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Journal of Lipid Research|January 17, 2013
Micrometric segregation of fluorescent membrane lipids: relevance for endogenous lipids and biogenesis in erythrocytesLudovic D'Auria, Marisa Fenaux, Paulina Aleksandrowicz, et al.Blood Pressure|May 14, 2020
Assessment of adherence to diuretics and β-blockers by serum drug monitoring in comparison to urine analysisSabrina Ritscher, Coralie Georges, Cora Wunder, et al.American Journal of Hypertension|June 28, 2023
From Fibromuscular Dysplasia to Arterial Dissection and BackJustine Huart, Maria S Stoenoiu, Marialuisa Zedde, et al.Human Molecular Genetics|August 31, 2015
Common and specific effects of TIE2 mutations causing venous malformationsMarjut Nätynki, Jaakko Kangas, Ilkka Miinalainen, et al.Journal of Medical Genetics|December 8, 2021
Biallelic <i>ANGPT2</i> loss-of-function causes severe early-onset non-immune hydrops fetalisMarie F Smeland, Pascal Brouillard, Trine Prescott, et al.Nature Cardiovascular Research|August 28, 2024
Case report study of thalidomide therapy in 18 patients with severe arteriovenous malformationsLaurence M Boon, Valérie Dekeuleneer, Julien Coulie, et al.Archives of Dermatology|July 19, 2006
Congenital plaque-type glomuvenous malformations presenting in childhoodSusan Bayliss Mallory, Odile Enjolras, Laurence M Boon, et al.The Journal of Pediatrics|April 28, 2009
Sporadic in utero generalized edema caused by mutations in the lymphangiogenic genes VEGFR3 and FOXC2Arash Ghalamkarpour, Christian Debauche, Eric Haan, et al.Cancer|June 19, 2009
Expression profiling of ependymomas unravels localization and tumor grade-specific tumorigenesisThomas Palm, Dominique Figarella-Branger, Françoise Chapon, et al.American Journal of Medical Genetics. Part A|March 13, 2012
Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutationMatthew G Butler, Susan L Dagenais, José L Garcia-Perez, et al.Pageof 32