Emmanouil Manolakos
Athens, ESYE31 11528, Greece
Last Updated: 09/26/2026
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Found 62 publications
Abstracts of the 36th World Congress on Ultrasound in Obstetrics and Gynecology, 4-7 September 2026, London, UK.
Journal: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Published: July 06, 2026
The significance of ophthalmological evaluation in the correct diagnosis of pediatric insulin-dependent diabetes mellitus: lessons from novel WFS1 variants.
Journal: Diabetes & metabolism
Published: May 18, 2025
Prenatal Diagnosis of Bartter Syndrome: Lessons From a Complex Diagnostic Procedure.
Journal: Clinical case reports
Published: January 15, 2025
Association of Waardenburg syndrome with a new mutation in the PAX3 gene: A case report and literature review.
Journal: Biomedical reports
Published: November 10, 2024
Prenatal diagnosis of clinodactyly and its association with genetic syndromes: A case report.
Journal: Case reports in women's health
Published: October 21, 2024
Novel familial KDF1 mutation detected in members of a three-generation family with clinical manifestations of ectodermal dysplasia: A report of four cases.
Journal: Biomedical reports
Published: July 15, 2024
Prenatal diagnosis of 18p deletion and 8p trisomy syndrome: literature review and report of a novel case.
Journal: BMC women's health
Published: October 02, 2023
An asymptomatic male individual carrying a 5.72 Mb de novo deletion in 8p23.2‑p23.3: A case report.
Journal: Experimental and therapeutic medicine
Published: May 26, 2023
The Effect of Resolution Level and Targeted Design in the Diagnostic Performance of Prenatal Chromosomal Microarray Analysis.
Journal: Fetal diagnosis and therapy
Published: November 04, 2022
Prenatal Identification of a Novel Mutation in the MCPH1 Gene Associated with Autosomal Recessive Primary Microcephaly (MCPH) Using Next Generation Sequencing (NGS): A Case Report and Review of the Literature.
Journal: Children (Basel, Switzerland)
Published: August 25, 2022
Growth Hormone Deficiency due to p.(Gln467Argfs*64) Mutation in the ARID1B Gene in a Girl with Coffin-Siris Syndrome.
Journal: Molecular syndromology
Published: February 23, 2021
Last Updated: 09/26/2026