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Journal of Clinical Research in Pediatric Endocrinology|April 19, 2016
Identification and Functional Characterization of a Calcium-Sensing Receptor Mutation in an Infant with Familial Hypocalciuric HypercalcemiaAnna Papadopoulou, Evangelia Gole, Katerina Melachroinou, et al.
Acta Paediatrica (Oslo, Norway : 1992)|May 8, 2008
Age at menarche in contemporary Greek girls: evidence for levelling-off of the secular trendAnastasios Papadimitriou, Grigorios Fytanidis, Konstandinos Douros, et al.
Endocrine-Related Cancer|February 19, 2025
Local treatments and TKI efficacy in radioiodine refractory differentiated thyroid carcinoma patients: a single center experienceKaterina Saltiki, Olga Karapanou, Kanella Kantreva, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine|September 24, 2011
Pubertal maturation of contemporary Greek boys: no evidence of a secular trendAnastasios Papadimitriou, Konstantinos Douros, Kleanthis Kleanthous, et al.
The Journal of Clinical Endocrinology and Metabolism|August 30, 2008
Timing of pubertal onset in girls: evidence for non-Gaussian distributionAnastasios Papadimitriou, Soula Pantsiotou, Konstandinos Douros, et al.
Neuroimmunomodulation|July 3, 2009
Endocrine-immune interactions in adrenal function of asthmatic children on inhaled corticosteroidsKostas N Priftis, Anastasios Papadimitriou, Michael B Anthracopoulos, et al.
BMC Public Health|July 6, 2007
Aims, methods and preliminary findings of the Physical Activity, Nutrition and Allergies in Children Examined in Athens (PANACEA) epidemiological studyKostas N Priftis, Demosthenes B Panagiotakos, Michael B Anthracopoulos, et al.
Pediatrics|January 2, 2008
A novel monocarboxylate transporter 8 gene mutation as a cause of severe neonatal hypotonia and developmental delayAnastasios Papadimitriou, Alexandra Mihaela Dumitrescu, Antigone Papavasiliou, et al.
Acta Paediatrica (Oslo, Norway : 1992)|May 15, 2008
Greek young men grow tallerAnastasios Papadimitriou, Grigorios Fytanidis, Konstandinos Douros, et al.
Pediatric Research|November 20, 2002
Low TSH congenital hypothyroidism: identification of a novel mutation of the TSH beta-subunit gene in one sporadic case (C85R) and of mutation Q49stop in two siblings with congenital hypothyroidismAmalia Sertedaki, Anastasios Papadimitriou, Antony Voutetakis, et al.
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