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European Journal of Human Genetics : EJHG|August 6, 2015
The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndromeSarah Joyce, Kristiana Gordon, Glen Brice, et al.Journal of Medical Genetics|May 16, 2020
Update and audit of the St George's classification algorithm of primary lymphatic anomalies: a clinical and molecular approach to diagnosisKristiana Gordon, Ruth Varney, Vaughan Keeley, et al.Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|November 16, 2004
Double-blind placebo-controlled randomised trial of vitamin E and pentoxifylline in patients with chronic arm lymphoedema and fibrosis after surgery and radiotherapy for breast cancerLone Gothard, Paul Cornes, Judith Earl, et al.Frontiers in Immunology|November 29, 2023
Profound and selective lymphopaenia in primary lymphatic anomaly patients demonstrates the significance of lymphatic-lymphocyte interactionsJulian Pearce, Linda Hadcocks, Sahar Mansour, et al.Lymphatic Research and Biology|March 23, 2011
Molecular characterization of dermal lymphatic endothelial cells from primary lymphedema skinSamuel Ogunbiyi, Ganessen Chinien, Della Field, et al.Human Genetics|November 14, 2009
Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasiaFiona Connell, Kamini Kalidas, Pia Ostergaard, et al.Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|April 6, 2004
Non-randomised phase II trial of hyperbaric oxygen therapy in patients with chronic arm lymphoedema and tissue fibrosis after radiotherapy for early breast cancerLone Gothard, Anthony Stanton, Julie MacLaren, et al.European Journal of Human Genetics : EJHG|January 17, 2008
Primary non-syndromic lymphoedema (Meige disease) is not caused by mutations in FOXC2Tayebeh Rezaie, Rose Ghoroghchian, Rachel Bell, et al.The British Journal of Radiology|January 10, 2026
Indocyanine Green Lymphography Imaging of Normal Lymphatic Drainage in the Lower LimbsMike Mills, Malou van Zanten, Greta Brezgyte, et al.Human Genetics|May 21, 2005
Lymphoedema-distichiasis and FOXC2: unreported mutations, de novo mutation estimate, families without coding mutationsCarolyn Sholto-Douglas-Vernon, Rachel Bell, Glen Brice, et al.Pageof 5