Ioannis Papoulidis

Thessaloniki, ESYE12, Greece

Last Updated: 09/26/2026

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Found 55 publications

Abstracts of the 36th World Congress on Ultrasound in Obstetrics and Gynecology, 4-7 September 2026, London, UK.

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

Abstracts of the 36th World Congress on Ultrasound in Obstetrics and Gynecology, 4-7 September 2026, London, UK.

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

Clinical and Molecular Study of a Gorlin Syndrome Type 1 Case.

Clinical and Molecular Study of a Gorlin Syndrome Type 1 Case.

Journal: Advances in experimental medicine and biology

Published: November 22, 2025

The Novel ACTC1 p.Gly50Ser Variant Is Associated With Arrhythmia and Secondary Features of HCM Without Hypertrophy.

The Novel ACTC1 p.Gly50Ser Variant Is Associated With Arrhythmia and Secondary Features of HCM Without Hypertrophy.

Journal: American journal of medical genetics. Part A

Published: October 10, 2025

Mid‑trimester ultrasound findings in tricho‑hepato‑enteric syndrome: A case report.

Mid‑trimester ultrasound findings in tricho‑hepato‑enteric syndrome: A case report.

Journal: Biomedical reports

Published: February 12, 2025

Novel familial KDF1 mutation detected in members of a three-generation family with clinical manifestations of ectodermal dysplasia: A report of four cases.

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 Identification of a Missense Mutation of the L1CAM Gene Associated With Hydrocephalus Using Next-Generation Sequencing.

Prenatal Identification of a Missense Mutation of the L1CAM Gene Associated With Hydrocephalus Using Next-Generation Sequencing.

Journal: Cureus

Published: February 28, 2024

Cell‑free fetal DNA at 11‑13 weeks of gestation is not altered in complicated pregnancies.

Cell‑free fetal DNA at 11‑13 weeks of gestation is not altered in complicated pregnancies.

Journal: Biomedical reports

Published: June 19, 2023

Genital Abnormalities and Growth Retardation as Early Signs of Dilated Cardiomyopathy with Ataxia Syndrome.

Genital Abnormalities and Growth Retardation as Early Signs of Dilated Cardiomyopathy with Ataxia Syndrome.

Journal: Case reports in genetics

Published: June 12, 2023

An asymptomatic male individual carrying a 5.72 Mb de novo deletion in 8p23.2‑p23.3: A case report.

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.

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

Invasive Prenatal Diagnostic Testing for Aneuploidies in Singleton Pregnancies: A Comparative Review of Major Guidelines.

Invasive Prenatal Diagnostic Testing for Aneuploidies in Singleton Pregnancies: A Comparative Review of Major Guidelines.

Journal: Medicina (Kaunas, Lithuania)

Published: August 28, 2022

Showing 1-12 of 55

Last Updated: 09/26/2026