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DELANNOY Pauline

Département de médecine interne > Service d'endocrinologie clinique

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Main Referenced Co-authors
Beckers, Albert  (7)
Valdes-Socin, Hernan  (5)
Cavalier, Etienne  (2)
Debray, François-Guillaume  (2)
Potorac, Iulia  (2)
Main Referenced Keywords
PTEN (2); active B12 (1); b12 (1); Biermer disease (1); Classification (1);
Main Referenced Disciplines
Endocrinology, metabolism & nutrition (7)
Oncology (1)
Genetics & genetic processes (1)

Publications (total 8)

The most downloaded
1188 downloads
DELANNOY, P., VRANKEN, L., CAVALIER, E., & VALDES SOCIN, H. G. (2020). Carence en vitamine B12 : diagnostic et prise en charge. Tempo Médical, 24-28. https://hdl.handle.net/2268/252550

The most cited

5 citations (OpenCitations)

DELANNOY, P., Debray, F.-G., Verloes, A., Beckers, A., & VALDES SOCIN, H. G. (2017). How to recognize Cowden syndrome: A novel PTEN mutation description. Annales d'Endocrinologie. doi:10.1016/j.ando.2017.01.001 https://hdl.handle.net/2268/219076

DELANNOY, P., NECHIFOR - POTORAC, I., & Beckers, A. (2022). Nouveautés dans le diagnostic et la prise en charge des complications en lien avec l'acromégalie. Vaisseaux, Coeur, Poumons, 27 (3), 14-20.
Peer reviewed

Lousberg, L., Collignon, J., Troisfontaine, F., PAULUS, A., VAILLANT, F., DELANNOY, P., Petignot, S., Petrossians, P., Rohmer, V., Jadoul, A., & Beckers, A. (2021). Néoplasies neuroendocrines : une nouvelle ère a l’apogée de la multidisciplinarité ! Revue Médicale de Liège, 76 (5-6), 425-431.
Editorial Reviewed verified by ORBi

DELANNOY, P., NECHIFOR - POTORAC, I., & Beckers, A. (2021). Multiple Endocrine Neoplasia Type 1 in Clinical Practice. In Endocrinology. Springer International Publishing. doi:10.1007/978-3-319-89497-3_19
Peer reviewed

DELANNOY, P., VRANKEN, L., CAVALIER, E., & VALDES SOCIN, H. G. (2020). Carence en vitamine B12 : diagnostic et prise en charge. Tempo Médical, 24-28.

DELANNOY, P., GRANDFILS, S., LEBRETHON, M.-C., CHANTRAINE, F., VAN LINTHOUT, C., BECKERS, A., & VALDES SOCIN, H. G. (2019). A series of 9 pregnancies with hyperthyroidism and Graves disease : fetal and maternal follow up. In Abstract book : Annual congress of the Belgian Society of Internal Medicine.

VALDES SOCIN, H. G., VRANKEN, L., Schoneveld, L., DELANNOY, P., Le Goff, C., Beckers, A., & CAVALIER, E. (2019). Vitamin B12 deficiency prevalence and associated biomarkers in type 2 Diabetes (T2DM) treated with metformin : biochemical assessment in a series of 106 patients. In Endocrine Abstracts - ECE 2019.

DELANNOY, P., Debray, F.-G., Verloes, A., Beckers, A., & VALDES SOCIN, H. G. (2017). How to recognize Cowden syndrome: A novel PTEN mutation description. Annales d'Endocrinologie. doi:10.1016/j.ando.2017.01.001
Peer Reviewed verified by ORBi

DELANNOY, P., DEBRAY, F.-G., BECKERS, A., & VALDES SOCIN, H. G. (2014). Cowden Syndrome: a novel PTEN mutation description and how to recognize a not so rare hereditary cancer syndrome. Acta Clinica Belgica, 69 (suppl 3), 16.
Peer Reviewed verified by ORBi

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