A. Daly

发表

Genetic Causes of Familial Pituitary Adenomas

A. Beckers, S. Vandeva, S. Zacharieva, 2011 .

Genetic analysis in young patients with sporadic pituitary macroadenomas: besides AIP don't forget MEN1 genetic analysis.

A. Tabarin, V. Rohmer, P. Caron, 2013, European journal of endocrinology.

Cytokine Dysregulation, Inflammation and Well-Being

A. Harris, G. Chrousos, I. Elenkov, 2005, Neuroimmunomodulation.

Pancreatic Neuroendocrine Neoplasm Associated with a Familial MAX Deletion

E. Korpershoek, V. Bours, V. Dideberg, 2020, Hormone and Metabolic Research.

Serum levels of soluble CD163 correlate with the inflammatory process in coeliac disease

C. Feighery, A. Daly, C. Walsh, 2006, Alimentary pharmacology & therapeutics.

Germline AIP, MEN1, PRKAR1A, CDKN1B (p27Kip1) and CDKN2C (p18INK4c) gene mutations in a large cohort of pediatric patients with pituitary adenomas occurring in isolation or with associated syndromic features

V. Bours, C. Stratakis, A. Horvath, 2008 .

Diabètes secondaires a une endocrinopathie

A. Beckers, D. Betea, A. Daly, 2005 .

Oral vitamin C reduces the injury to skeletal muscle caused by compartment syndrome.

K. Sheehan, C. Kelly, A. Daly, 2004, The Journal of bone and joint surgery. British volume.

Oral vitamin C attenuates acute ischaemia-reperfusion injury in skeletal muscle.

C. Kelly, A. Daly, A. Daly, 2001, The Journal of bone and joint surgery. British volume.

GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone Deficiency

V. Bours, C. Stratakis, A. Barlier, 2016, Hormone and Metabolic Research.

Clinical and genetic aspects of familial isolated pituitary adenomas

L. Naves, A. Beckers, S. Zacharieva, 2012, Clinics.

Management of acromegaly

A. Beckers, S. Zacharieva, A. Daly, 2010, F1000 medicine reports.