Paediatric lymphoedema: An audit of patients seen by the paediatric and primary lymphoedema group of vascular European Reference Network (VASCERN)

Author:

Devoogdt NeleORCID,Van Zanten Malou,Damstra Robert,Van Duinen Kirsten,Dickinson-Blok Janine L.,Thomis Sarah,Giacalone Guido,Belva Florence,Suominen Sinikka,Kavola Heli,Oberlin Michael,Rossler Jochen,Rucigaj Tanja Planinsek,Riches Katie,Mansour Sahar,Gordon Kristiana,Vignes Stéphane,Keeley Vaughan

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference16 articles.

1. The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review;Atton;Eur. J. Hum. Genet.,2015

2. Primary lymphoedema;Brouillard;Nat. Rev. Dis. Prim.,2021

3. A new classification system for primary lymphatic dysplasias based on phenotype;Connell;Clin. Genet.,2010

4. The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings;Connell;Clin. Genet.,2013

5. General Patient Pathway for Pediatric and Primary Lymphedema: European Reference Network for Rear Vascular Diseases;Damstra,2021

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. The VASCERN PPL working group patient pathway for primary and paediatric lymphoedema;European Journal of Medical Genetics;2024-02

2. Lymphœdèmes primaires des membres;La Presse Médicale Formation;2023-10

3. Update December 2022;Lymphatic Research and Biology;2022-12-01

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