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M Vikkula Selected Research

Protein-Tyrosine Kinases (Tyrosine Kinase)

8/2000Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase.

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M Vikkula Research Topics

Disease

4Lymphedema (Milroy Disease)
09/2013 - 08/2000
1Familial Breast Cancer
12/2018
1Renal Insufficiency (Renal Failure)
04/2015
1Hypertension (High Blood Pressure)
04/2015
1Pheochromocytoma
05/2012
1Paraganglioma (Paragangliomas)
05/2012
1Pain (Aches)
10/2010
1Status Epilepticus (Complex Partial Status Epilepticus)
07/2008
1Vascular Malformations
08/2006
1Multiple Cutaneous and Mucosal Venous Malformations
08/2006
1Capillary Malformation-Arteriovenous Malformation
08/2006
1Glomus vagale tumors
08/2006
1Melanoma (Melanoma, Malignant)
06/2000

Drug/Important Bio-Agent (IBA)

1DNA (Deoxyribonucleic Acid)IBA
12/2018
1Proteins (Proteins, Gene)FDA Link
09/2013
1Succinate Dehydrogenase (Fumarate Reductase)IBA
05/2012
1Fibrinogen (Factor I)FDA Link
10/2010
1Low-Molecular-Weight Heparin (Heparin, Low Molecular Weight)IBA
10/2010
1Phosphotransferases (Kinase)IBA
06/2009
1NeuroserpinIBA
07/2008
1Vascular Endothelial Growth Factor Receptor-3 (Flt 4)IBA
10/2006
1AngiopoietinsIBA
08/2006
1TIE-2 Receptor (Receptor, TIE 2)IBA
08/2006
1Protein-Tyrosine Kinases (Tyrosine Kinase)IBA
08/2000
1AntigensIBA
06/2000

Therapy/Procedure

1Kidney Transplantation
04/2015
1Aftercare (After-Treatment)
10/2006