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Bibi Lange

Showing results (11-20 of 21) with videos related to

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Orphanet Journal of Rare Diseases|November 14, 2023
The bleeding diathesis in patients with hereditary haemorrhagic telangiectasia is not due to impaired platelet functionAnne Lørup Lyster, Signe Hedengran Biørn, Anette Drøhse Kjeldsen, et al.
Ugeskrift for Laeger|October 23, 2025
[Septal deviation]Kumanan Rune Nanthan, Skala Dehlair Kalid, Peter Schousboe, et al.
Clinical Neurology and Neurosurgery|February 19, 2026
Cerebral vascular malformation screening in hereditary hemorrhagic telangiectasia: Balancing low diagnostic yield against high-risk hemorrhageMikkel Seremet Kofoed, Pernille Mathiesen Tørring, Alex Alban Christensen, et al.
Plos One|November 13, 2012
Complement defects in patients with chronic rhinosinusitisMaria Q Gaunsbaek, Bibi Lange, Anette D Kjeldsen, et al.
Ugeskrift for Laeger|May 17, 2021
[Screening for cerebral arteriovenous malformations in patients with hereditary haemorrhagic telangiectasia]Simon Kjær Simonsen, Troels Halfeld Nielsen, Rikke Beese Dalby, et al.
Clinical Neurology and Neurosurgery|April 8, 2026
When findings hurt: Mental health effects of cerebral MRI screening in patients with Hereditary Hemorrhagic TelangiectasiaMikkel Seremet Kofoed, Pernille Mathiesen Tørring, Alex Alban Christensen, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|August 10, 2018
Dietary patterns and respiratory health in adults from nine European countries-Evidence from the GA<sup>2</sup> LEN studyIoannis Bakolis, Richard Hooper, Claus Bachert, et al.
Ugeskrift for Laeger|June 20, 2025
[Hereditary haemorrhagic telangeiectasia]Kumanan Rune Nanthan, Pernille Mathiesen Tørring, Jens Kjeldsen, et al.
European Journal of Human Genetics : EJHG|October 30, 2025
Multiple lesion-specific somatic mutations and bi-allelic loss of ACVRL1 in a single patient with hereditary haemorrhagic telangiectasiaPernille Darre Haahr, Qin Hao, Klaus Brusgaard, et al.
Frontiers in Allergy|January 29, 2026
Global airways: a Danish nationwide real-life registry of biologic therapy for chronic rhinosinusitis with nasal polypsVibeke Backer, Kasper Aanæs, Bent Ivan Larsen, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Orphanet Journal of Rare Diseases|November 14, 2023
The bleeding diathesis in patients with hereditary haemorrhagic telangiectasia is not due to impaired platelet functionAnne Lørup Lyster, Signe Hedengran Biørn, Anette Drøhse Kjeldsen, et al.
Ugeskrift for Laeger|October 23, 2025
[Septal deviation]Kumanan Rune Nanthan, Skala Dehlair Kalid, Peter Schousboe, et al.
Clinical Neurology and Neurosurgery|February 19, 2026
Cerebral vascular malformation screening in hereditary hemorrhagic telangiectasia: Balancing low diagnostic yield against high-risk hemorrhageMikkel Seremet Kofoed, Pernille Mathiesen Tørring, Alex Alban Christensen, et al.
Plos One|November 13, 2012
Complement defects in patients with chronic rhinosinusitisMaria Q Gaunsbaek, Bibi Lange, Anette D Kjeldsen, et al.
Ugeskrift for Laeger|May 17, 2021
[Screening for cerebral arteriovenous malformations in patients with hereditary haemorrhagic telangiectasia]Simon Kjær Simonsen, Troels Halfeld Nielsen, Rikke Beese Dalby, et al.
Clinical Neurology and Neurosurgery|April 8, 2026
When findings hurt: Mental health effects of cerebral MRI screening in patients with Hereditary Hemorrhagic TelangiectasiaMikkel Seremet Kofoed, Pernille Mathiesen Tørring, Alex Alban Christensen, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|August 10, 2018
Dietary patterns and respiratory health in adults from nine European countries-Evidence from the GA<sup>2</sup> LEN studyIoannis Bakolis, Richard Hooper, Claus Bachert, et al.
Ugeskrift for Laeger|June 20, 2025
[Hereditary haemorrhagic telangeiectasia]Kumanan Rune Nanthan, Pernille Mathiesen Tørring, Jens Kjeldsen, et al.
European Journal of Human Genetics : EJHG|October 30, 2025
Multiple lesion-specific somatic mutations and bi-allelic loss of ACVRL1 in a single patient with hereditary haemorrhagic telangiectasiaPernille Darre Haahr, Qin Hao, Klaus Brusgaard, et al.
Frontiers in Allergy|January 29, 2026
Global airways: a Danish nationwide real-life registry of biologic therapy for chronic rhinosinusitis with nasal polypsVibeke Backer, Kasper Aanæs, Bent Ivan Larsen, et al.
Pageof 3