Zobrazeno 1 - 10
of 162
pro vyhledávání: '"Denise A. Adams"'
Autor:
Lola Zerbib, Sophia Ladraa, Antoine Fraissenon, Charles Bayard, Marina Firpion, Quitterie Venot, Sanela Protic, Clément Hoguin, Amandine Thomas, Sylvie Fraitag, Jean-Paul Duong, Sophie Kaltenbach, Estelle Balducci, Coline Lefevre, Patrick Villarese, Vahid Asnafi, Christine Broissand, Nicolas Goudin, Ivan Nemazanyy, Gwennhael Autret, Bertrand Tavitian, Christophe Legendre, Nadia Arzouk, Veronique Minard-Colin, Caroline Chopinet, Michael Dussiot, Denise M. Adams, Tristan Mirault, Laurent Guibaud, Paul Isenring, Guillaume Canaud
Publikováno v:
Signal Transduction and Targeted Therapy, Vol 9, Iss 1, Pp 1-16 (2024)
Abstract Sporadic venous malformations are genetic conditions primarily caused by somatic gain-of-function mutation of PIK3CA or TEK, an endothelial transmembrane receptor signaling through PIK3CA. Venous malformations are associated with pain, bleed
Externí odkaz:
https://doaj.org/article/0a7680e7260f408ca2c1f17a769785da
Autor:
Michael S Broder, Denise M Adams, Guillame Canaud, Christy Collins, Kristen Davis, Ilona J. Frieden, Sarah N Gibbs, Adrienne M Hammill, Kim M Keppler-Noreuil, Taizo A Nakano, Anthony Penington, Siddharth Srivastava, Megha M Tollefson, Matthew L Warman
Publikováno v:
Journal of Vascular Anomalies, Vol 4, Iss 2, p e067 (2023)
Objective(s):. PIK3CA-related overgrowth spectrum (PROS) is a group of disorders caused by somatic variants in the PIK3CA gene. We aimed to update recommendations on the severity classification, testing, and medical management of patients with PROS.
Externí odkaz:
https://doaj.org/article/d36076aec9cc4f8d86a1a5b1b44fef06
Autor:
Jessica B Foster, Dong Li, Michael E March, Sarah E Sheppard, Denise M Adams, Hakon Hakonarson, Yoav Dori
Publikováno v:
EMBO Molecular Medicine, Vol 12, Iss 10, Pp 1-6 (2020)
Abstract Kaposiform lymphangiomatosis (KLA) is a rare lymphatic anomaly primarily affecting the mediastinum with high mortality rate. We present a patient with KLA and significant disease burden harboring a somatic point mutation in the Casitas B lin
Externí odkaz:
https://doaj.org/article/c7e586d63ea64231bfa3397727caeb93
Autor:
Bede N. Nriagu, Denise M. Adams, Abhay Srinivasan, Ganesh Krishnamurthy, Chris Smith, Yoav Dori, Kristen Snyder
Publikováno v:
Lymphatic Research and Biology. 21:135-140
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
The field of vascular anomalies has grown tremendously in the last few decades with the identification of key molecular pathways and genetic mutations that drive the formation and progression of vascular anomalies. Understanding these pathways is cri
Externí odkaz:
https://doaj.org/article/bc6ef8da74124387944d1d03e1b79570
Autor:
Matthew E. Fertakos, Evelyn M. Beaury, Neil R. Ford, Nicole L. Kinlock, Denise W. Adams, Bethany A. Bradley
Publikováno v:
Ecology.
Autor:
Jeremy M. Grenier, Alexandra J. Borst, Sarah E. Sheppard, Kristen M. Snyder, Dong Li, Lea F. Surrey, Alyaa Al‐Ibraheemi, David R. Weber, James R. Treat, Christopher L. Smith, Pablo Laje, Yoav Dori, Denise M. Adams, Michael Acord, Abhay S. Srinivasan
Publikováno v:
Pediatric Blood & Cancer.
Autor:
Antonio R. Perez-Atayde, Larisa Debelenko, Alyaa Al-Ibraheemi, Whitney Eng, Melisa Ruiz-Gutierrez, Meghan O’Hare, Stacy E. Croteau, Cameron C. Trenor, Debra Boyer, Daniel M. Balkin, Sarah F. Barclay, Belinda Hsi Dickie, Marilyn G. Liang, Gulraiz Chaudry, Ahmad I. Alomari, John B. Mulliken, Denise M. Adams, Kyle C. Kurek, Steven J. Fishman, Harry P.W. Kozakewich
Publikováno v:
American Journal of Surgical Pathology. 46:963-976
Autor:
C. Griffin McDaniel, Denise M. Adams, Kimberley E. Steele, Adrienne M. Hammill, A. Carl Merrow, Janet L. Crane, Christopher L. Smith, Harry P. W. Kozakewich, Timothy D. Le Cras
Publikováno v:
Pediatric Blood & Cancer. 70
Autor:
Olivia Grace, Cohen, Stephanie, Florez-Pollack, Laura S, Finn, Mary, Larijani, Melinda, Jen, James, Treat, Denise M, Adams, Michael R, Acord
Publikováno v:
Pediatrics. 150
Kaposiform hemangioendothelioma is classified as a locally aggressive vascular tumor of childhood resulting from abnormal angiogenesis and lymphangiogenesis. Most commonly, KHE presents as a single tissue mass, ranging from an erythematous papule to