K
Kristiana Gordon
Researcher at St George's Hospital
Publications - 17
Citations - 596
Kristiana Gordon is an academic researcher from St George's Hospital. The author has contributed to research in topics: Lymphatic system & Turner syndrome. The author has an hindex of 8, co-authored 17 publications receiving 404 citations. Previous affiliations of Kristiana Gordon include St George’s University Hospitals NHS Foundation Trust & Great Ormond Street Hospital.
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Journal ArticleDOI
Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy
L. Al-Olabi,Satyamaanasa Polubothu,Satyamaanasa Polubothu,Katherine Dowsett,Katrina A. Andrews,Paulina Stadnik,Agnel Praveen Joseph,Rachel G. Knox,Rachel G. Knox,Alan Pittman,Graeme R. Clark,W. Baird,Neil W. Bulstrode,M. Glover,Kristiana Gordon,Darren Hargrave,Susan M Huson,Thomas S. Jacques,Gregory James,Hannah C. Kondolf,Loshan Kangesu,Kim M. Keppler-Noreuil,Amjad Khan,Marjorie J. Lindhurst,Mark H. Lipson,Sahar Mansour,Justine O'Hara,Caroline Mahon,Anda Mosica,Celia Moss,Aditi Murthy,Juling Ong,Victoria E. R. Parker,Victoria E. R. Parker,Jean-Baptiste Rivière,Julie C. Sapp,Neil J. Sebire,Rahul Shah,Branavan Sivakumar,Anna C. Thomas,Alex Virasami,Regula Waelchli,Zhiqiang Zeng,Leslie G. Biesecker,Alex M. Barnacle,Maya Topf,Robert K. Semple,Robert K. Semple,Robert K. Semple,E. Elizabeth Patton,Veronica A. Kinsler,Veronica A. Kinsler +51 more
TL;DR: These findings uncover a major cause of sporadic VMs of different clinical types and thereby offer the potential of personalized medical treatment by repurposing existing licensed cancer therapies.
Journal ArticleDOI
Lipedema: an inherited condition.
Anne H. Child,Kristiana Gordon,Pip Sharpe,Glen Brice,Pia Ostergaard,Steve Jeffery,Peter S. Mortimer +6 more
TL;DR: It is proposed that lipedema is a genetic condition with either X‐linked dominant inheritance or more likely, autosomal dominant inheritance with sex limitation, and appears to be a condition almost exclusively affecting females, presumably estrogen‐requiring as it usually manifests at puberty.
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The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome
Sarah Joyce,Kristiana Gordon,Glen Brice,Pia Ostergaard,Rani Nagaraja,John P. Short,Sandra Moore,Peter S. Mortimer,Sahar Mansour +8 more
TL;DR: This work describes 11 patients with Noonan or CFC syndrome with significant, persistent and progressive lymphatic dysplasia, and demonstrates reflux and/or rerouting of lymphatic drainage associated with incompetent veins on the venous duplex scans.
Journal ArticleDOI
Lymph vessels: the forgotten second circulation in health and disease
Lukasz A. Adamczyk,Kristiana Gordon,Ivana Kholová,Lorine B. Meijer-Jorna,Niklas Telinius,Patrick J. Gallagher,Allard C. van der Wal,Ulrik Baandrup +7 more
TL;DR: This work has shown that immune markers that recognize lymphatic endothelium antigens, such as podoplanin, LYVE-1 and Prox-1, can be successfully applied in diagnostic pathology and have revealed (at least partial) lymphatic differentiation in many types of vascular lesions.
Journal ArticleDOI
The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review.
Giles Atton,Kristiana Gordon,G Brice,Vaughan Keeley,Katie Riches,Pia Ostergaard,Peter S. Mortimer,Sahar Mansour +7 more
TL;DR: The lymphoscintigraphy results suggest that the lymphatic phenotype of Turner syndrome may be due to a failure of initial lymphatic (capillary) function.