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Pediatric Dermatology|July 18, 2020
Kaposiform hemangioendothelioma with overlapping features of rapidly involuting congenital hemangioma and a delayed complication of necrotizing fasciitisLina Belmesk, Josée Dubois, Louise Caouette-Laberge, et al.Journal of Cutaneous Medicine and Surgery|February 15, 2022
Pediatric Cutaneous Hematologic Disorders: Cutaneous Lymphoma and Leukemia Cutis-Experience of a Tertiary-Care Pediatric Institution and Review of the LiteratureCaroline Colmant, Marc-André Demers, Afshin Hatami, et al.Journal of the American Academy of Dermatology|June 29, 2012
Connective tissue nevi in children: institutional experience and reviewCatherine C McCuaig, Caridad Vera, Victor Kokta, et al.Aging Cell|March 25, 2010
Ionizing radiation-induced long-term expression of senescence markers in mice is independent of p53 and immune statusOanh N L Le, Francis Rodier, Francois Fontaine, et al.Journal of Clinical Medicine|May 14, 2025
F18-FDG PET-CT Findings in Juvenile-Onset Polyarteritis Nodosa: A First Series and Literature ReviewClément Triaille, Sebastien Benali, Julie Barsalou, et al.The Canadian Journal of Cardiology|July 8, 2015
Aortic Dilatation Associated With a De Novo Mutation in the SOX18 Gene: Expanding the Clinical Spectrum of Hypotrichosis-Lymphedema-Telangiectasia SyndromeFlorian Wünnemann, Victor Kokta, Séverine Leclerc, et al.Experimental and Therapeutic Medicine|November 22, 2012
Propranolol treatment of infantile hemangioma endothelial cells: A molecular analysisJessica Stiles, Clarissa Amaya, Robert Pham, et al.Plos One|April 5, 2013
Targeting of beta adrenergic receptors results in therapeutic efficacy against models of hemangioendothelioma and angiosarcomaJessica M Stiles, Clarissa Amaya, Steven Rains, et al.The Journal of Biological Chemistry|April 20, 2011
Fetal cardiac troponin isoforms rescue the increased Ca2+ sensitivity produced by a novel double deletion in cardiac troponin T linked to restrictive cardiomyopathy: a clinical, genetic, and functional approachJose Renato Pinto, Shi Wei Yang, Marc-Phillip Hitz, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 26, 2017
A Novel PGM3 Mutation Is Associated With a Severe Phenotype of Bone Marrow Failure, Severe Combined Immunodeficiency, Skeletal Dysplasia, and Congenital MalformationsGuillermo Pacheco-Cuéllar, Julie Gauthier, Valérie Désilets, et al.Pageof 5