Ludmila Kousoulidou

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 7

Top Venues

Genes

American journal of medical genetics. Part A

Clinical case reports

Journal of human genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Andrea Hadjipanteli, Athina Theodosiou, Ioannis Papaevripidou, Paola Evangelidou, Angelos Alexandrou, Nicole Salameh, Ioannis Kallikas, Kyriakos Kakoullis, Sofia Frakala, Christina Oxinou, Andreas Marnerides, Ludmila Kousoulidou, Violetta C Anastasiadou, Carolina Sismani
Sodium Channel Gene Variants in Fetuses with Abnormal Sonographic Findings: Expanding the Prenatal Phenotypic Spectrum of Sodium Channelopathies. Genes 15 (1) (2024)
Andrea Hadjipanteli, Athina Theodosiou, Ioannis Papaevripidou, Paola Evangelidou, Angelos Alexandrou, Nicole Salameh, Ioannis Kallikas, Kyriakos Kakoullis, Sofia Frakala, Christina Oxinou, Andreas Marnerides, Ludmila Kousoulidou, Violetta C Anastasiadou, Carolina Sismani
Sodium Channel Gene Variants in Fetuses with Abnormal Sonographic Findings: Expanding the Prenatal Phenotypic Spectrum of Sodium Channelopathies. Genes 15 (1) (2024)
Andrea Hadjipanteli, Athina Theodosiou, Ioannis Papaevripidou, Paola Evangelidou, Angelos Alexandrou, Nicole Salameh, Ioannis Kallikas, Kyriakos Kakoullis, Sofia Frakala, Christina Oxinou, Andreas Marnerides, Ludmila Kousoulidou, Violetta C Anastasiadou, Carolina Sismani
Sodium Channel Gene Variants in Fetuses with Abnormal Sonographic Findings: Expanding the Prenatal Phenotypic Spectrum of Sodium Channelopathies. Genes 15 (1) (2024)
Andrea Hadjipanteli, Athina Theodosiou, Ioannis Papaevripidou, Paola Evangelidou, Angelos Alexandrou, Nicole Salameh, Ioannis Kallikas, Kyriakos Kakoullis, Sofia Frakala, Christina Oxinou, Andreas Marnerides, Ludmila Kousoulidou, Violetta C Anastasiadou, Carolina Sismani
Sodium Channel Gene Variants in Fetuses with Abnormal Sonographic Findings: Expanding the Prenatal Phenotypic Spectrum of Sodium Channelopathies. Genes 15 (1) (2024)
Carolina Sismani, Stamatia-Maria Rapti, Pavlina Iliopoulou, Anastasia Spring, Rozalia Neroutsou, Magdalini Lagou, Marianna Robola, Efstathios Tsitsopoulos, Ludmila Kousoulidou, Angelos Alexandrou, Ioannis Papaevripidou, Athina Theodosiou, Maria Syrrou, Sigrid Fuchs, Maja Hempel, Dagmar Huhle, Thomas Liehr, Monika Ziegler, Max Duesberg, Voula Velissariou
Novel pericentric inversion inv(9)(p23q22.3) in unrelated individuals with fertility problems in the Southeast European population. Journal of human genetics 65 (9) (2020)
Angelos Alexandrou, Ioannis Papaevripidou, Ioanna Maria Alexandrou, Athina Theodosiou, Paola Evangelidou, Ludmila Kousoulidou, George Tanteles, Violetta Christophidou-Anastasiadou, Carolina Sismani
De novo mosaic MECP2 mutation in a female with Rett syndrome. Clinical case reports 7 (2) (2019)
Ludmila Kousoulidou, Angelos Alexandrou, Ioannis Papaevripidou, Paola Evangelidou, George Tanteles, Violetta C Anastasiadou, Carolina Sismani
Two unrelated individuals carrying rare mosaic deletions in TCF4 gene. American journal of medical genetics. Part A 179 (1) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Ludmila Kousoulidou