These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
668 related items for PubMed ID: 27607321
1. Genetic basis for vascular anomalies. Kirkorian AY, Grossberg AL, Püttgen KB. Semin Cutan Med Surg; 2016 Sep; 35(3):128-36. PubMed ID: 27607321 [Abstract] [Full Text] [Related]
12. Oral sildenafil as a treatment option for lymphatic malformations in PIK3CA-related tissue overgrowth syndromes. Horbach SE, Jolink F, van der Horst CM. Dermatol Ther; 2016 Nov; 29(6):466-469. PubMed ID: 27502552 [Abstract] [Full Text] [Related]
13. Syndromes associated with vascular tumors and malformations: a pictorial review. Nozaki T, Nosaka S, Miyazaki O, Makidono A, Yamamoto A, Niwa T, Tsutsumi Y, Aida N, Masaki H, Saida Y. Radiographics; 2013 Nov; 33(1):175-95. PubMed ID: 23322836 [Abstract] [Full Text] [Related]
15. Non-hotspot PIK3CA mutations are more frequent in CLOVES than in common or combined lymphatic malformations. Brouillard P, Schlögel MJ, Homayun Sepehr N, Helaers R, Queisser A, Fastré E, Boutry S, Schmitz S, Clapuyt P, Hammer F, Dompmartin A, Weitz-Tuoretmaa A, Laranne J, Pasquesoone L, Vilain C, Boon LM, Vikkula M. Orphanet J Rare Dis; 2021 Jun 10; 16(1):267. PubMed ID: 34112235 [Abstract] [Full Text] [Related]
16. SOLAMEN syndrome with cardiovascular damage. Zhao X, Yue X, Yuan S, Dai Y, Gu H. Hereditas; 2024 Jul 30; 161(1):24. PubMed ID: 39080810 [Abstract] [Full Text] [Related]
18. A PIK3CA mutation in an acquired capillary malformation. Rosenthal J, Sibbald C, Jen M, Deardorff MA, Treat J. Pediatr Dermatol; 2020 Jan 30; 37(1):246-247. PubMed ID: 31830321 [Abstract] [Full Text] [Related]
19. Vascular malformations syndromes: an update. Martinez-Lopez A, Salvador-Rodriguez L, Montero-Vilchez T, Molina-Leyva A, Tercedor-Sanchez J, Arias-Santiago S. Curr Opin Pediatr; 2019 Dec 30; 31(6):747-753. PubMed ID: 31693582 [Abstract] [Full Text] [Related]