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Anja Wagner

Showing results (71-80 of 174) with videos related to

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Cancer|April 19, 2007
Biallelic germline mutations of mismatch-repair genes: a possible cause for multiple pediatric malignanciesJan-Werner Poley, Anja Wagner, Monique M C P Hoogmans, et al.
Cancers|February 3, 2021
Gynecological Surveillance and Surgery Outcomes in Dutch Lynch Syndrome CarriersEllis L Eikenboom, Helena C van Doorn, Winand N M Dinjens, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|June 22, 2013
Quality assessment of cardiovascular magnetic resonance in the setting of the European CMR registry: description and validation of standardized criteriaVincenzo Klinke, Stefano Muzzarelli, Nathalie Lauriers, et al.
Scandinavian Journal of Gastroenterology|January 21, 2009
Underutilization of microsatellite instability analysis in colorectal cancer patients at high risk for Lynch syndromeMargot G F Van Lier, Johannes H W De Wilt, Jessie J M F Wagemakers, et al.
Familial Cancer|December 13, 2005
Long term follow-up of HNPCC gene mutation carriers: compliance with screening and satisfaction with counseling and screening proceduresAnja Wagner, Ingrid van Kessel, Mieke G Kriege, et al.
Journal of Pediatric Hematology/Oncology|September 1, 2017
Very Long-term Sequelae After Nonradical Surgery Combined With Brachytherapy in an Infant With a Chemotherapy-resistant Rhabdomyosarcoma of the TonguePetra M van Rijswijk, Marry M van den Heuvel-Eibrink, Erica L T van den Akker, et al.
Cancer|December 15, 2005
American founder mutation for Lynch syndrome. Prevalence estimates and implicationsHenry T Lynch, Albert de la Chapelle, Heather Hampel, et al.
JACC. Cardiovascular Imaging|November 19, 2011
Acute adverse reactions to gadolinium-based contrast agents in CMR: multicenter experience with 17,767 patients from the EuroCMR RegistryOliver Bruder, Steffen Schneider, Detlev Nothnagel, et al.
JAMA|February 12, 2004
A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United StatesHenry T Lynch, Stephanie M Coronel, Ross Okimoto, et al.
Familial Cancer|July 31, 2009
Attitude towards pre-implantation genetic diagnosis for hereditary cancerChantal Lammens, Eveline Bleiker, Neil Aaronson, et al.
Pageof 18

Showing results (71-80 of 174) with videos related to

Sort By:
Pageof 18
Cancer|April 19, 2007
Biallelic germline mutations of mismatch-repair genes: a possible cause for multiple pediatric malignanciesJan-Werner Poley, Anja Wagner, Monique M C P Hoogmans, et al.
Cancers|February 3, 2021
Gynecological Surveillance and Surgery Outcomes in Dutch Lynch Syndrome CarriersEllis L Eikenboom, Helena C van Doorn, Winand N M Dinjens, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|June 22, 2013
Quality assessment of cardiovascular magnetic resonance in the setting of the European CMR registry: description and validation of standardized criteriaVincenzo Klinke, Stefano Muzzarelli, Nathalie Lauriers, et al.
Scandinavian Journal of Gastroenterology|January 21, 2009
Underutilization of microsatellite instability analysis in colorectal cancer patients at high risk for Lynch syndromeMargot G F Van Lier, Johannes H W De Wilt, Jessie J M F Wagemakers, et al.
Familial Cancer|December 13, 2005
Long term follow-up of HNPCC gene mutation carriers: compliance with screening and satisfaction with counseling and screening proceduresAnja Wagner, Ingrid van Kessel, Mieke G Kriege, et al.
Journal of Pediatric Hematology/Oncology|September 1, 2017
Very Long-term Sequelae After Nonradical Surgery Combined With Brachytherapy in an Infant With a Chemotherapy-resistant Rhabdomyosarcoma of the TonguePetra M van Rijswijk, Marry M van den Heuvel-Eibrink, Erica L T van den Akker, et al.
Cancer|December 15, 2005
American founder mutation for Lynch syndrome. Prevalence estimates and implicationsHenry T Lynch, Albert de la Chapelle, Heather Hampel, et al.
JACC. Cardiovascular Imaging|November 19, 2011
Acute adverse reactions to gadolinium-based contrast agents in CMR: multicenter experience with 17,767 patients from the EuroCMR RegistryOliver Bruder, Steffen Schneider, Detlev Nothnagel, et al.
JAMA|February 12, 2004
A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United StatesHenry T Lynch, Stephanie M Coronel, Ross Okimoto, et al.
Familial Cancer|July 31, 2009
Attitude towards pre-implantation genetic diagnosis for hereditary cancerChantal Lammens, Eveline Bleiker, Neil Aaronson, et al.
Pageof 18