Zobrazeno 1 - 10
of 214
pro vyhledávání: '"Thodi, G."'
Autor:
Thodi G; Neoscreen Diagnostic Laboratory, Athens, Greece., Triantopoulou A; Laboratory of Pharmaceutical Analysis, Department of Pharmacy, National and Kapodistrian University of Athens, Athens, Greece., Iliou A; Laboratory of Pharmaceutical Analysis, Department of Pharmacy, National and Kapodistrian University of Athens, Athens, Greece., Molou E; Neoscreen Diagnostic Laboratory, Athens, Greece., Dotsikas Y; Laboratory of Pharmaceutical Analysis, Department of Pharmacy, National and Kapodistrian University of Athens, Athens, Greece., Loukas YL; Laboratory of Pharmaceutical Analysis, Department of Pharmacy, National and Kapodistrian University of Athens, Athens, Greece.
Publikováno v:
Scandinavian journal of clinical and laboratory investigation [Scand J Clin Lab Invest] 2024 Sep; Vol. 84 (5), pp. 326-335. Date of Electronic Publication: 2024 Sep 03.
Autor:
Rădoi VE; Department of Medical Genetics, 'Carol Davila' University of Medicine and Pharmacy, 020021 Bucharest, Romania.; 'Alessandrescu-Rusescu' National Institute for Maternal and Child Health, 20382 Bucharest, Romania.; Personal Genetics, 010987 Bucharest, Romania.; Sanador, 011026 Bucharest, Romania., Țurcan M; Department of Medical Genetics, 'Carol Davila' University of Medicine and Pharmacy, 020021 Bucharest, Romania.; Personal Genetics, 010987 Bucharest, Romania., Maioru OV; Department of Medical Genetics, 'Carol Davila' University of Medicine and Pharmacy, 020021 Bucharest, Romania., Dan A; Department of Medical Genetics, 'Carol Davila' University of Medicine and Pharmacy, 020021 Bucharest, Romania., Bohîlțea LC; Department of Medical Genetics, 'Carol Davila' University of Medicine and Pharmacy, 020021 Bucharest, Romania.; 'Alessandrescu-Rusescu' National Institute for Maternal and Child Health, 20382 Bucharest, Romania., Dumitrescu EA; Department of Oncology, 'Carol Davila' University of Medicine and Pharmacy, 020021 Bucharest, Romania., Gheorghe AS; Department of Oncology, 'Carol Davila' University of Medicine and Pharmacy, 020021 Bucharest, Romania.; Department of Medical Oncology I, Institute of Oncology 'Prof. Dr. Al. Trestioreanu' Bucharest, 022328 Bucharest, Romania., Stănculeanu DL; Department of Oncology, 'Carol Davila' University of Medicine and Pharmacy, 020021 Bucharest, Romania.; Department of Medical Oncology I, Institute of Oncology 'Prof. Dr. Al. Trestioreanu' Bucharest, 022328 Bucharest, Romania., Thodi G; Neoscreen Diagnostic Laboratory, Voreiou Ipeirou, 15235 Athens, Greece., Loukas YL; School of Pharmacy, University of Athens, Panepistimiolopis, 15771 Zografou, Greece., Săbău ID; Department of Medical Genetics, 'Carol Davila' University of Medicine and Pharmacy, 020021 Bucharest, Romania.; Personal Genetics, 010987 Bucharest, Romania.
Publikováno v:
Diagnostics (Basel, Switzerland) [Diagnostics (Basel)] 2023 May 29; Vol. 13 (11). Date of Electronic Publication: 2023 May 29.
Autor:
Schulpis KH; Institute of Child Health, Aghia Sophia Children's Hospital, Athens, Greece., Thodi G; Laboratory of Prenatal and Neonatal Screening, Neoscreen Ltd., Athens, Greece., Iakovou K; Institute of Child Health, Aghia Sophia Children's Hospital, Athens, Greece., Dotsikas Y; Laboratory of Pharm. Analysis, Department of Pharmacy, National and Kapodestrian University of Athens, Athens, Greece., Molou E; Laboratory of Prenatal and Neonatal Screening, Neoscreen Ltd., Athens, Greece., Loukas YL; Laboratory of Pharm. Analysis, Department of Pharmacy, National and Kapodestrian University of Athens, Panepistimiopolis Zographou, 157 71, Athens, Greece, Phone: +30 210 7274224, Fax: +30 211 1826131.
Publikováno v:
Journal of pediatric endocrinology & metabolism : JPEM [J Pediatr Endocrinol Metab] 2018 Jan 26; Vol. 31 (2), pp. 221-222.
A fully automated liquid chromatography-tandem mass spectrometry (LC–MS/MS) method was developed for the determination of omeprazole in human plasma. Utilization of 96-well plates and robotic liquid handling workstations, rendered the whole procedu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::edbd6777d4574e25925042bbdba201b7
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3026266
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3026266
Classical galactosaemia is an inborn error of metabolism due to the deficiency of the enzyme galactose-1-phosphate uridylyltransferase (GALT). The aim of the study was to identify the underlying mutations in Greek patients with GALT deficiency and ev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::f6f09093274e9cdbe6b356190030d2a4
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3086743
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3086743
Background: Deficiencies of galactokinase (GALK) and UDP-epimerase (GALE) are implicated with galactose metabolic disorders. The aim of the study was the identification of mutations in GALK and GALE genes and clinical evaluation of patients. Methods:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::bb056bcd75432eb8b1825589ba02ad5b
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3086908
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3086908
Autor:
Schulpis KH; Institute of Child Health, Aghia Sophia Children's Hospital, Athens, Greece., Molou E; Laboratory of Prenatal and Neonatal Screening, Neoscreen Ltd., Athens, Greece., Manta-Vogli P; Department of Clinical Nutrition and Dietetics, Aghia Sofia Children's Hospital, Athens, Greece., Dotsikas Y; Laboratory of Pharmaceutical Analysis, Department of Pharmacy, National and Kapodistrian University of Athens, Athens, Greece., Thodi G; Laboratory of Prenatal and Neonatal Screening, Neoscreen Ltd., Athens, Greece., Chatzidaki M; Laboratory of Prenatal and Neonatal Screening, Neoscreen Ltd., Athens, Greece., Loukas YL; Laboratory of Pharmaceutical Analysis, Department of Pharmacy, National and Kapodistrian University of Athens, Athens, Greece.
Publikováno v:
American journal of perinatology [Am J Perinatol] 2021 Jul; Vol. 38 (8), pp. 828-833. Date of Electronic Publication: 2019 Dec 31.
Background: Hawkinsinuria is a rare inborn error of tyrosine metabolism. Objectives: To study novel hawkinsinuria cases by monitoring their biochemical profile and conducting a mutation analysis. Subjects and methods: Among 92,519 newborns that under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::22b02602b6099557721c82658c6426f6
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3086850
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3086850