Kristiana Gordon Selected Research

Ligands

8/2018	A Novel Splice-Site Mutation in VEGFC Is Associated with Congenital Primary Lymphoedema of Gordon.
3/2013	Mutation in vascular endothelial growth factor-C, a ligand for vascular endothelial growth factor receptor-3, is associated with autosomal dominant milroy-like primary lymphedema.

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Kristiana Gordon Research Topics

Disease

4	Lymphedema (Milroy Disease) 08/2018 - 03/2013
2	Hydrops Fetalis (Fetal Edema) 01/2021 - 01/2016
2	Vascular Malformations 11/2018 - 01/2018
1	Inborn Genetic Diseases (Disease, Hereditary) 01/2022
1	Arteriovenous Malformations (Arteriovenous Malformation) 01/2021
1	Neoplasms (Cancer) 01/2018
1	Necrosis 04/2017
1	Cardiofaciocutaneous syndrome 05/2016
1	Noonan Syndrome (Female Pseudo-Turner Syndrome) 05/2016
1	Perinatal Death 01/2016
1	Edema (Dropsy) 09/2015
1	hereditary Xerocytosis 09/2015

Drug/Important Bio-Agent (IBA)

2	Mitogen-Activated Protein KinasesIBA 01/2022 - 05/2016
2	Vascular Endothelial Growth Factor Receptor-3 (Flt 4)IBA 08/2018 - 03/2013
2	LigandsIBA 08/2018 - 03/2013
2	Phosphotransferases (Kinase)IBA 05/2016 - 01/2016
1	EphrinsIBA 01/2021
1	Pharmaceutical PreparationsIBA 08/2017
1	EphA1 Receptor (Eph Receptor)IBA 01/2016
1	Ion Channels (Ion Channel)IBA 09/2015
1	Vascular Endothelial Growth Factor A (Vascular Endothelial Growth Factor)IBA 03/2013
1	Vascular Endothelial Growth Factor CIBA 03/2013

Therapy/Procedure

4	Therapeutics 11/2018 - 04/2017
1	Operative Surgical Procedures 10/2014
1	Radiotherapy 10/2014
1	Lymph Node Excision (Lymph Node Dissection) 10/2014
1	Palliative Care (Palliative Therapy) 10/2014