Lynchin oireyhtymän syöpää ehkäisevä seuranta muuttuu geenikohtaiseksi

Mecklin, Jukka-Pekka

dc.contributor.author	Mecklin, Jukka-Pekka
dc.date.accessioned	2022-08-17T06:31:45Z
dc.date.available	2022-08-17T06:31:45Z
dc.date.issued	2020
dc.identifier.citation	Mecklin, J.-P. (2020). Lynchin oireyhtymän syöpää ehkäisevä seuranta muuttuu geenikohtaiseksi. <i>Duodecim</i>, <i>137</i>(17), 1867-1869. <a href="https://www.duodecimlehti.fi/lehti/2020/17/duo15749" target="_blank">https://www.duodecimlehti.fi/lehti/2020/17/duo15749</a>
dc.identifier.other	CONVID_148843389
dc.identifier.uri	https://jyx.jyu.fi/handle/123456789/82604
dc.description.abstract	Asetyylisalisyylihapon tehosta vakuuttavaa näyttöä ja rokote kehitteillä	fi
dc.format.mimetype	application/pdf
dc.language.iso	fin
dc.publisher	Kustannus Oy Duodecim
dc.relation.ispartofseries	Duodecim
dc.relation.uri	https://www.duodecimlehti.fi/lehti/2020/17/duo15749
dc.rights	In Copyright
dc.title	Lynchin oireyhtymän syöpää ehkäisevä seuranta muuttuu geenikohtaiseksi
dc.type	article
dc.identifier.urn	URN:NBN:fi:jyu-202208174148
dc.contributor.laitos	Liikuntatieteellinen tiedekunta	fi
dc.contributor.laitos	Faculty of Sport and Health Sciences	en
dc.type.uri	http://purl.org/eprint/type/JournalItem
dc.type.coar	http://purl.org/coar/resource_type/c_0640
dc.description.reviewstatus	nonPeerReviewed
dc.format.pagerange	1867-1869
dc.relation.issn	0301-8989
dc.relation.numberinseries	17
dc.relation.volume	137
dc.type.version	publishedVersion
dc.rights.copyright	© 2020 Duodecim
dc.rights.accesslevel	openAccess	fi
dc.subject.yso	ennaltaehkäisy
dc.subject.yso	hoitomenetelmät
dc.subject.yso	perinnölliset taudit
dc.subject.yso	riskitekijät
dc.subject.yso	syöpätaudit
dc.subject.yso	paksusuolisyöpä
dc.subject.yso	Lynchin oireyhtymä
dc.subject.yso	seuranta
dc.subject.yso	geenivirheet
dc.format.content	fulltext
jyx.subject.uri	http://www.yso.fi/onto/yso/p19552
jyx.subject.uri	http://www.yso.fi/onto/yso/p392
jyx.subject.uri	http://www.yso.fi/onto/yso/p19997
jyx.subject.uri	http://www.yso.fi/onto/yso/p13277
jyx.subject.uri	http://www.yso.fi/onto/yso/p678
jyx.subject.uri	http://www.yso.fi/onto/yso/p5937
jyx.subject.uri	http://www.yso.fi/onto/yso/p23697
jyx.subject.uri	http://www.yso.fi/onto/yso/p17497
jyx.subject.uri	http://www.yso.fi/onto/yso/p146
dc.rights.url	http://rightsstatements.org/page/InC/1.0/?language=en
jyx.fundinginformation	Jukka-Pekka Mecklin: Apuraha (Syöpäsäätiö, VTR, J&A Erkon Säätiö)
dc.type.okm	B1

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Risk-Reducing Gynecological Surgery in Lynch Syndrome : Results of an International Survey from the Prospective Lynch Syndrome Database

Dominguez-Valentin, Mev; Seppälä, Toni T.; Engel, Christoph; Aretz, Stefan; Macrae, Finlay; Winship, Ingrid; Capella, Gabriel; Thomas, Huw; Hovig, Eivind; Nielsen, Maartje; Sijmons, Rolf H.; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria G.; Cavestro, Giulia M.; Mints, Miriam; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Green, Kate; Lalloo, Fiona; Hill, James; Schmiegel, Wolff; Vangala, Deepak; Perne, Claudia; Strauß, Hans-Georg; Tecklenburg, Johanna; Holinski-Feder, Elke; Steinke-Lange, Verena; Mecklin, Jukka-Pekka; Plazzer, John-Paul; Pineda, Marta; Navarro, Matilde; Vidal, Joan B.; Kariv, Revital; Rosner, Guy; Piñero, Tamara A.; Gonzalez, María L.; Kalfayan, Pablo; Sampson, Julian R.; Ryan, Neil A. J.; Evans, D. G.; Møller, Pål; Crosbie, Emma J. (MDPI, 2020)

Purpose: To survey risk-reducing hysterectomy and bilateral salpingo-oophorectomy (BSO) practice and advice regarding hormone replacement therapy (HRT) in women with Lynch syndrome. Methods: We conducted a survey in 31 ...
Lynch syndrome genetics and clinical implications

Peltomäki, Päivi; Nyström, Minna; Mecklin, Jukka-Pekka; Seppälä, Toni, T. (Elsevier BV, 2023)

Lynch syndrome (LS) is one of the most prevalent hereditary cancer syndromes in man and accounts for some 3% of unselected patients with colorectal or endometrial cancer and 10–15% of those with DNA mismatch repair ...
The “unnatural” history of colorectal cancer in Lynch syndrome : lessons from colonoscopy surveillance

Ahadova, Aysel; Seppälä, Toni T.; Engel, Christoph; Gallon, Richard; Burn, John; Holinski‐Feder, Elke; Steinke‐Lange, Verena; Möslein, Gabriela; Nielsen, Maartje; ten Broeke, Sanne; Laghi, Luigi; Dominguez‐Valentin, Mev; Capella, Gabriel; Macrae, Finlay; Scott, Rodney; Hüneburg, Robert; Nattermann, Jacob; Hoffmeister, Michael; Brenner, Hermann; Bläker, Hendrik; von Knebel Doeberit,z Magnus; Sampson, Julian R.; Vasen, Hans; Mecklin, Jukka‐Pekka; Møller, Pål; Kloor, Matthias (Wiley, 2021)

Individuals with Lynch syndrome (LS), one of the most common inherited cancer syndromes, are at increased risk of developing malignancies, in particular colorectal cancer (CRC). Regular colonoscopy with polypectomy is ...
Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment : a report from the prospective Lynch syndrome database

Dominguez-Valentin, Mev; Haupt, Saskia; Seppälä, Toni T.; Sampson, Julian R.; Sunde, Lone; Bernstein, Inge; Jenkins, Mark A.; Engel, Christoph; Aretz, Stefan; Nielsen, Maartje; Capella, Gabriel; Balaguer, Francesc; Evans, Dafydd Gareth; Burn, John; Holinski-Feder, Elke; Bertario, Lucio; Bonanni, Bernardo; Lindblom, Annika; Levi, Zohar; Macrae, Finlay; Winship, Ingrid; Plazzer, John-Paul; Sijmons, Rolf; Laghi, Luigi; Della Valle, Adriana; Heinimann, Karl; Dębniak, Tadeusz; Fruscio, Robert; Lopez-Koestner, Francisco; Alvarez-Valenzuela, Karin; Katz, Lior H.; Laish, Ido; Vainer, Elez; Vaccaro, Carlos; Carraro, Dirce Maria; Monahan, Kevin; Half, Elizabeth; Stakelum, Aine; Winter, Des; Kennelly, Rory; Gluck, Nathan; Sheth, Harsh; Abu-Freha, Naim; Greenblatt, Marc; Rossi, Benedito Mauro; Bohorquez, Mabel; Cavestro, Giulia Martina; Lino-Silva, Leonardo S.; Horisberger, Karoline; Tibiletti, Maria Grazia; do Nascimento, Ivana; Thomas, Huw; Rossi, Norma Teresa; Apolinário da Silva, Leandro; Zaránd, Attila; Ruiz-Bañobre, Juan; Heuveline, Vincent; Mecklin, Jukka-Pekka; Pylvänäinen, Kirsi; Renkonen-Sinisalo, Laura; Lepistö, Anna; Peltomäki, Päivi; Therkildsen, Christina; Madsen, Mia Gebauer; Burgdorf, Stefan Kobbelgaard; Hopper, John L.; Win, Aung Ko; Haile, Robert W.; Lindor, Noralane; Gallinger, Steven; Le Marchand, Loïc; Newcomb, Polly A.; Figueiredo, Jane; Buchanan, Daniel D.; Thibodeau, Stephen N.; von Knebel Doeberitz, Magnus; Loeffler, Markus; Rahner, Nils; Schröck, Evelin; Steinke-Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Perne, Claudia; Hüneburg, Robert; Redler, Silke; Büttner, Reinhard; Weitz, Jürgen; Pineda, Marta; Duenas, Nuria; Vidal, Joan Brunet; Moreira, Leticia; Sánchez, Ariadna; Hovig, Eivind; Nakken, Sigve; Green, Kate; Lalloo, Fiona; Hill, James; Crosbie, Emma; Mints, Miriam; Goldberg, Yael; Tjandra, Douglas; ten Broeke, Sanne W.; Kariv, Revital; Rosner, Guy; Advani, Suresh H.; Thomas, Lidiya; Shah, Pankaj; Shah, Mithun; Neffa, Florencia; Esperon, Patricia; Pavicic, Walter; Torrezan, Giovana Tardin; Bassaneze, Thiago; Martin, Claudia Alejandra; Moslein, Gabriela; Moller, Pål (Elsevier BV, 2023)

Background The Prospective Lynch Syndrome Database (PLSD) collates information on carriers of pathogenic or likely pathogenic MMR variants (path_MMR) who are receiving medical follow-up, including colonoscopy surveillance, ...
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

Seppälä, Toni T.; Ahadova, Aysel; Dominguez-Valentin, Mev; Macrae, Finlay; Evans, D. Gareth; Therkildsen, Christina; Sampson, Julian; Scott, Rodney; Burn, John; Möslein, Gabriela; Bernstein, Inge; Holinski-Feder, Elke; Pylvänäinen, Kirsi; Renkonen-Sinisalo, Laura; Lepistö, Anna; Lautrup, Charlotte Kvist; Lindblom, Annika; Plazzer, John-Paul; Winship, Ingrid; Tjandra, Douglas; Katz, Lior H.; Aretz, Stefan; Hüneburg, Robert; Holzapfel, Stefanie; Heinimann, Karl; Valle, Adriana Della; Neffa, Florencia; Gluck, Nathan; Cappel, Wouter H. de Vos tot Nederveen; Vasen, Hans; Morak, Monika; Steinke-Lange, Verena; Engel, Christoph; Rahner, Nils; Schmiegel, Wolff; Vangala, Deepak; Thomas, Huw; Green, Kate; Lalloo, Fiona; Crosbie, Emma J.; Hill, James; Capella, Gabriel; Pineda, Marta; Navarro, Matilde; Blanco, Ignacio; Broeke, Sanne ten; Nielsen, Maartje; Ljungmann, Ken; Nakken, Sigve; Lindor, Noralane; Frayling, Ian; Hovig, Eivind; Sunde, Lone; Kloor, Matthias; Mecklin, Jukka-Pekka; Kalager, Mette; Møller, Pål (BioMed Central Ltd., 2019)

Background Recent epidemiological evidence shows that colorectal cancer (CRC) continues to occur in carriers of pathogenic mismatch repair (path_MMR) variants despite frequent colonoscopy surveillance in expert centres. ...

Lynchin oireyhtymän syöpää ehkäisevä seuranta muuttuu geenikohtaiseksi

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Aineisto kuuluu seuraaviin kokoelmiin

Samankaltainen aineisto

Risk-Reducing Gynecological Surgery in Lynch Syndrome : Results of an International Survey from the Prospective Lynch Syndrome Database ﻿

Lynch syndrome genetics and clinical implications ﻿

The “unnatural” history of colorectal cancer in Lynch syndrome : lessons from colonoscopy surveillance ﻿

Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment : a report from the prospective Lynch syndrome database ﻿

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 ﻿

Risk-Reducing Gynecological Surgery in Lynch Syndrome : Results of an International Survey from the Prospective Lynch Syndrome Database

Lynch syndrome genetics and clinical implications

The “unnatural” history of colorectal cancer in Lynch syndrome : lessons from colonoscopy surveillance

Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment : a report from the prospective Lynch syndrome database

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