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Pascal Brouillard

Showing results (1-10 of 40) with videos related to

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Human Molecular Genetics|August 3, 2007
Genetic causes of vascular malformationsPascal Brouillard, Miikka Vikkula
The Journal of Clinical Investigation|March 5, 2014
Genetics of lymphatic anomaliesPascal Brouillard, Laurence Boon, Miikka Vikkula
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.
American Journal of Medical Genetics. Part A|April 14, 2021
Hypotrichosis-lymphedema-telangiectasia syndrome: Report of ileal atresia associated with a SOX18 de novo pathogenic variant and review of the phenotypic spectrumRichard Coulie, Dmitriy M Niyazov, Michael J Gambello, et al.
American Journal of Medical Genetics. Part A|July 7, 2021
EPHB4 mutation causes adult and adolescent-onset primary lymphedemaArin K Greene, Pascal Brouillard, Christopher L Sudduth, et al.
Human Mutation|December 22, 2025
Likely Pathogenic/Pathogenic Variants in the Spliceosome Complex Genes SNRNP200, SF3B1, SF3B2, and SF3B4 Implicated in Nonsyndromic Orofacial CleftPeyman Ranji, Eleonore Pairet, Raphael Helaers, 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.
Nature Reviews. Disease Primers|October 22, 2021
Primary lymphoedemaPascal Brouillard, Marlys H Witte, Robert P Erickson, 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.
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.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
Human Molecular Genetics|August 3, 2007
Genetic causes of vascular malformationsPascal Brouillard, Miikka Vikkula
The Journal of Clinical Investigation|March 5, 2014
Genetics of lymphatic anomaliesPascal Brouillard, Laurence Boon, Miikka Vikkula
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.
American Journal of Medical Genetics. Part A|April 14, 2021
Hypotrichosis-lymphedema-telangiectasia syndrome: Report of ileal atresia associated with a SOX18 de novo pathogenic variant and review of the phenotypic spectrumRichard Coulie, Dmitriy M Niyazov, Michael J Gambello, et al.
American Journal of Medical Genetics. Part A|July 7, 2021
EPHB4 mutation causes adult and adolescent-onset primary lymphedemaArin K Greene, Pascal Brouillard, Christopher L Sudduth, et al.
Human Mutation|December 22, 2025
Likely Pathogenic/Pathogenic Variants in the Spliceosome Complex Genes SNRNP200, SF3B1, SF3B2, and SF3B4 Implicated in Nonsyndromic Orofacial CleftPeyman Ranji, Eleonore Pairet, Raphael Helaers, 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.
Nature Reviews. Disease Primers|October 22, 2021
Primary lymphoedemaPascal Brouillard, Marlys H Witte, Robert P Erickson, 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.
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.
Pageof 4