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Psychoneuroendocrinology|January 1, 1991
Cortisol escape from suppression by dexamethasone during depression is strongly predicted by basal cortisol hypersecretion and increasing age combinedM Maes, B Minner, E Suy, et al.
Biological Psychiatry|April 15, 1994
Lower serum prolyl endopeptidase enzyme activity in major depression: further evidence that peptidases play a role in the pathophysiology of depressionM Maes, F Goossens, S Scharpé, et al.
Revue De Stomatologie Et De Chirurgie Maxillo-Faciale|December 19, 2002
[Retrospective study of two years of surgery for temporomandibular joint pain dysfunction syndrome]E Lemière, J M Maes, D Rousie, et al.
Psychological Medicine|August 13, 2002
Platelet alpha2-adrenoceptor density in humans: relationships to stress-induced anxiety, psychasthenic constitution, gender and stress-induced changes in the inflammatory response systemM Maes, A Van Gastel, L Delmeire, et al.
The Journal of Biological Chemistry|July 20, 2004
Structural dynamics controls nitric oxide affinity in nitrophorin 4Karin Nienhaus, Estelle M Maes, Andrzej Weichsel, et al.
Psychological Medicine|April 22, 2005
Early increase in vegetative symptoms predicts IFN-alpha-induced cognitive-depressive changesM C Wichers, G H Koek, G Robaeys, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|January 16, 2021
Cytokine dependent hematopoietic cell linker (CLNK) is highly elevated in blood transfusion dependent beta-thalassemia major patientsH K Al-Hakeim, H H Al-Mayali, S R Moustafa, et al.
Hormone Research|January 1, 1997
Factors determining pubertal growth and final height in growth hormone treatment of idiopathic growth hormone deficiency. Analysis of 195 Patients of the Kabi Pharmacia International Growth StudyM B Ranke, D A Price, K Albertsson-Wikland, et al.
American Journal of Diseases of Children (1960)|May 1, 1980
Phenotypic variation in a family with partial androgen insensitivity syndromeM Maes, P A Lee, R D Jeffs, et al.
European Journal of Endocrinology|September 26, 2007
Clinical and biological phenotype of a patient with familial glucocorticoid deficiency type 2 caused by a mutation of melanocortin 2 receptor accessory proteinH Rumié, L A Metherell, A J L Clark, et al.
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