Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Anna A. Kattentidt-Mouravieva"'
Publikováno v:
Familial Cancer, 13(3), 391-399. Springer Netherlands
Predictive genetic testing for familial adenomatous polyposis (FAP) is routinely offered to children at-risk from the age of 10 years onwards. Predictive testing for FAP at a younger age is debatable, because of absence of medical benefits. However,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6202eb243ea3732b8d16b2a5550eb6f9
https://pure.eur.nl/en/publications/e719f347-09ee-4d24-b825-0e64eed8f1a2
https://pure.eur.nl/en/publications/e719f347-09ee-4d24-b825-0e64eed8f1a2
Autor:
Ans M.W. van den Ouweland, Anna A. Kattentidt Mouravieva, Max M. van Noesel, Joan N.R. Kromosoeto, Ron Smits, Anja Wagner, Ina R. Geurts-Giele, Hendrikus J. Dubbink, Cees P. van de Ven, Winand N.M. Dinjens, Ronald R. de Krijger
Publikováno v:
European Journal of Cancer, 48(12), 1867-1874. Elsevier Ltd.
Objective: Desmoid tumours are rare mesenchymal tumours with unpredictable progression and high recurrence risk. They can occur sporadically or in association with Familial Adenomatous Polyposis (FAP), which is caused by germline APC mutations. The W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19d3babf49895ada94221345a2981c3f
https://pubmed.ncbi.nlm.nih.gov/22305464
https://pubmed.ncbi.nlm.nih.gov/22305464
Autor:
A. Beishuizen, Kathleen Vanheusden, I. van Kessel, Anna A. Kattentidt-Mouravieva, Johanna C. Escher, Anja Wagner
Publikováno v:
Tijdschrift voor Kindergeneeskunde, 78(1), 28-33. Bohn Stafleu van Loghum
Familiaire adenomateuze polyposis coli (FAP) is een erfelijke aandoening die gepaard gaat met het ontstaan van honderden tot duizenden darmpoliepen en darmkanker, veroorzaakt door kiembaanmutaties in het APC-gen. Vaak ontstaan poliepen al op de kinde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b892155f52a867322199154423169916
https://pure.eur.nl/en/publications/d871d4fb-0593-4de5-952b-46b06c912b5d
https://pure.eur.nl/en/publications/d871d4fb-0593-4de5-952b-46b06c912b5d
Autor:
Van Scherpenzeel M; 1 Laboratory of Genetic, Endocrine and Metabolic Diseases, Radboud University Medical Centre, Nijmegen, The Netherlands., Timal S, Rymen D, Hoischen A, Wuhrer M, Hipgrave-Ederveen A, Grunewald S, Peanne R, Saada A, Edvardson S, Grønborg S, Ruijter G, Kattentidt-Mouravieva A, Brum JM, Freckmann ML, Tomkins S, Jalan A, Prochazkova D, Ondruskova N, Hansikova H, Willemsen MA, Hensbergen PJ, Matthijs G, Wevers RA, Veltman JA, Morava E, Lefeber DJ
Publikováno v:
Brain : a journal of neurology [Brain] 2014 Apr; Vol. 137 (Pt 4), pp. 1030-8. Date of Electronic Publication: 2014 Feb 24.