Effect of Aspirin or Resistant Starch on Colorectal Neoplasia in the Lynch Syndrome von Burn, John, Bishop, D. Timothy, Mecklin, Jukka-Pekka, Macrae, Finlay, Möslein, Gabriela, Olschwang, Sylviane, Bisgaard, Marie-Luise, Ramesar, Raj, Eccles, Diana, Maher, Eamonn R, Bertario, Lucio, Jarvinen, Heikki J, Lindblom, Annika, Evans, D. Gareth, Lubinski, Jan, Morrison, Patrick J, Ho, Judy W.C, Vasen, Hans F.A, Side, Lucy, Thomas, Huw J.W, Scott, Rodney J, Dunlop, Malcolm, Barker, Gail, Elliott, Faye, Jass, Jeremy R, Fodde, Ricardo, Lynch, Henry T, Mathers, John C

Volltext

Mutual exclusion of ASXL1 and NPM1 mutations in a series of acute myeloid leukemias von Carbuccia, N, Trouplin, V, Gelsi-Boyer, V, Murati, A, Rocquain, J, Adélaïde, J, Olschwang, S, Xerri, L, Vey, N, Chaffanet, M, Birnbaum, D, Mozziconacci, M J

Volltext

NCOA3, a new fusion partner for MOZ/MYST3 in M5 acute myeloid leukemia von Esteyries, S, Perot, C, Adelaide, J, Imbert, M, Lagarde, A, Pautas, C, Olschwang, S, Birnbaum, D, Chaffanet, M, Mozziconacci, M-J

Volltext

Consideration surrounding incidental findings throughout multigene panel testing in cancer genetics von Grandval, P., Fabre, A.J., Béroud, C., Olschwang, S.

Volltext

Molecular patterns in deficient mismatch repair colorectal tumours: results from a French prospective multicentric biological and genetic study von Etienne-Grimaldi, M-C, Mahamat, A, Chazal, M, Laurent-Puig, P, Olschwang, S, Gaub, M-P, Formento, J-L, Formento, P, Sudaka, A, Boige, V, Abderrahim-Ferkoune, A, Benchimol, D, André, T, Houry, S, Faucheron, J-L, Letoublon, C, Gilly, F-N, Delpero, J-R, Lasser, P, Pradere, B, Pezet, D, Penault-Llorca, F, Milano, G

Volltext

Lack of referral for genetic counseling and testing in BRCA1/2 and Lynch syndromes: a nationwide study based on 240,134 consultations and 134,652 genetic tests von Pujol, P., Lyonnet, D. Stoppa, Frebourg, T., Blin, J., Picot, M. C., Lasset, C., Dugast, C., Berthet, P., de Paillerets, B. Bressac, Sobol, H., Grandjouan, S., Soubrier, F., Buecher, B., Guimbaud, R., Lidereau, R., Jonveaux, P., Houdayer, C., Giraud, S., Olschwang, S., Nogue, E., Galibert, V., Bara, C., Nowak, F., Khayat, D., Nogues, C.

Volltext

Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma von OLSCHWANG, Sylviane, BOISSON, Cécile, THOMAS, Gilles

Volltext

The location of constitutional neurofibromatosis 2 (NF2) splice site mutations is associated with the severity of NF2 von Baser, M E, Kuramoto, L, Woods, R, Joe, H, Friedman, J M, Wallace, A J, Ramsden, R T, Olschwang, S, Bijlsma, E, Kalamarides, M, Papi, L, Kato, R, Carroll, J, Lázaro, C, Joncourt, F, Parry, D M, Rouleau, G A, Evans, D G R

Volltext

Cancer risk in 348 French MSH2 or MLH1 gene carriers von Parc, Y, Boisson, C, Thomas, G, Olschwang, S

Volltext

Germline mutations of the APC gene in patients with familial adenomatous polyposis-associated thyroid carcinoma : Results from a european cooperative study von CETTA, F, MONTALTO, G, GORI, M, CURIA, M. C, CAMA, A, OLSCHWANG, S

Volltext

Tissue microarray technology: validation in colorectal carcinoma and analysis of p53, hMLH1, and hMSH2 immunohistochemical expression von Jourdan, Florence, Sebbagh, Nicole, Comperat, Eva, Mourra, Najat, Flahault, Antoine, Olschwang, Sylviane, Duval, Alex, Hamelin, Richard, Flejou, Jean-François

Volltext

First large rearrangement in the MUTYH gene and attenuated familial adenomatous polyposis syndrome von Rouleau, E, Zattara, H, Lefol, C, Noguchi, T, Briaux, A, Buecher, B, Bourdon, V, Sobol, H, Lidereau, R, Olschwang, S

Volltext

Genome profiling of acute myelomonocytic leukemia: alteration of the MYB locus in MYST3-linked cases von Murati, A, Gervais, C, Carbuccia, N, Finetti, P, Cervera, N, Adélaïde, J, Struski, S, Lippert, E, Mugneret, F, Tigaud, I, Penther, D, Bastard, C, Poppe, B, Speleman, F, Baranger, L, Luquet, I, Cornillet-Lefebvre, P, Nadal, N, Nguyen-Khac, F, Pérot, C, Olschwang, S, Bertucci, F, Chaffanet, M, Lessard, M, Mozziconacci, M-J, Birnbaum, D

Volltext

MULTIPLE DURAL LESIONS MIMICKING MENINGIOMAS IN PATIENTS WITH CCM3/ PDCD10 MUTATIONS von LABAUGE, P, FONTAINE, B, OLSCHWANG, S, DENIER, C, TOURNIER-LASSERVE, E, NEAU, J.-P, BERGAMETTI, F, RIANT, F, BLECON, A, MARCHELLI, F, ARNOULT, M, LANNUZEL, A, CLANET, M

Volltext

PD-0608: Risk of metastasis and death in rectal cancer is increased with 8p deletion but not with gene expression von Doyen, J, Letouzé, E, Marisa, L, De Reyniès, A, Milano, G, Etienne-Grimaldi, M, Selves, J, Chapet, O, Olschwang, S, Gérard, J

Volltext

Frequent intragenic rearrangements of DPYD in colorectal tumours von van Kuilenburg, A B P, Etienne-Grimaldi, M-C, Mahamat, A, Meijer, J, Laurent-Puig, P, Olschwang, S, Gaub, M-P, Hennekam, R C M, Benchimol, D, Houry, S, Letoublon, C, Gilly, F-N, Pezet, D, Andre, T, Faucheron, J-L, Abderrahim-Ferkoune, A, Vijzelaar, R, Pradere, B, Milano, G

Volltext

Colon-specific phenotype in Lynch syndrome associated with EPCAM deletion von Grandval, P, Baert-Desurmont, S, Bonnet, F, Bronner, M, Buisine, M-P, Colas, C, Noguchi, T, North, M-O, Rey, J-M, Tinat, J, Toulas, C, Olschwang, S

Volltext

Germline mutation and genome instability von Olschwang, S

Volltext

Turcot syndrome confirmed with molecular analysis von Lebrun, C., Olschwang, S., Jeannin, S., Vandenbos, F., Sobol, H., Frenay, M.

Volltext

Intraductal papillary and mucinous pancreatic tumour: a new extracolonic tumour in familial adenomatous polyposis von Maire, F, Hammel, P, Terris, B, Olschwang, S, O'Toole, D, Sauvanet, A, Palazzo, L, Ponsot, P, Laplane, B, Lévy, P, Ruszniewski, P

Volltext