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Pernille Mathiesen Tørring

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Acta Dermato-Venereologica|January 28, 2022
Capillary Malformation-arteriovenous Malformation Type 2: A Case Report and ReviewAnna Trier Heiberg Brix, Pernille Mathiesen Tørring, Anette Bygum
Ugeskrift for Laeger|February 16, 2011
[Diagnosis and treatment of morbus Osler]Anette Drøhse Kjeldsen, Poul Erik Andersen, Pernille Mathiesen Tørring
Orphanet Journal of Rare Diseases|December 15, 2018
Comorbidity among HHT patients and their controls in a 20 years follow-up periodKatrine Saldern Aagaard, Anette Drøhse Kjeldsen, Pernille Mathiesen Tørring, et al.
Ugeskrift for Laeger|October 23, 2025
[Congenital hearing loss in children]Kristianna Mey, Pernille Mathiesen Tørring, Bjarke Edholm, et al.
Orphanet Journal of Rare Diseases|November 24, 2016
20-year follow-up study of Danish HHT patients-survival and causes of deathAnette Kjeldsen, Katrine Saldern Aagaard, Pernille Mathiesen Tørring, et al.
Ugeskrift for Laeger|October 30, 2014
[Juvenile polyposis syndrome is a rare cause of gastrointestinal cancer]Anne Marie Jelsig, Pernille Mathiesen Tørring, Niels Qvist, et al.
Ugeskrift for Laeger|February 8, 2019
[Glomuvenous malformations can be very painful and cause diagnostic challenges]Anna Trier Heiberg Brix, Pernille Mathiesen Tørring, Shailajah Kamaleswaran, et al.
Ugeskrift for Laeger|October 30, 2014
[Juvenile polyposis syndrome is a rare cause of gastrointestinal cancer]Anne Marie Jelsig, Pernille Mathiesen Tørring, Niels Qvist, et al.
Ugeskrift for Laeger|October 30, 2014
[Juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia syndrome in a patient a with SMAD4 mutation]Anne Marie Jelsig, Pernille Mathiesen Tørring, Friedrik Wikman, et al.
Ugeskrift for Laeger|May 1, 2019
[Glomuvenous malformations]Anna Trier Heiberg Brix, Pernille Mathiesen Tørring, Shailajah Kamaleswaran, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Acta Dermato-Venereologica|January 28, 2022
Capillary Malformation-arteriovenous Malformation Type 2: A Case Report and ReviewAnna Trier Heiberg Brix, Pernille Mathiesen Tørring, Anette Bygum
Ugeskrift for Laeger|February 16, 2011
[Diagnosis and treatment of morbus Osler]Anette Drøhse Kjeldsen, Poul Erik Andersen, Pernille Mathiesen Tørring
Orphanet Journal of Rare Diseases|December 15, 2018
Comorbidity among HHT patients and their controls in a 20 years follow-up periodKatrine Saldern Aagaard, Anette Drøhse Kjeldsen, Pernille Mathiesen Tørring, et al.
Ugeskrift for Laeger|October 23, 2025
[Congenital hearing loss in children]Kristianna Mey, Pernille Mathiesen Tørring, Bjarke Edholm, et al.
Orphanet Journal of Rare Diseases|November 24, 2016
20-year follow-up study of Danish HHT patients-survival and causes of deathAnette Kjeldsen, Katrine Saldern Aagaard, Pernille Mathiesen Tørring, et al.
Ugeskrift for Laeger|October 30, 2014
[Juvenile polyposis syndrome is a rare cause of gastrointestinal cancer]Anne Marie Jelsig, Pernille Mathiesen Tørring, Niels Qvist, et al.
Ugeskrift for Laeger|February 8, 2019
[Glomuvenous malformations can be very painful and cause diagnostic challenges]Anna Trier Heiberg Brix, Pernille Mathiesen Tørring, Shailajah Kamaleswaran, et al.
Ugeskrift for Laeger|October 30, 2014
[Juvenile polyposis syndrome is a rare cause of gastrointestinal cancer]Anne Marie Jelsig, Pernille Mathiesen Tørring, Niels Qvist, et al.
Ugeskrift for Laeger|October 30, 2014
[Juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia syndrome in a patient a with SMAD4 mutation]Anne Marie Jelsig, Pernille Mathiesen Tørring, Friedrik Wikman, et al.
Ugeskrift for Laeger|May 1, 2019
[Glomuvenous malformations]Anna Trier Heiberg Brix, Pernille Mathiesen Tørring, Shailajah Kamaleswaran, et al.
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