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Author/Creator Hes, F J

1. Cryptic von Hippel-Lindau disease: germline mutations in patients with haemangioblastoma only. Issue 12 (1st December 2000)

Authors:
Hes, F J; McKee, S; Taphoorn, M J B; Rehal, P; van der Luijt, R B; McMahon, R; van der Smagt, J J; Dow, D; Zewald, R A; Whittaker, J; Lips, C J M; MacDonald, F; Pearson, P L; Maher, E R
Journal:
Journal of medical genetics
Issue:
Volume 37:Issue 12(2000)
Page Start:
939
Record Type:
Journal Article
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4. Guidelines for the clinical management of familial adenomatous polyposis (FAP). Issue 5 (14th January 2008)

Authors:
Vasen, H F A; Möslein, G; Alonso, A; Aretz, S; Bernstein, I; Bertario, L; Blanco, I; Bülow, S; Burn, J; Capella, G; Colas, C; Engel, C; Frayling, I; Friedl, W; Hes, F J; Hodgson, S; Järvinen, H; Mecklin, J-P; Møller, P; Myrhøi, T
Journal:
Gut
Issue:
Volume 57:Issue 5(2008)
Page Start:
704
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

5. Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer). Issue 6 (27th February 2007)

Authors:
Vasen, H F A; Möslein, 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; Møller, P; Nagengast, F; Parc, Y; Renkonen-Sinisalo, L; Sampson, J R; Stormorken, A
Journal:
Journal of medical genetics
Issue:
Volume 44:Issue 6(2007)
Page Start:
353
Record Type:
Journal Article
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6. Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3. Issue 9 (30th May 2008)

Authors:
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
Journal:
Gut
Issue:
Volume 57:Issue 9(2008)
Page Start:
1252
Record Type:
Journal Article
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7. Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP). Issue 9 (1st September 2005)

Authors:
Nielsen, M; Franken, P F; Reinards, T H C M; Weiss, M M; Wagner, A; van der Klift, H; Kloosterman, S; Houwing-Duistermaat, J J; Aalfs, C M; Ausems, M G E M; Bröcker-Vriends, A H J T; Gomez Garcia, E B; Hoogerbrugge, N; Menko, F H; Sijmons, R H; Verhoef, S; Kuipers, E J; Morreau, H; Breuning, M H;...
Journal:
Journal of medical genetics
Issue:
Volume 42:Issue 9(2005)
Page Start:
e54
Record Type:
Journal Article
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8. Nationwide study of patients with head and neck paragangliomas carrying SDHB germline mutations. Issue 2 (6th February 2018)

Authors:
Rijken, J A; Niemeijer, N D; Leemans, C R; Eijkelenkamp, K; van der Horst-Schrivers, A N A; van Berkel, A; Timmers, H J L M; Kunst, H P M; Bisschop, P H L T; van Dooren, M F; Hes, F J; Jansen, J C; Corssmit, E P M; Hensen, E F
Journal:
BJS open
Issue:
Volume 2:Issue 2(2018)
Page Start:
62
Record Type:
Journal Article
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10. Peutz–Jeghers syndrome: a systematic review and recommendations for management. Issue 7 (25th June 2010)

Authors:
Beggs, A D; Latchford, A R; Vasen, H F A; Moslein, G; Alonso, A; Aretz, S; Bertario, L; Blanco, I; Bülow, S; Burn, J; Capella, G; Colas, C; Friedl, W; Møller, P; Hes, F J; Järvinen, H; Mecklin, J-P; Nagengast, F M; Parc, Y; Phillips, R K S
Journal:
Gut
Issue:
Volume 59:Issue 7(2010)
Page Start:
975
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗