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Georgia Thodi

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Scandinavian Journal of Clinical and Laboratory Investigation|June 24, 2017
Mutational analysis of GALT gene in Greek patients with galactosaemia: identification of two novel mutations and clinical evaluationKleopatra H Schulpis, Georgia Thodi, Konstantinos Iakovou, et al.
Gene|May 7, 2013
High incidence of partial biotinidase deficiency cases in newborns of Greek originGeorgia Thodi, Kleopatra H Schulpis, Elina Molou, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 5, 2017
Clinical evaluation and mutational analysis of GALK and GALE genes in patients with galactosemia in Greece: one novel mutation and two rare casesKleopatra H Schulpis, Georgia Thodi, Konstantinos Iakovou, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|January 28, 2014
Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency in Greek newborns: the Mediterranean C563T mutation screeningElina Molou, Kleopatra H Schulpis, Georgia Thodi, et al.
Journal of Inherited Metabolic Disease|August 20, 2010
Expanded newborn screening in Greece: 30 months of experienceYannis L Loukas, Georgios-Stefanos Soumelas, Yannis Dotsikas, et al.
Journal of Human Genetics|October 21, 2011
Mutational analysis for biotinidase deficiency of a Greek patients' cohort ascertained through expanded newborn screeningGeorgia Thodi, Elina Molou, Vassiliki Georgiou, et al.
BMC Cancer|October 13, 2010
Screening of the DNA mismatch repair genes MLH1, MSH2 and MSH6 in a Greek cohort of Lynch syndrome suspected familiesGeorgia Thodi, Florentia Fostira, Raphael Sandaltzopoulos, et al.
Diagnostics (Basel, Switzerland)|June 10, 2023
Homologous Recombination Deficiency Score Determined by Genomic Instability in a Romanian CohortViorica-Elena Rădoi, Mihaela Țurcan, Ovidiu Virgil Maioru, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Scandinavian Journal of Clinical and Laboratory Investigation|June 24, 2017
Mutational analysis of GALT gene in Greek patients with galactosaemia: identification of two novel mutations and clinical evaluationKleopatra H Schulpis, Georgia Thodi, Konstantinos Iakovou, et al.
Gene|May 7, 2013
High incidence of partial biotinidase deficiency cases in newborns of Greek originGeorgia Thodi, Kleopatra H Schulpis, Elina Molou, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 5, 2017
Clinical evaluation and mutational analysis of GALK and GALE genes in patients with galactosemia in Greece: one novel mutation and two rare casesKleopatra H Schulpis, Georgia Thodi, Konstantinos Iakovou, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|January 28, 2014
Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency in Greek newborns: the Mediterranean C563T mutation screeningElina Molou, Kleopatra H Schulpis, Georgia Thodi, et al.
Journal of Inherited Metabolic Disease|August 20, 2010
Expanded newborn screening in Greece: 30 months of experienceYannis L Loukas, Georgios-Stefanos Soumelas, Yannis Dotsikas, et al.
Journal of Human Genetics|October 21, 2011
Mutational analysis for biotinidase deficiency of a Greek patients' cohort ascertained through expanded newborn screeningGeorgia Thodi, Elina Molou, Vassiliki Georgiou, et al.
BMC Cancer|October 13, 2010
Screening of the DNA mismatch repair genes MLH1, MSH2 and MSH6 in a Greek cohort of Lynch syndrome suspected familiesGeorgia Thodi, Florentia Fostira, Raphael Sandaltzopoulos, et al.
Diagnostics (Basel, Switzerland)|June 10, 2023
Homologous Recombination Deficiency Score Determined by Genomic Instability in a Romanian CohortViorica-Elena Rădoi, Mihaela Țurcan, Ovidiu Virgil Maioru, et al.
Pageof 2