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Miikka Vikkula

Showing results (61-70 of 199) with videos related to

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Prenatal Diagnosis|October 19, 2005
Hydrops fetalis: an unusual prenatal presentation of hereditary congenital lymphedemaEtty Daniel-Spiegel, Arash Ghalamkarpour, Ronen Spiegel, et al.
The Journal of Clinical Investigation|April 15, 2022
Recalibrating vascular malformations and mechanotransduction by pharmacological interventionSalim Abdelilah-Seyfried, M Luisa Iruela-Arispe, Josef M Penninger, et al.
Nature Reviews. Disease Primers|October 22, 2021
Primary lymphoedemaPascal Brouillard, Marlys H Witte, Robert P Erickson, et al.
European Journal of Human Genetics : EJHG|August 10, 2006
A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?Ilse Gutierrez-Roelens, Luc De Roy, Caroline Ovaert, et al.
HGG Advances|December 29, 2022
Toward reporting standards for the pathogenicity of variant combinations involved in multilocus/oligogenic diseasesSofia Papadimitriou, Barbara Gravel, Charlotte Nachtegael, et al.
Journal of Vascular Anomalies|July 10, 2025
Updated Classification of Vascular Anomalies. A living document from the International Society for the Study of Vascular Anomalies Classification GroupDov Charles Goldenberg, Miikka Vikkula, Anthony Penington, et al.
Human Molecular Genetics|October 7, 2017
Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3Pascal Brouillard, Laura Dupont, Raphael Helaers, et al.
Orphanet Journal of Rare Diseases|May 15, 2024
Targeted treatment in complex lymphatic anomaly: a case of synergistic efficacy of trametinib and sirolimusEmmanuel Seront, Antoine Froidure, Nicole Revencu, et al.
Scientific Reports|July 9, 2017
Efficient activation of the lymphangiogenic growth factor VEGF-C requires the C-terminal domain of VEGF-C and the N-terminal domain of CCBE1Sawan Kumar Jha, Khushbu Rauniyar, Terhi Karpanen, et al.
Pediatric Dermatology|December 8, 2010
Congenital plaque-type glomuvenous malformations associated with fetal pleural effusion and ascitesElisa Goujon, Kelly M Cordoro, Muriel Barat, et al.
Pageof 20

Showing results (61-70 of 199) with videos related to

Sort By:
Pageof 20
Prenatal Diagnosis|October 19, 2005
Hydrops fetalis: an unusual prenatal presentation of hereditary congenital lymphedemaEtty Daniel-Spiegel, Arash Ghalamkarpour, Ronen Spiegel, et al.
The Journal of Clinical Investigation|April 15, 2022
Recalibrating vascular malformations and mechanotransduction by pharmacological interventionSalim Abdelilah-Seyfried, M Luisa Iruela-Arispe, Josef M Penninger, et al.
Nature Reviews. Disease Primers|October 22, 2021
Primary lymphoedemaPascal Brouillard, Marlys H Witte, Robert P Erickson, et al.
European Journal of Human Genetics : EJHG|August 10, 2006
A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?Ilse Gutierrez-Roelens, Luc De Roy, Caroline Ovaert, et al.
HGG Advances|December 29, 2022
Toward reporting standards for the pathogenicity of variant combinations involved in multilocus/oligogenic diseasesSofia Papadimitriou, Barbara Gravel, Charlotte Nachtegael, et al.
Journal of Vascular Anomalies|July 10, 2025
Updated Classification of Vascular Anomalies. A living document from the International Society for the Study of Vascular Anomalies Classification GroupDov Charles Goldenberg, Miikka Vikkula, Anthony Penington, et al.
Human Molecular Genetics|October 7, 2017
Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3Pascal Brouillard, Laura Dupont, Raphael Helaers, et al.
Orphanet Journal of Rare Diseases|May 15, 2024
Targeted treatment in complex lymphatic anomaly: a case of synergistic efficacy of trametinib and sirolimusEmmanuel Seront, Antoine Froidure, Nicole Revencu, et al.
Scientific Reports|July 9, 2017
Efficient activation of the lymphangiogenic growth factor VEGF-C requires the C-terminal domain of VEGF-C and the N-terminal domain of CCBE1Sawan Kumar Jha, Khushbu Rauniyar, Terhi Karpanen, et al.
Pediatric Dermatology|December 8, 2010
Congenital plaque-type glomuvenous malformations associated with fetal pleural effusion and ascitesElisa Goujon, Kelly M Cordoro, Muriel Barat, et al.
Pageof 20