Elina Molou

Athens, ESYE31 15235, Greece

Last Updated: 09/26/2026

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Found 16 publications

Rare-ID: Genomic Diagnosis in Symptomatic Neonates and Young Infants with Complex Clinical Phenotypes: A Descriptive Cohort Study.

Rare-ID: Genomic Diagnosis in Symptomatic Neonates and Young Infants with Complex Clinical Phenotypes: A Descriptive Cohort Study.

Journal: Genes

Published: May 19, 2026

A simplified metabolomic analysis of dried blood spots in breast cancer patients.

A simplified metabolomic analysis of dried blood spots in breast cancer patients.

Journal: Scandinavian journal of clinical and laboratory investigation

Published: September 03, 2024

Perinatal Reduced Blood Concentrations of Free Carnitine and Acylcarnitines in Infants with Cystic Fibrosis.

Perinatal Reduced Blood Concentrations of Free Carnitine and Acylcarnitines in Infants with Cystic Fibrosis.

Journal: American journal of perinatology

Published: January 01, 2020

Identification of five mutations in a patient with galactose metabolic disorders.

Identification of five mutations in a patient with galactose metabolic disorders.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: October 24, 2017

Rare cases of galactose metabolic disorders: identification of more than two mutations per patient.

Rare cases of galactose metabolic disorders: identification of more than two mutations per patient.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: July 05, 2017

Mutational analysis of GALT gene in Greek patients with galactosaemia: identification of two novel mutations and clinical evaluation.

Mutational analysis of GALT gene in Greek patients with galactosaemia: identification of two novel mutations and clinical evaluation.

Journal: Scandinavian journal of clinical and laboratory investigation

Published: June 24, 2017

Clinical evaluation and mutational analysis of GALK and GALE genes in patients with galactosemia in Greece: one novel mutation and two rare cases.

Clinical evaluation and mutational analysis of GALK and GALE genes in patients with galactosemia in Greece: one novel mutation and two rare cases.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: February 10, 2017

Study of the effect of CYP2C19 polymorphisms on omeprazole pharmacokinetics by utilizing validated LC-MS/MS and Real Time-PCR methods.

Study of the effect of CYP2C19 polymorphisms on omeprazole pharmacokinetics by utilizing validated LC-MS/MS and Real Time-PCR methods.

Journal: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences

Published: January 12, 2016

Partial biotinidase deficiency: identification of a single novel mutation (p.H314R) in a Greek newborn.

Partial biotinidase deficiency: identification of a single novel mutation (p.H314R) in a Greek newborn.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: September 28, 2015

Clinical diagnostic Next-Generation sequencing: the case of CFTR carrier screening.

Clinical diagnostic Next-Generation sequencing: the case of CFTR carrier screening.

Journal: Scandinavian journal of clinical and laboratory investigation

Published: April 16, 2015

Hawkinsinuria in two unrelated Greek newborns: identification of a novel variant, biochemical findings and treatment.

Hawkinsinuria in two unrelated Greek newborns: identification of a novel variant, biochemical findings and treatment.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: March 25, 2015

Early screening of FTO and MC4R variants in newborns of Greek origin.

Early screening of FTO and MC4R variants in newborns of Greek origin.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: July 29, 2014

Showing 1-12 of 16

Last Updated: 09/26/2026