Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Ioannis, Monopolis"'
Autor:
Artemis Doulgeraki, Vasiliki Schiza, Kalliopi Drakaki, Jacqueline Yousef, Helen Athanasopoulou, Christine Fragodimitri, Fotis Karabatsos, Ioannis Monopolis, Antonia Chatziliami
Publikováno v:
Hemoglobin. 45(1)
Hereditary hemolytic disorders cause ineffective erythropoiesis and bone marrow hyperplasia. Little is known about their effect on growth and skeletal health. The aim of this study was to evaluate growth, bone and body composition of non transfusion-
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEMReferences. 32(3)
Background Phenylketonuria (PKU) is an inherited metabolic disorder characterized by high levels of phenylalanine in the blood and brain, resulting in mental retardation, etc. Dietary treatment with low phenylalanine is the common treatment for this
Publikováno v:
Bone Abstracts.
Autor:
Ioannis Monopolis, Vassiliki Kitra, K Kaisari, Elpis Vlachopapadopoulou, G Vessalas, Artemis Doulgeraki, Ioulia Peristeri, Stefanos Michalacos, G. Polizois, Anna Paisiou
Publikováno v:
Bone Abstracts.
Publikováno v:
Minerva pediatrica. 68(6)
Autor:
Helen Michelakakis, Leonidas Stefanis, Nick Dekker, Georgia Dermentzaki, Ioannis Monopolis, Marina Moraitou, E. Dimitriou, Hans Aerts
Publikováno v:
Neuroscience letters, 613, 1-5. Elsevier Ireland Ltd
Several observations suggest that disturbed homeostasis of α-Synuclein (α-Syn) may provide a link between Gaucher disease (GD) and Parkinson's disease (PD). We recently reported increased dimerization of α-Syn in the red blood cell (RBC) membrane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c076209d0f6f2ed72d3de06b519525e
https://hdl.handle.net/1887/3199778
https://hdl.handle.net/1887/3199778
Autor:
Ioanna Paspati, Glykeria Petrocheilou, Helen Athanasopoulou, Marina Katsalouli, Artemis Doulgeraki, Ioannis Monopolis
Publikováno v:
Acta neurologica Belgica. 116(4)
Greece ranks among the first countries suffering from the obesity epidemic globally. The aim of the study was to evaluate body composition in Greek patients with Duchenne muscular dystrophy (DMD). We hypothesized that able-bodied patients would not d
Autor:
Glykeria Petrocheilou, Ioanna Paspati, Ioannis Monopolis, Helen Athanasopoulou, Artemis Doulgeraki, Marina Katsalouli
Publikováno v:
Bone Abstracts.
Autor:
Argyri Petrocheilou, Athanasios G. Kaditis, Artemis Doulgeraki, S. Doudounakis, Glykeria Petrocheilou, George P. Chrousos, Ioannis Monopolis
Publikováno v:
Bone Abstracts.
Autor:
Artemis Doulgeraki, Astrinia Skarpalezou, Ioannis Monopolis, Areti Theodosiadou, Kleopatra H. Schulpis
Publikováno v:
International Journal of Endocrinology and Metabolism
Background: There is evidence in support of low bone density in young patients with disorders of phenylalanine metabolism; however, little is known about muscle and fat mass in these patients, especially in those with mild hyperphenylalaninemia (mHPA