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Cerebrospinal fluid biomarker and brain biopsy findings in idiopathic normal pressure hydrocephalus. [electronic resource] by
- Pyykkö, Okko T
- Lumela, Miikka
- Rummukainen, Jaana
- Nerg, Ossi
- Seppälä, Toni T
- Herukka, Sanna-Kaisa
- Koivisto, Anne M
- Alafuzoff, Irina
- Puli, Lakshman
- Savolainen, Sakari
- Soininen, Hilkka
- Jääskeläinen, Juha E
- Hiltunen, Mikko
- Zetterberg, Henrik
- Leinonen, Ville
Producer: 20150113
In:
PloS one vol. 9
Availability: No items available.
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10.
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Exome and immune cell score analyses reveal great variation within synchronous primary colorectal cancers. [electronic resource] by
- Hänninen, Ulrika A
- Wirta, Erkki-Ville
- Katainen, Riku
- Tanskanen, Tomas
- Hamberg, Jiri
- Taipale, Minna
- Böhm, Jan
- Renkonen-Sinisalo, Laura
- Lepistö, Anna
- Forsström, Linda M
- Pitkänen, Esa
- Palin, Kimmo
- Seppälä, Toni T
- Mäkinen, Netta
- Mecklin, Jukka-Pekka
- Aaltonen, Lauri A
Producer: 20200228
In:
British journal of cancer vol. 120
Availability: No items available.
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11.
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Amyloid-β and Tau Dynamics in Human Brain Interstitial Fluid in Patients with Suspected Normal Pressure Hydrocephalus. [electronic resource] by
- Herukka, Sanna-Kaisa
- Rummukainen, Jaana
- Ihalainen, Jouni
- von Und Zu Fraunberg, Mikael
- Koivisto, Anne M
- Nerg, Ossi
- Puli, Lakshman K
- Seppälä, Toni T
- Zetterberg, Henrik
- Pyykkö, Okko T
- Helisalmi, Seppo
- Tanila, Heikki
- Alafuzoff, Irina
- Hiltunen, Mikko
- Rinne, Jaakko
- Soininen, Hilkka
- Jääskeläinen, Juha E
- Leinonen, Ville
Producer: 20160627
In:
Journal of Alzheimer's disease : JAD vol. 46
Availability: No items available.
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12.
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Cancer risk and survival in [electronic resource] by
- Møller, Pål
- Seppälä, Toni T
- Bernstein, Inge
- Holinski-Feder, Elke
- Sala, Paulo
- Gareth Evans, D
- Lindblom, Annika
- Macrae, Finlay
- Blanco, Ignacio
- Sijmons, Rolf H
- Jeffries, Jacqueline
- Vasen, Hans F A
- Burn, John
- Nakken, Sigve
- Hovig, Eivind
- Rødland, Einar Andreas
- Tharmaratnam, Kukatharmini
- de Vos Tot Nederveen Cappel, Wouter H
- Hill, James
- Wijnen, Juul T
- Jenkins, Mark A
- Green, Kate
- Lalloo, Fiona
- Sunde, Lone
- Mints, Miriam
- Bertario, Lucio
- Pineda, Marta
- Navarro, Matilde
- Morak, Monika
- Renkonen-Sinisalo, Laura
- Valentin, Mev Dominguez
- Frayling, Ian M
- Plazzer, John-Paul
- Pylvanainen, Kirsi
- Genuardi, Maurizio
- Mecklin, Jukka-Pekka
- Moeslein, Gabriela
- Sampson, Julian R
- Capella, Gabriel
Producer: 20180720
In:
Gut vol. 67
Availability: No items available.
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13.
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Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome. [electronic resource] by
- Engel, Christoph
- Ahadova, Aysel
- Seppälä, Toni T
- Aretz, Stefan
- Bigirwamungu-Bargeman, Marloes
- Bläker, Hendrik
- Bucksch, Karolin
- Büttner, Reinhard
- de Vos Tot Nederveen Cappel, Wouter T
- Endris, Volker
- Holinski-Feder, Elke
- Holzapfel, Stefanie
- Hüneburg, Robert
- Jacobs, Maarten A J M
- Koornstra, Jan J
- Langers, Alexandra M
- Lepistö, Anna
- Morak, Monika
- Möslein, Gabriela
- Peltomäki, Päivi
- Pylvänäinen, Kirsi
- Rahner, Nils
- Renkonen-Sinisalo, Laura
- Schulmann, Karsten
- Steinke-Lange, Verena
- Stenzinger, Albrecht
- Strassburg, Christian P
- van de Meeberg, Paul C
- van Kouwen, Mariette
- van Leerdam, Monique
- Vangala, Deepak B
- Vecht, Juda
- Verhulst, Marie-Louise
- von Knebel Doeberitz, Magnus
- Weitz, Jürgen
- Zachariae, Silke
- Loeffler, Markus
- Mecklin, Jukka-Pekka
- Kloor, Matthias
- Vasen, Hans F
Producer: 20200710
In:
Gastroenterology vol. 158
Availability: No items available.
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14.
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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. [electronic resource] by
- 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
- de Vos Tot Nederveen Cappel, Wouter H
- 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
- Ten Broeke, Sanne
- Nielsen, Maartje
- Ljungmann, Ken
- Nakken, Sigve
- Lindor, Noralane
- Frayling, Ian
- Hovig, Eivind
- Sunde, Lone
- Kloor, Matthias
- Mecklin, Jukka-Pekka
- Kalager, Mette
- Møller, Pål
Publication details: Hereditary cancer in clinical practice 2019
In:
Hereditary cancer in clinical practice vol. 17
Availability: No items available.
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15.
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Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database. [electronic resource] by
- Dominguez-Valentin, Mev
- Sampson, Julian R
- Seppälä, Toni T
- Ten Broeke, Sanne W
- Plazzer, John-Paul
- Nakken, Sigve
- Engel, Christoph
- Aretz, Stefan
- Jenkins, Mark A
- Sunde, Lone
- Bernstein, Inge
- Capella, Gabriel
- Balaguer, Francesc
- Thomas, Huw
- Evans, D Gareth
- Burn, John
- Greenblatt, Marc
- Hovig, Eivind
- de Vos Tot Nederveen Cappel, Wouter H
- Sijmons, Rolf H
- Bertario, Lucio
- Tibiletti, Maria Grazia
- Cavestro, Giulia Martina
- Lindblom, Annika
- Della Valle, Adriana
- Lopez-Köstner, Francisco
- Gluck, Nathan
- Katz, Lior H
- Heinimann, Karl
- Vaccaro, Carlos A
- Büttner, Reinhard
- Görgens, Heike
- Holinski-Feder, Elke
- Morak, Monika
- Holzapfel, Stefanie
- Hüneburg, Robert
- Knebel Doeberitz, Magnus von
- Loeffler, Markus
- Rahner, Nils
- Schackert, Hans K
- Steinke-Lange, Verena
- Schmiegel, Wolff
- Vangala, Deepak
- Pylvänäinen, Kirsi
- Renkonen-Sinisalo, Laura
- Hopper, John L
- Win, Aung Ko
- Haile, Robert W
- Lindor, Noralane M
- Gallinger, Steven
- Le Marchand, Loïc
- Newcomb, Polly A
- Figueiredo, Jane C
- Thibodeau, Stephen N
- Wadt, Karin
- Therkildsen, Christina
- Okkels, Henrik
- Ketabi, Zohreh
- Moreira, Leticia
- Sánchez, Ariadna
- Serra-Burriel, Miquel
- Pineda, Marta
- Navarro, Matilde
- Blanco, Ignacio
- Green, Kate
- Lalloo, Fiona
- Crosbie, Emma J
- Hill, James
- Denton, Oliver G
- Frayling, Ian M
- Rødland, Einar Andreas
- Vasen, Hans
- Mints, Miriam
- Neffa, Florencia
- Esperon, Patricia
- Alvarez, Karin
- Kariv, Revital
- Rosner, Guy
- Pinero, Tamara Alejandra
- Gonzalez, María Laura
- Kalfayan, Pablo
- Tjandra, Douglas
- Winship, Ingrid M
- Macrae, Finlay
- Möslein, Gabriela
- Mecklin, Jukka-Pekka
- Nielsen, Maartje
- Møller, Pål
Producer: 20200608
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 22
Availability: No items available.
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