Pediatric lymphatic malformations: evolving understanding and therapeutic options.

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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name

Pediatric lymphatic malformations: evolving understanding and therapeutic options.

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Pediatric lymphatic malformations: evolving understanding and therapeutic options.

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Pediatric lymphatic malformations: evolving understanding and therapeutic options.

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Pediatric lymphatic malformations: evolving understanding and therapeutic options.

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Pediatric lymphatic malformations: evolving understanding and therapeutic options.

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Pediatric lymphatic malformations: evolving understanding and therapeutic options.

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P1476

Pediatric lymphatic malformations: evolving understanding and therapeutic options.

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Ann M Defnet

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Jessica J Kandel

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Naina Bagrodia

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Natalie Gwilliam

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Sonia L Hernandez

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P2860

Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema

Isolated lymphatic endothelial cells transduce growth, survival and migratory signals via the VEGF-C/D receptor VEGFR-3

Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase

A mosaic activating mutation in AKT1 associated with the Proteus syndrome

Somatic mosaic activating mutations in PIK3CA cause CLOVES syndrome

Vascular Anomalies Classification: Recommendations From the International Society for the Study of Vascular Anomalies

Vascular anomalies: classification, imaging characteristics and implications for interventional radiology treatment approaches.

Vascular endothelial growth factor C is required for sprouting of the first lymphatic vessels from embryonic veins

Hyperplasia of lymphatic vessels in VEGF-C transgenic mice

Phenotypic characterization of primary lymphedema

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s00383-016-3867-4

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425-433

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scholarly article

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10.1007/S00383-016-3867-4

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2016-01-27T00:00:00Z

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