Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Britta Halvarsson"'
Autor:
Britta Halvarsson, Anna Rosén, Lars Stenhammar, Carina Lagerqvist, Olof Sandström, Anna Myléus, Fredrik Norström, Lotta Högberg, Anneli Ivarsson, Annelie Carlsson, Charlotta Webb
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 60:787-791
OBJECTIVES: To evaluate any potential correlation between anti-tissue transglutaminase antibodies of type immunoglobulin A (tTG-IgA) and the degree of gluten induced enteropathy in children partici ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7340caa415393767038292f73ec0cff5
https://doi.org/10.1097/mpg.0000000000000688
https://doi.org/10.1097/mpg.0000000000000688
Autor:
Olof Sandström, Charlotta Webb, Anna Myléus, Britta Halvarsson, Lars Danielsson, Eva Karlsson, Lars Stenhammar, Annelie Carlsson, Lotta Högberg, Anneli Ivarsson, Fredrik Norström
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 52:549-553
OBJECTIVES:: In a Swedish celiac disease screening study (Exploring the Iceberg of Celiacs in Sweden), we systematically reviewed the clinical diagnostic procedures with the aim to evaluate the diagnostic accuracy and to take advantage of lessons lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e10294215eb657b52d1c1d84a0f0a91
https://doi.org/10.1097/mpg.0b013e3181fa434f
https://doi.org/10.1097/mpg.0b013e3181fa434f
Autor:
Nickolas Papadopoulos, Päivi Peltomäki, Richard D. Kolodner, Tao Liu, Bert Vogelstein, Kenneth W. Kinzler, Britta Halvarsson, Mef Nilbert, Thierry Frebourg, Kristina Lagerstedt Robinson, Jana Vandrovcova, Mark Clendenning, Annika Lindblom
Publikováno v:
JNCI Journal of the National Cancer Institute. 99:291-299
Background Preventive programs for individuals who have high lifetime risks of colorectal cancer may reduce disease morbidity and mortality. Thus, it is important to identify the factors that are associated with hereditary colorectal cancer and to mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67551a680df1d03b199ba094107f3d40
https://doi.org/10.1093/jnci/djk051
https://doi.org/10.1093/jnci/djk051
Autor:
Peter Mangell, Anna Isinger, Johan Ottosson, Maria Planck, Mef Nilbert, Britta Halvarsson, Wolfram Müller, Magnus Hallén, Anna Clara Benoni
Publikováno v:
Journal of Clinical Pathology. 60:781-786
BACKGROUND: Hereditary non-polyposis colorectal cancer (HNPCC) is associated with high risks for colorectal and endometrial cancer, young age at onset and an increased risk of multiple primary tumours. Colorectal cancer in HNPCC is characterised by p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d2043f779bdf8c89820094017f70d27
https://doi.org/10.1136/jcp.2006.040402
https://doi.org/10.1136/jcp.2006.040402
Autor:
Susanne Malander, Britta Halvarsson, Ulf Kristoffersson, Åke Borg, Eva Rambech, Mef Nilbert, Mona Ridderheim
Publikováno v:
Gynecologic Oncology. 101:238-243
Objective. Ovarian cancer has one of the highest fractions of hereditary cases. The hereditary breast and ovarian cancer syndrome, primarily due to mutations in BRCA1 and BRCA2, is the main cause of heredity, but also the hereditary nonpolyposis colo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b90559c35a7c82ebd353ba811a9e029
https://doi.org/10.1016/j.ygyno.2005.10.029
https://doi.org/10.1016/j.ygyno.2005.10.029
Publikováno v:
Modern Pathology. 18:1095-1101
Colorectal adenomas occur at younger age, at increased frequency and have a greater tendency for malignant transformation in patients with hereditary nonpolyposis colorectal cancer (HNPCC). We performed immunostaining for the mismatch repair proteins
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3daf4f8e46f7d6911cb6c6bb1d35b523
https://doi.org/10.1038/modpathol.3800392
https://doi.org/10.1038/modpathol.3800392
Autor:
Britta Halvarsson, Maria Planck, Mef Nilbert, Zofia Piotrowska, Kajsa Ericson, Eva Rambech, J Nagel, Håkan Olsson
Publikováno v:
European Journal of Cancer. 39:240-248
Individuals with an inherited predisposition to cancer development are at an increased risk of developing multiple tumours. Hereditary non-polyposis colorectal cancer (HNPCC) is one of the most common hereditary cancer syndromes and is estimated to a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca1e37f5b9f54c78db271dcd9793b936
https://doi.org/10.1016/s0959-8049(02)00584-1
https://doi.org/10.1016/s0959-8049(02)00584-1
Publikováno v:
BMC Clinical Pathology
Background: The identification of mismatch-repair (MMR) defective colon cancer is clinically relevant for diagnostic, prognostic and potentially also for treatment predictive purposes. Preselection of tumors for MMR analysis can be obtained with pred
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b966cbfe5530bc4975dd4fa30a92493e
https://doi.org/10.1186/1472-6890-13-33
https://doi.org/10.1186/1472-6890-13-33
Autor:
Anna Rosén, Olof Sandström, Annelie Carlsson, Solveig Hammarroth, Anna Myléus, Maria van der Pals, Lotta Högberg, Lars Danielsson, Eva Karlsson, Lars Stenhammar, Charlotta Webb, Britta Halvarsson, Fredrik Norström, Anneli Ivarsson, Olle Hernell
Publikováno v:
Pediatrics. 131(3)
OBJECTIVES: Between 1984 and 1996, Sweden experienced an “epidemic” of clinical celiac disease in children METHODS: A 2-phase cross-sectional screening study was performed in which 13 279 children from 2 birth cohorts participated: children born
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67c182e2d122c7fca34b76716a202867
https://pubmed.ncbi.nlm.nih.gov/23420914
https://pubmed.ncbi.nlm.nih.gov/23420914
Autor:
Mev Dominguez-Valentin, Ke Borg, Eva Rambech, Christina Therkildsen, Anja Nissen, Göran Jönsson, Britta Halvarsson, Mef Nilbert, Inge Bernstein
Publikováno v:
European journal of cancer (Oxford, England : 1990). 49(6)
Lynch syndrome and familial colorectal cancer type X, FCCTX, represent the two predominant colorectal cancer syndromes. Whereas Lynch syndrome is clinically and genetically well defined, the genetic cause of FCCTX is unknown and genomic differences b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae7e3880f88c88fd9588da0b19d9b3bc
https://pubmed.ncbi.nlm.nih.gov/23245329
https://pubmed.ncbi.nlm.nih.gov/23245329