Cardiac Presentation of Rosai-dorfman Disease in a Pediatric Patient

Autor: Sassan Hashemi, MD, Timotheus Watson, MD, Hunter Wilson, MD, Denver Sallee, MD, Timothy Slesnick, MD

Publikováno v: Journal of Cardiovascular Magnetic Resonance, Vol 26, Iss , Pp 100040- (2024)

Externí odkaz: https://doaj.org/article/0303608dd5224949b528c6c07b7f75ed

Rerouting of Cerebral Circulation

Autor: R. Allen Ligon, MD, Denver Sallee, MD, Sassan Hashemi, MD, Clifford M. Hawkins, MD, Christopher J. Petit, MD

Publikováno v: JACC: Case Reports, Vol 2, Iss 6, Pp 855-859 (2020)

We describe an adolescent with long-standing atresia of the head/neck arteries and severe aortic coarctation. Because of progressive symptoms, a series of interventions was undertaken to provide direct aorta–to–carotid artery flow and coarctation

Externí odkaz: https://doaj.org/article/20ad4453f39e45729a34f0aff4dc100d

Clinical History and Management Recommendations of the Smooth Muscle Dysfunction Syndrome Due to ACTA2 Arginine 179 Alterations

Autor: M. Elizabeth Brickner, Reed E. Pyeritz, Kathryn C. Chatfield, Dianna M. Milewicz, Anthony L. Estrera, Ellen S. Regalado, Hiroko Morisaki, Patricia L. Musolino, Lauren Mellor-Crummey, Susan L. Benedict, Mustafa Tekin, Denver Sallee, Kathryn W. Holmes, Timothy J. Bradley, Cori Feist, Glen J. Iannucci, Julie Richer, Sherene Shalhub, John R. Østergaard, Lesley C. Adès, Anne H. Child, Paul R. Mark, Shaine A. Morris, Anna L. Mitchell, Birgit Lorenz, Julie De Backer, Takayuki Morisaki, Anji T. Yetman, Alan C. Braverman

Publikováno v: Genetics in medicine : official journal of the American College of Medical Genetics
Regalado, E S, Mellor-Crummey, L, De Backer, J, Braverman, A C, Ades, L, Benedict, S, Bradley, T J, Brickner, M E, Chatfield, K C, Child, A, Feist, C, Holmes, K W, Iannucci, G, Lorenz, B, Mark, P, Morisaki, T, Morisaki, H, Morris, S A, Mitchell, A L, Ostergaard, J R, Richer, J, Sallee, D, Shalhub, S, Tekin, M, Estrera, A, Musolino, P, Yetman, A, Pyeritz, R, Milewicz, D M & Montalcino Aortic Consortium 2018, ' Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations ', Genetics in Medicine, vol. 20, no. 10, pp. 1206-1215 . https://doi.org/10.1038/gim.2017.245

Purpose: Smooth muscle dysfunction syndrome (SMDS) due to heterozygous ACTA2 arginine 179 alterations is characterized by patent ductus arteriosus, vasculopathy (aneurysm and occlusive lesions), pulmonary arterial hypertension, and other complication

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8781f25dd24c3cd5595fe15cb4a2f568
http://europepmc.org/articles/PMC6034999

Do

Autor: Hannah L, Hanania, Ellen S, Regalado, Dong-Chuan, Guo, Lili, Xu, Erin, Demo, Denver, Sallee, Dianna M, Milewicz

Publikováno v: Circulation. Genomic and precision medicine. 12(12)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4da407d7eeba878632f1232f0e853527
https://pubmed.ncbi.nlm.nih.gov/28254189

Systolic ejection click versus split first heart sound: Are our ears deceiving us?

Autor: Natalie M, Hoeting, Courtney E, McCracken, Michael, McConnell, Denver, Sallee, Glen J, Iannucci, Matthew E, Oster

Publikováno v: Congenital heart disease. 12(4)

Bicuspid aortic valve (BAV) disease is associated with potential lifetime complications, but auscultation of a BAV click is commonly missed or mistaken for a benign split first heart sound. Our objective was to determine whether pediatric cardiologis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::59951ced71c25de323bcd2555ad23d4a
https://pubmed.ncbi.nlm.nih.gov/28299882