A. Mendola

发表

Isolated bilateral transverse agenesis of the distal segments of the lower limbs at the level of the knee joint in a human fetus

Y. Gillerot, M. Vikkula, C. Godfraind, 2016, American journal of medical genetics. Part A.

Blue Rubber Bleb Nevus (BRBN) Syndrome Is Caused by Somatic TEK (TIE2) Mutations.

J. Mulliken, R. Helaers, M. Vikkula, 2017, The Journal of investigative dermatology.

Somatic Activating PIK3CA Mutations Cause Venous Malformation.

R. Helaers, M. Vikkula, C. Godfraind, 2015, American journal of human genetics.

Venous malformation-causative TIE2 mutations mediate an AKT-dependent decrease in PDGFB.

M. Vikkula, C. Godfraind, L. Eklund, 2013, Human molecular genetics.

Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas.

S. Gruber, C. Ricketts, M. Vikkula, 2010, JAMA.

Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 Mutations

R. Hennekam, D. Lev, M. Vikkula, 2012, Molecular Syndromology.

Rapamycin improves TIE 2-mutated venous malformation in murine model and human subjects

E. Boscolo, M. Vikkula, C. Legrand, 2015 .

RASA1 Mutations and Associated Phenotypes in 68 Families with Capillary Malformation–Arteriovenous Malformation

W. Chung, C. Cytrynbaum, N. Brunetti‐Pierri, 2013, Human mutation.

No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome

T. de Ravel, K. Devriendt, H. Van Esch, 2015, Orphanet Journal of Rare Diseases.

Mutations in the VEGFR3 Signaling Pathway Explain 36% of Familial Lymphedema

A. Irrthum, J. Mulliken, M. Vikkula, 2013, Molecular Syndromology.

STK39 and WNK1 Are Potential Hypertension Susceptibility Genes in the BELHYPGEN Cohort

J. Staessen, M. Vikkula, S. Horman, 2016, Medicine.

Rapamycin improves TIE2-mutated venous malformation in murine model and human subjects.

E. Boscolo, M. Vikkula, C. Legrand, 2015, The Journal of clinical investigation.

Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy.

M. Simpson, M. Vikkula, R. Trembath, 2012, American journal of human genetics.

Prevalence and Spectrum of SDHx Mutations in Pheochromocytoma and Paraganglioma in Patients from Belgium: An Update

M. Vikkula, M. Hamoir, D. Maiter, 2012, Hormone and Metabolic Research.

Liquid biopsy for mutational profiling of locoregional recurrent and/or metastatic head and neck squamous cell carcinoma.

J. Machiels, R. Helaers, M. Vikkula, 2020, Oral oncology.

Preclinical Evaluation of the Association of the Cyclin-Dependent Kinase 4/6 Inhibitor, Ribociclib, and Cetuximab in Squamous Cell Carcinoma of the Head and Neck

D. Vertommen, J. Machiels, P. Roger, 2021, Cancers.