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Miikka Vikkula

Showing results (41-50 of 199) with videos related to

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Human Mutation|July 12, 2002
Progressive AV-block and anomalous venous return among cardiac anomalies associated with two novel missense mutations in the CSX/NKX2-5 geneIlse Gutierrez-Roelens, Thierry Sluysmans, Marc Gewillig, et al.
American Journal of Clinical Dermatology|June 20, 2020
New and Emerging Targeted Therapies for Vascular MalformationsAn Van Damme, Emmanuel Seront, Valérie Dekeuleneer, et al.
International Journal of Molecular Sciences|June 9, 2018
Genomics of Fibromuscular DysplasiaSilvia Di Monaco, Adrien Georges, Jean-Philippe Lengelé, et al.
The Journal of Investigative Dermatology|March 24, 2020
Theranostic Advances in Vascular MalformationsValérie Dekeuleneer, Emmanuel Seront, An Van Damme, et al.
Journal of Human Genetics|August 23, 2006
Wide clinical spectrum in a family with hereditary lymphedema type I due to a novel missense mutation in VEGFR3Ronen Spiegel, Arash Ghalamkarpour, Etty Daniel-Spiegel, et al.
Orphanet Journal of Rare Diseases|December 10, 2025
Personalized sirolimus regimen for vascular malformations: a retrospective analysis of VASE cohortEmmanuel Seront, An Van Damme, Julien Coulie, et al.
Expert Review of Clinical Pharmacology|March 8, 2026
Current and emerging pharmacotherapies for treating vascular malformationsEmmanuel Seront, An Van Damme, Julien Coulie, et al.
Critical Reviews in Oncology/Hematology|December 10, 2016
Routine use of gene panel testing in hereditary breast cancer should be performed with cautionCedric van Marcke, Anne De Leener, Martine Berlière, et al.
Gene Expression Patterns : GEP|April 1, 2004
Glomulin is predominantly expressed in vascular smooth muscle cells in the embryonic and adult mouseBrendan A S McIntyre, Pascal Brouillard, Virginie Aerts, et al.
Orphanet Journal of Rare Diseases|July 9, 2021
A review of mechanisms of disease across PIK3CA-related disorders with vascular manifestationsGuillaume Canaud, Adrienne M Hammill, Denise Adams, et al.
Pageof 20

Showing results (41-50 of 199) with videos related to

Sort By:
Pageof 20
Human Mutation|July 12, 2002
Progressive AV-block and anomalous venous return among cardiac anomalies associated with two novel missense mutations in the CSX/NKX2-5 geneIlse Gutierrez-Roelens, Thierry Sluysmans, Marc Gewillig, et al.
American Journal of Clinical Dermatology|June 20, 2020
New and Emerging Targeted Therapies for Vascular MalformationsAn Van Damme, Emmanuel Seront, Valérie Dekeuleneer, et al.
International Journal of Molecular Sciences|June 9, 2018
Genomics of Fibromuscular DysplasiaSilvia Di Monaco, Adrien Georges, Jean-Philippe Lengelé, et al.
The Journal of Investigative Dermatology|March 24, 2020
Theranostic Advances in Vascular MalformationsValérie Dekeuleneer, Emmanuel Seront, An Van Damme, et al.
Journal of Human Genetics|August 23, 2006
Wide clinical spectrum in a family with hereditary lymphedema type I due to a novel missense mutation in VEGFR3Ronen Spiegel, Arash Ghalamkarpour, Etty Daniel-Spiegel, et al.
Orphanet Journal of Rare Diseases|December 10, 2025
Personalized sirolimus regimen for vascular malformations: a retrospective analysis of VASE cohortEmmanuel Seront, An Van Damme, Julien Coulie, et al.
Expert Review of Clinical Pharmacology|March 8, 2026
Current and emerging pharmacotherapies for treating vascular malformationsEmmanuel Seront, An Van Damme, Julien Coulie, et al.
Critical Reviews in Oncology/Hematology|December 10, 2016
Routine use of gene panel testing in hereditary breast cancer should be performed with cautionCedric van Marcke, Anne De Leener, Martine Berlière, et al.
Gene Expression Patterns : GEP|April 1, 2004
Glomulin is predominantly expressed in vascular smooth muscle cells in the embryonic and adult mouseBrendan A S McIntyre, Pascal Brouillard, Virginie Aerts, et al.
Orphanet Journal of Rare Diseases|July 9, 2021
A review of mechanisms of disease across PIK3CA-related disorders with vascular manifestationsGuillaume Canaud, Adrienne M Hammill, Denise Adams, et al.
Pageof 20