Triana, P., Dore, M., Cerezo, V. N. N. N., Cervantes, M., Sánchez, A. V. A. V., Ferrero, M. M. M. M., … Lopez-Gutierrez, J. C. J. C. (2017). Sirolimus in the Treatment of Vascular Anomalies. European Journal of Pediatric Surgery27(1), 086–090.

Ludwig, K. F., Slone, T., Cederberg, K. B., Silva, A. T., & Dellinger, M. T. (2016). A new case and review of chylothorax in generalized lymphatic anomaly and gorham-stout disease. Lymphology49(2).

Nadal, M., Giraudeau, B., Tavernier, E., Jonville-Bera, A., Lorette, G., & Maruani, A. (2016). Efficacy and Safety of Mammalian Target of Rapamycin Inhibitors in Vascular Anomalies: A Systematic Review. Acta Dermato Venereologica96(4), 448–452.

Ozeki, M., Fujino, A., Matsuoka, K., Nosaka, S., Kuroda, T., & Fukao, T. (2016). Clinical Features and Prognosis of Generalized Lymphatic Anomaly, Kaposiform Lymphangiomatosis, and Gorham-Stout Disease. Pediatric Blood and Cancer63(5), 832–838.

Goyal, P., Alomari, A. I. A. I., Kozakewich, H. P. H. P., Trenor, C. C. C., Perez-Atayde, A. R. A. R. A. R. A. R. A. R., Fishman, S. J. S. J., … Chaudry, G. (2016). Imaging features of kaposiform lymphangiomatosis. Pediatric Radiology46(9), 1282–1290.

Herruela-Suffee, C., Warin, M., Castier-Amouyel, M., Dallery, F., Bonnaire, B., & Constans, J.-M. J. M. (2016). Whole-body MRI in generalized cystic lymphangiomatosis in the pediatric population: diagnosis, differential diagnoses, and follow-up. Skeletal Radiology45(2), 177–185.

Liu, Y. Y., Zhong, D. R. D.-R., Zhou, P. R. P.-R. P. R., Lv, F., Ma, D. D. D.-D., Xia, W.-B. W. B., … Li, M. (2016). Gorham-Stout disease: radiological, histological, and clinical features of 12 cases and review of literature. Clinical Rheumatology35(3), 813–823.

Adams, D. M., Trenor, C. C., Hammill, A. M., Vinks, A. A., Patel, M. N., Chaudry, G., … Azizkhan, R. G. (2016). Efficacy and Safety of Sirolimus in the Treatment of Complicated Vascular Anomalies. Pediatrics137(2), e20153257–e20153257.

Luisi, F., Torre, O., & Harari, S. (2016). Thoracic involvement in generalised lymphatic anomaly (or lymphangiomatosis). European Respiratory Review25(140), 170–177.

Iacobas, I., Klepper, L., Kelly, J., Ferry, T., & Dellinger, M. T. (2016). Meeting Report for the 2016 Conference on GLA and Gorham–Stout Disease. IBMS BoneKEy13, 847.

Mori, M., Dictor, M., Brodszki, N., López-Gutiérrez, J. C., Beato, M., Erjefält, J. S., & Eklund, E. A. (2016). Pulmonary and pleural lymphatic endothelial cells from pediatric, but not adult, patients with Gorham-Stout disease and generalized lymphatic anomaly, show a high proliferation rate. Orphanet Journal of Rare Diseases11(1).

Kato, H., Ozeki, M., Fukao, T., & Matsuo, M. (2016). Craniofacial CT findings of Gorham–Stout disease and generalized lymphatic anomaly. Neuroradiology58(8), 801–806.

Wassef, M., Blei, F., Adams, D., Alomari, A., & Baselga, E. (2015). Vascular Anomalies Classi fi cation: Recommendations From the International Society for the Study of Vascular Anomalies136(1).