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Journal Abstract Search
638 related items for PubMed ID: 28654575
1. Update on classification and diagnosis of vascular malformations. McCuaig CC. Curr Opin Pediatr; 2017 Aug; 29(4):448-454. PubMed ID: 28654575 [Abstract] [Full Text] [Related]
2. Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Mirzaa G, Graham JM, Keppler-Noreuil K. ; 1993 Aug. PubMed ID: 23946963 [Abstract] [Full Text] [Related]
4. Vascular Anomaly Syndromes in the ISSVA Classification System: Imaging Findings and Role of Interventional Radiology in Management. Wang MX, Kamel S, Elsayes KM, Guillerman RP, Habiba A, Heng L, Revzin M, Mellnick V, Iacobas I, Chau A. Radiographics; 2022 Oct; 42(6):1598-1620. PubMed ID: 36190850 [Abstract] [Full Text] [Related]
5. 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]
10. Lymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CA. Luks VL, Kamitaki N, Vivero MP, Uller W, Rab R, Bovée JV, Rialon KL, Guevara CJ, Alomari AI, Greene AK, Fishman SJ, Kozakewich HP, Maclellan RA, Mulliken JB, Rahbar R, Spencer SA, Trenor CC, Upton J, Zurakowski D, Perkins JA, Kirsh A, Bennett JT, Dobyns WB, Kurek KC, Warman ML, McCarroll SA, Murillo R. J Pediatr; 2015 Apr; 166(4):1048-54.e1-5. PubMed ID: 25681199 [Abstract] [Full Text] [Related]
11. Clinical and sonographic features of pediatric soft-tissue vascular anomalies part 2: vascular malformations. Johnson CM, Navarro OM. Pediatr Radiol; 2017 Aug; 47(9):1196-1208. PubMed ID: 28779187 [Abstract] [Full Text] [Related]
20. 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] Page: [Next] [New Search]