llamara, Atacama Desert, Chile

Yazar: Reid, R. P., Oehlert, A. M., Suosaari, E. P., Demergasso, C., Chong, G., Escudero, L. V., Piggot, A. M., Lascu, I., Palma, A. T.
Yayımlandı Sci Rep (2021)

An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1

Yazar: Hutter, P, Wijnen, J, Rey-Berthod, C, Thiffault, I, Verkuijlen, P, Farber, D, Hamel, N, Bapat, B, Thibodeau, S, Burn, J, Wu, J, MacNamara, E, Heinimann, K, Chong, G, Foulkes, W
Baskı/Yayın Bilgisi 2002

Germline truncating mutations in both MSH2 and BRCA2 in a single kindred

Yazar: Thiffault, I, Hamel, N, Pal, T, McVety, S, Marcus, V A, Farber, D, Cowie, S, Deschênes, J, Meschino, W, Odefrey, F, Goldgar, D, Graham, T, Narod, S, Watters, A K, MacNamara, E, Sart, D Du, Chong, G, Foulkes, W D
Baskı/Yayın Bilgisi 2004

The Founder Mutation MSH2*1906G→C Is an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Ashkenazi Jewish Population

Yazar: Foulkes, W. D., Thiffault, I., Gruber, S. B., Horwitz, M., Hamel, N., Lee, C., Shia, J., Markowitz, A., Figer, A., Friedman, E., Farber, D., Greenwood, C. M. T., Bonner, J. D., Nafa, K., Walsh, T., Marcus, V., Tomsho, L., Gebert, J., Macrae, F. A., Gaff, C. L., Paillerets, B. Bressac-de, Gregersen, P. K., Weitzel, J. N., Gordon, P. H., MacNamara, E., King, M.-C., Hampel, H., de la Chapelle, A., Boyd, J., Offit, K., Rennert, G., Chong, G., Ellis, N. A.
Baskı/Yayın Bilgisi 2002