131 related articles for article (PubMed ID: 35807022)
1. Nosological and Theranostic Approach to Vascular Malformation through cfDNA NGS Liquid Biopsy.
Serio VB; Palmieri M; Loberti L; Granata S; Fallerini C; Vaghi M; Renieri A; Pinto AM
J Clin Med; 2022 Jun; 11(13):. PubMed ID: 35807022
[TBL] [Abstract][Full Text] [Related]
2. Cell-free DNA next-generation sequencing liquid biopsy as a new revolutionary approach for arteriovenous malformation.
Palmieri M; Currò A; Tommasi A; Di Sarno L; Doddato G; Baldassarri M; Frullanti E; Giliberti AR; Fallerini C; Spinazzola A; Pinto AM; Renieri A; Vaghi M
JVS Vasc Sci; 2020; 1():176-180. PubMed ID: 34617046
[TBL] [Abstract][Full Text] [Related]
3. MET somatic activating mutations are responsible for lymphovenous malformation and can be identified using cell-free DNA next generation sequencing liquid biopsy.
Palmieri M; Di Sarno L; Tommasi A; Currò A; Doddato G; Baldassarri M; Frullanti E; Giliberti A; Fallerini C; Arzini A; Pinto A; Vaghi M; Renieri A
J Vasc Surg Venous Lymphat Disord; 2021 May; 9(3):740-744. PubMed ID: 32858245
[TBL] [Abstract][Full Text] [Related]
4. A pilot study of next generation sequencing-liquid biopsy on cell-free DNA as a novel non-invasive diagnostic tool for Klippel-Trenaunay syndrome.
Palmieri M; Pinto AM; di Blasio L; Currò A; Monica V; Sarno LD; Doddato G; Baldassarri M; Frullanti E; Giliberti A; Mussolin B; Fallerini C; Molinaro F; Vaghi M; Renieri A; Primo L
Vascular; 2021 Feb; 29(1):85-91. PubMed ID: 32588787
[TBL] [Abstract][Full Text] [Related]
5. Case report: PIK3CA somatic mutation leading to Klippel Trenaunay Syndrome and multiple tumors.
Serio VB; Palmieri M; Innamorato S; Loberti L; Fallerini C; Ariani F; Antolini E; Covarelli J; Vaghi M; Frullanti E; Renieri A; Pinto AM
Front Genet; 2023; 14():1213283. PubMed ID: 37662840
[TBL] [Abstract][Full Text] [Related]
6. Clinical and Molecular Spectrum of Sporadic Vascular Malformations: A Single-Center Study.
Diociaiuti A; Rotunno R; Pisaneschi E; Cesario C; Carnevale C; Condorelli AG; Rollo M; Di Cecca S; Quintarelli C; Novelli A; Zambruno G; El Hachem M
Biomedicines; 2022 Jun; 10(6):. PubMed ID: 35740480
[TBL] [Abstract][Full Text] [Related]
7. Diagnosis and Treatment of Venous Malformations. Consensus Document of the International Union of Phlebology (IUP): updated 2013.
Lee BB; Baumgartner I; Berlien P; Bianchini G; Burrows P; Gloviczki P; Huang Y; Laredo J; Loose DA; Markovic J; Mattassi R; Parsi K; Rabe E; Rosenblatt M; Shortell C; Stillo F; Vaghi M; Villavicencio L; Zamboni P;
Int Angiol; 2015 Apr; 34(2):97-149. PubMed ID: 24566499
[TBL] [Abstract][Full Text] [Related]
8. Evaluation of a Targeted Next-Generation Sequencing Panel for the Non-Invasive Detection of Variants in Circulating DNA of Colorectal Cancer.
Rodríguez-Casanova A; Bao-Caamano A; Lago-Lestón RM; Brozos-Vázquez E; Costa-Fraga N; Ferreirós-Vidal I; Abdulkader I; Vidal-Insua Y; Rivera FV; Candamio Folgar S; López-López R; Muinelo-Romay L; Diaz-Lagares A
J Clin Med; 2021 Sep; 10(19):. PubMed ID: 34640513
[TBL] [Abstract][Full Text] [Related]
9. 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; 16(1):267. PubMed ID: 34112235
[TBL] [Abstract][Full Text] [Related]
10. Cell-free DNA as a diagnostic analyte for molecular diagnosis of vascular malformations.
Zenner K; Jensen DM; Cook TT; Dmyterko V; Bly RA; Ganti S; Mirzaa GM; Dobyns WB; Perkins JA; Bennett JT
Genet Med; 2021 Jan; 23(1):123-130. PubMed ID: 32884133
[TBL] [Abstract][Full Text] [Related]
11. The utility of cerebrospinal fluid-derived cell-free DNA in molecular diagnostics for the
Chen WL; Pao E; Owens J; Glass I; Pritchard C; Shirts BH; Lockwood C; Mirzaa GM
Cold Spring Harb Mol Case Stud; 2022 Apr; 8(3):. PubMed ID: 35483878
[TBL] [Abstract][Full Text] [Related]
12. Genetic landscape of common venous malformations in the head and neck.
Du Z; Liu JL; You YH; Wang LZ; He J; Zheng JW; Zhang ZY; Wang YA
J Vasc Surg Venous Lymphat Disord; 2021 Jul; 9(4):1007-1016.e7. PubMed ID: 33248299
[TBL] [Abstract][Full Text] [Related]
13. Guideline. Diagnosis and treatment of venous malformations. consensus document of the international union of phlebology (iup): updated-2013.
Lee BB; Baumgartner I; Berlien P; Bianchini G; Burrows P; Gloviczki P; Huang Y; Laredo J; Loose DA; Markovic J; Mattassi R; Parsi K; Rabe E; Rosenblatt M; Shortell C; Stillo F; Vaghi M; Villavicencio L; Zamboni P
Int Angiol; 2014 Jun; ():. PubMed ID: 24961611
[TBL] [Abstract][Full Text] [Related]
14. Vascular Birthmarks as a Clue for Complex and Syndromic Vascular Anomalies.
Diociaiuti A; Paolantonio G; Zama M; Alaggio R; Carnevale C; Conforti A; Cesario C; Dentici ML; Buonuomo PS; Rollo M; El Hachem M
Front Pediatr; 2021; 9():730393. PubMed ID: 34692608
[TBL] [Abstract][Full Text] [Related]
15. Characteristics, clinical presentation, and treatment outcomes of venous malformation in the extremities.
Kim H; Joh J; Labropoulos N
J Vasc Surg Venous Lymphat Disord; 2022 Jan; 10(1):152-158. PubMed ID: 34091104
[TBL] [Abstract][Full Text] [Related]
16. Pelvic vascular malformations.
Christenson BM; Gipson MG; Smith MT
Semin Intervent Radiol; 2013 Dec; 30(4):364-71. PubMed ID: 24436563
[TBL] [Abstract][Full Text] [Related]
17. The potential of PIK3CA, KRAS, BRAF, and APC hotspot mutations as a non-invasive detection method for colorectal cancer.
Alizadeh-Sedigh M; Mahmoodzadeh H; Fazeli MS; Haddadi-Aghdam M; Teimoori-Toolabi L
Mol Cell Probes; 2022 Jun; 63():101807. PubMed ID: 35296442
[TBL] [Abstract][Full Text] [Related]
18. Detection of somatic mutations in peritoneal lavages and plasma of endometrial cancer patients: A proof-of-concept study.
Mayo-de-Las-Casas C; Velasco A; Sanchez D; Martínez-Bueno A; Garzón-Ibáñez M; Gatius S; Ruiz-Miró M; Gonzalez-Tallada X; Llordella I; Tresserra F; Rodríguez S; Aldeguer E; Roman-Canal B; Bertran-Alamillo J; García-Peláez B; Rosell R; Molina-Vila MA; Matias-Guiu X
Int J Cancer; 2020 Jul; 147(1):277-284. PubMed ID: 31953839
[TBL] [Abstract][Full Text] [Related]
19. Molecular diagnostic characteristics based on the next generation sequencing in lung cancer and its relationship with the expression of PD-L1.
Liu J; Liu Y
Pathol Res Pract; 2020 Feb; 216(2):152797. PubMed ID: 31926773
[TBL] [Abstract][Full Text] [Related]
20. Fractionated small cell-free DNA increases possibility to detect cancer-related gene mutations in advanced colorectal cancer.
Ishida Y; Takano S; Maekawa S; Yamaguchi T; Yoshida T; Kobayashi S; Iwamoto F; Kuno T; Hayakawa H; Matsuda S; Fukasawa M; Shindo H; Inoue T; Nakayama Y; Ichikawa D; Sato T; Enomoto N
JGH Open; 2020 Oct; 4(5):978-986. PubMed ID: 33102773
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]