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Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report

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DOI
10.1186/s13053-019-0106-8
Seppälä, Toni T.; Ahadova, Aysel; Dominguez-Valentin, Mev; Macrae, Finlay; Evans, D. Gareth; Therkil...
Hereditary cancer in clinical practice2019Publicationer information ikon

Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report

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DOI
10.1186/s13053-017-0078-5
Seppala, Toni; Pylvanainen, Kirsi; Evans, Dafydd Gareth; Jarvinen, Heikki; Renkonen-Sinisalo, Laura;...
Hereditary cancer in clinical practice2017Publicationer information ikon

Descriptive study on subjective experience of genetic testing with respect to relationship, family planning and psychosocial wellbeing among women with lynch syndrome

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10.1186/s13053-021-00194-x
Kalamo, Mari; Mäenpää, Johanna; Seppälä, Toni; Mecklin, Jukka-Pekka; Pylvänäinen, Kirsi; Staff, Synn...
Hereditary cancer in clinical practice2021Publicationer information ikon

Colorectal cancer incidences in Lynch syndrome : a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

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DOI
10.1186/s13053-022-00241-1
Møller, Pål; Seppälä, Toni; Dowty, James G.; Haupt, Saskia; Dominguez-Valentin, Mev; Sunde, Lone; Be...
Hereditary cancer in clinical practice2022Publicationer information ikon

Colorectal carcinogenesis in the Lynch syndromes and familial adenomatous polyposis:trigger events and downstream consequences

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10.1186/s13053-025-00305-y
Moller, Pål; Ahadova, Aysel; Kloor, Matthias; Seppälä, Toni T.; Burn, John; Haupt, Saskia; Macrae, F...
Hereditary cancer in clinical practice2025Publicationer information ikon

Age-specific familial risks in cancer as clues to germline genetic and environmental causes:focus on colorectal, endometrial, prostate, kidney, breast and lung cancers

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10.1186/s13053-024-00301-8
Hemminki, Kari; Försti, Asta; Hemminki, Otto; Scott, Rodney J.; Hemminki, Akseli
Hereditary cancer in clinical practice2025Publicationer information ikon

High familial risks in some rare cancers may pinpoint to hidden germline genetics:focus on esophageal, stomach, small intestinal, testis, thyroid and bone cancers

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DOI
10.1186/s13053-024-00303-6
Hemminki, Kari; Hemminki, Otto; Koskinen, Anni; Hemminki, Akseli; Försti, Asta
Hereditary cancer in clinical practice2025Publicationer information ikon

Incidences of colorectal adenomas and cancers under colonoscopy surveillance suggest an accelerated “Big Bang” pathway to CRC in three of the four Lynch syndromes

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DOI
10.1186/s13053-024-00279-3
Møller, Pål; Haupt, Saskia; Ahadova, Aysel; Kloor, Matthias; Sampson, Julian R.; Sunde, Lone; Seppäl...
Hereditary cancer in clinical practice2024Publicationer information ikon

Dominantly inherited micro-satellite instable cancer – the four Lynch syndromes - an EHTG, PLSD position statement

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DOI
10.1186/s13053-023-00263-3
Møller, Pal; Seppälä, Toni T.; Ahadova, Aysel; Crosbie, Emma J.; Holinski-Feder, Elke; Scott, Rodney...
HEREDITARY CANCER IN CLINICAL PRACTICE2023Publicationer information ikon

Informing patients about their mutation tests:CDKN2A c.256G>A in melanoma as an example

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DOI
10.1186/s13053-020-00146-x
Hemminki, Kari; Srivastava, Aayushi; Rachakonda, Sivaramakrishna; Bandapalli, Obul; Nagore, Eduardo;...
Hereditary cancer in clinical practice2020

Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report

Referentgranskad
Öppen tillgång
DOI
10.1186/s13053-019-0106-8
2019

Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report

Referentgranskad
Öppen tillgång
DOI
10.1186/s13053-017-0078-5
2017

Descriptive study on subjective experience of genetic testing with respect to relationship, family planning and psychosocial wellbeing among women with lynch syndrome

Referentgranskad
Öppen tillgång
DOI
10.1186/s13053-021-00194-x
2021

Colorectal cancer incidences in Lynch syndrome : a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

Referentgranskad
Öppen tillgång
DOI
10.1186/s13053-022-00241-1
2022

Colorectal carcinogenesis in the Lynch syndromes and familial adenomatous polyposis:trigger events and downstream consequences

Referentgranskad
Öppen tillgång
DOI
10.1186/s13053-025-00305-y
2025

Age-specific familial risks in cancer as clues to germline genetic and environmental causes:focus on colorectal, endometrial, prostate, kidney, breast and lung cancers

Referentgranskad
Öppen tillgång
DOI
10.1186/s13053-024-00301-8
2025

High familial risks in some rare cancers may pinpoint to hidden germline genetics:focus on esophageal, stomach, small intestinal, testis, thyroid and bone cancers

Referentgranskad
Öppen tillgång
DOI
10.1186/s13053-024-00303-6
2025

Incidences of colorectal adenomas and cancers under colonoscopy surveillance suggest an accelerated “Big Bang” pathway to CRC in three of the four Lynch syndromes

Referentgranskad
Öppen tillgång
DOI
10.1186/s13053-024-00279-3
2024

Dominantly inherited micro-satellite instable cancer – the four Lynch syndromes - an EHTG, PLSD position statement

Referentgranskad
Öppen tillgång
DOI
10.1186/s13053-023-00263-3
2023

Informing patients about their mutation tests:CDKN2A c.256G>A in melanoma as an example

Referentgranskad
Öppen tillgång
DOI
10.1186/s13053-020-00146-x
2020