H. Du Boullay

Long-term Follow-up of MEN1 Patients Who Do Not Have Initial Surgery for Small ≤2 cm Nonfunctioning Pancreatic Neuroendocrine Tumors, an AFCE and GTE Study

E. Baudin, F. Pattou, P. Chaffanjon, 2017, Annals of surgery.

A comparative phenotypic study of kallmann syndrome patients carrying monoallelic and biallelic mutations in the prokineticin 2 or prokineticin receptor 2 genes.

P. Tonella, B. Conrad, J. Hardelin, 2010, The Journal of clinical endocrinology and metabolism.

MEN1 disease occurring before 21 years old: a 160-patient cohort study from the Groupe d'étude des Tumeurs Endocrines.

A. Tabarin, X. Bertagna, P. Ruszniewski, 2015, The Journal of clinical endocrinology and metabolism.

Gender-related differences in MEN1 lesion occurrence and diagnosis: a cohort study of 734 cases from the Groupe d'etude des Tumeurs Endocrines.

A. Tabarin, P. Caron, P. Ruszniewski, 2011, European journal of endocrinology.

Unraveling the intrafamilial correlations and heritability of tumor types in MEN1: a Groupe d'étude des Tumeurs Endocrines study.

P. Chanson, A. Tabarin, E. Baudin, 2015, European journal of endocrinology.

Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d'etude des Tumeurs Endocrines (GTE) cohort study.

P. Chanson, A. Tabarin, E. Baudin, 2013, Human molecular genetics.

Adrenal involvement in MEN1. Analysis of 715 cases from the Groupe d'etude des Tumeurs Endocrines database.

A. Tabarin, E. Baudin, Jacques Young, 2012, European journal of endocrinology.

Pituitary MRI Features in Acromegaly due to Ectopic GHRH Secretion from a Neuroendocrine Tumor: Analysis of 30 cases.

P. Chanson, L. Tshibanda, M. Korbonits, 2022, The Journal of clinical endocrinology and metabolism.