Mutational analysis for biotinidase deficiency of a Greek patients' cohort ascertained through expanded newborn screening
Thodi, Georgia, Molou, Elina, Georgiou, Vassiliki, Loukas, Yannis L, Dotsikas, Yannis, Biti, Sofia, Papadopoulos, Konstantinos, Konstantinou, Dimitris, Antoniadi, Marina, Doulgerakis, Emmanuel
Published in Journal of human genetics (01.12.2011)
Published in Journal of human genetics (01.12.2011)
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Rhinovirus‐induced basic fibroblast growth factor release mediates airway remodeling features
Skevaki, Chrysanthi L, Psarras, Stelios, Volonaki, Eleni, Pratsinis, Harris, Spyridaki, Irini S, Gaga, Mina, Georgiou, Vassiliki, Vittorakis, Stylianos, Telcian, Aurica G, Maggina, Paraskevi, Kletsas, Dimitris, Gourgiotis, Dimitrios, Johnston, Sebastian L, Papadopoulos, Nikolaos G
Published in Clinical and translational allergy (21.08.2012)
Published in Clinical and translational allergy (21.08.2012)
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Determination of malathion, coumaphos, and fluvalinate residues in honey by gas chromatography with nitrogen-phosphorus or electron capture detectors
Menkissoglu-Spiroudi, U, Diamantidis, G C, Georgiou, V E, Thrasyvoulou, A T
Published in Journal of AOAC International (01.01.2000)
Published in Journal of AOAC International (01.01.2000)
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High incidence of partial biotinidase deficiency cases in newborns of Greek origin
Thodi, Georgia, Schulpis, Kleopatra H., Molou, Elina, Georgiou, Vassiliki, Loukas, Yannis L., Dotsikas, Yannis, Papadopoulos, Konstantinos, Biti, Sofia
Published in Gene (25.07.2013)
Published in Gene (25.07.2013)
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Clinical diagnostic Next-Generation sequencing: The case of CFTR carrier screening
Loukas, Yannis L., Thodi, Georgia, Molou, Elina, Georgiou, Vassiliki, Dotsikas, Yannis, Schulpis, Kleopatra H.
Published in Scandinavian journal of clinical and laboratory investigation (01.09.2015)
Published in Scandinavian journal of clinical and laboratory investigation (01.09.2015)
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Expanded newborn screening in Greece: 30 months of experience
Loukas, Yannis L., Soumelas, Georgios-Stefanos, Dotsikas, Yannis, Georgiou, Vassiliki, Molou, Elina, Thodi, Georgia, Boutsini, Maria, Biti, Sofia, Papadopoulos, Konstantinos
Published in Journal of inherited metabolic disease (01.12.2010)
Published in Journal of inherited metabolic disease (01.12.2010)
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Early screening of FTO and MC4R variants in newborns of Greek origin
Molou, Elina, Schulpis, Kleopatra H., Birbilis, Christos, Thodi, Georgia, Georgiou, Vassiliki, Dotsikas, Yannis, Loukas, Yannis L.
Published in Journal of Pediatric Endocrinology & Metabolism (01.05.2015)
Published in Journal of Pediatric Endocrinology & Metabolism (01.05.2015)
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Characterization of the molecular spectrum of Medium-Chain Acyl-CoA Dehydrogenase Deficiency in a Greek newborns cohort: Identification of a novel variant
Thodi, Georgia, Georgiou, Vassiliki, Molou, Elina, Loukas, Yannis L., Dotsikas, Yannis, Biti, Sofia, Papadopoulos, Konstantinos, Doulgerakis, Emmanuel
Published in Clinical biochemistry (01.10.2012)
Published in Clinical biochemistry (01.10.2012)
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Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency in Greek newborns: The Mediterranean C563T mutation screening
Molou, Elina, Schulpis, Kleopatra H., Thodi, Georgia, Georgiou, Vassiliki, Dotsikas, Yannis, Papadopoulos, Konstantinos, Biti, Sofia, Loukas, Yannis L.
Published in Scandinavian journal of clinical and laboratory investigation (01.04.2014)
Published in Scandinavian journal of clinical and laboratory investigation (01.04.2014)
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Erratum to: Expanded newborn screening in Greece: 30 months of experience
Loukas, Yannis L., Soumelas, Georgios-Stefanos, Dotsikas, Yannis, Georgiou, Vassiliki, Molou, Elina, Thodi, Georgia, Boutsini, Maria, Biti, Sofia, Papadopoulos, Konstantinos
Published in Journal of inherited metabolic disease (01.07.2013)
Published in Journal of inherited metabolic disease (01.07.2013)
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