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Your search keyword '"Sampson, J.R."' showing total 10 results
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10 results on '"Sampson, J.R."'

1. Peutz-Jeghers syndrome: a systematic review and recommendations for management

Author

Beggs, A.D., Latchford, A.R., Vasen, H.F.A., Moslein, G., Alonso, A., Aretz, S., Bertario, L., Blanco, I., Bulow, S., Burn, J., Capella, G., Colas, C., Friedl, W., Moller, P., Hes, F.J., Jarvinen, H., Mecklin, J.-P., Nagengast, F.M., Parc, Y., Phillips, R.K.S., Hyer, W., Ponz de Leon, M., Renkonen-Sinisalo, L., Sampson, J.R., Stormorken, A., Tejpar, S., Thomas, H.J.W., Wijnen, J.T., Clark, S.K., and Hodgson, S.V.

Subjects
Peutz-Jeghers syndrome -- Diagnosis, Peutz-Jeghers syndrome -- Care and treatment, Peutz-Jeghers syndrome -- Development and progression, Peutz-Jeghers syndrome -- Risk factors, Medical literature -- Analysis, Health
Published
2010

2. Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3

Author

Dallosso, A.R., Dolwani, S., Jones, N., Jones, S., Colley, J., Maynard, J., Idziaszczyk, S., Humphreys, V., Arnold, J., Donaldson, A., Eccles, D., Ellis, A., Evans, D.G., Frayling, I.M., Hes, F.J., Houlston, R.S., Maher, E.R., Nielsen, M., Parry, S., Tyler, E., Moskvina, V., Cheadle, J.P., and Sampson, J.R.

Subjects
Colorectal cancer -- Genetic aspects, Colorectal cancer -- Development and progression, Colorectal cancer -- Research, Colorectal cancer -- Risk factors, Gene mutations -- Analysis, Adenoma -- Genetic aspects, Adenoma -- Risk factors, Adenoma -- Research, Health
Published
2008

3. Guidelines for the clinical management of familial adenomatous polyposis (FAP)

Author

Vasen, H.F.A., Moslein, G., Alonso, A., Aretz, S., Bernstein, I., Bertario, L., Blanco, I., Bulow, S., Burn, J., Capella, G., Colas, C., Engel, C., Frayling, I., Friedl, W., Hes, F.J., Hodgson, S., Jarvinen, H., Mecklin, J.-P., Moller, P., Myrhoi, T., Nagengast, F.M., Parc, Y., Phillips, R., Clark, S.K., Ponz de Leon, M., Renkonen-Sinisalo, L., Sampson, J.R., Stormorken, A., Tejpar, S., Thomas, H.J.W., and Wijnen, J.

Subjects
Polyposis, Familial -- Care and treatment, Practice guidelines (Medicine) -- Evaluation, Colorectal cancer -- Risk factors, Colorectal cancer -- Prevention, Health
Published
2008

4. Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer)

Author

Vasen, H.F.A., Moslein, G., Alonso, A., Bernstein, I., Bertario, L., Blanco, I., Burn, J., Capella, G., Engel, C., Frayling, I., Friedl, W., Hes, F.J., Hodgson, S., Mecklin, J.-P., Moller, P., Nagengast, F., Parc, Y., Renkonen-Sinisalo, L., Sampson, J.R., Stormorken, A., and Wijnen, J.

Subjects
Colorectal cancer -- Care and treatment, Colorectal cancer -- Genetic aspects, Practice guidelines (Medicine) -- Evaluation, Cancer -- Diagnosis, Cancer -- Standards, Health
Published
2007

5. Genotype and psychological phenotype in tuberous sclerosis

Author

Lewis, J.C., Thomas, H.V., Murphy, K.C., and Sampson, J.R.

Subjects
Health
Abstract

J Med Genet 2004;41:203-207. doi: 10.1136/jmg.2003.012757 Tuberous sclerosis complex (TSC, MIM 191090 and 191100) is an autosomal dominant, multisystem disorder characterised by the development of a variety of hamartomatous growths. [...]

Published
2004

6. Beckwith-Wiedemann syndrome and assisted reproduction technology (ART). (Letter to JMG)

Author

Maher, E.R., Brueton, L.A., Bowdin, S.C., Luharia, A., Cooper, W., Cole, T.R., Macdonald, F., Sampson, J.R., Barratt, C.L., Reik, W., and Hawkins, M.M.

Subjects
Birth defects -- Research -- Genetic aspects, Beckwith-Wiedemann syndrome -- Genetic aspects -- Research, Reproductive technology -- Health aspects -- Statistics -- Usage -- Research, Health
Abstract

Beckwith-Wiedemann syndrome (BWS) is a model imprinting disorder resulting from mutations or epimutations affecting imprinted genes on chromosome 11p15.5. (1) The classical clinical features of BWS are macroglossia, pre- and/or [...]

Published
2003

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