Ivana Dabaj
11PUBLICATIONS
45CO-AUTHORS
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Publications (11)
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|Mar 06, 2026
Laminopathies: natural history and risk prediction of heart failure.Philippe Charron, Julie Proukhnitzky, Rabah Ben Yaou
|Apr 03, 2025
Mannose Phosphate Isomerase Deficiency-Congenital Disorder of Glycosylation (MPI-CDG) Type 1b: Familial Case of Thrombophilia and Liver Disorder.Franklin Ducatez, Elisa Minacori, Sandrine Vuillaumier Barrot
|Dec 08, 2022
Variants in CLDN5 cause a syndrome characterized by seizures, microcephaly and brain calcifications.Ashish R Deshwar, Cheryl Cytrynbaum, Harsha Murthy
|Jul 27, 2022
Pontocerebellar Hypoplasia Type 1D: A Case Report and Comprehensive Literature Review.Ivana Dabaj, Adnan Hassani, Lydie Burglen
|Sep 28, 2021
An Atypical Case of Head Tremor and Extensive White Matter in an Adult Female Caused by 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency.Nassim Boutouchent, Julie Bourilhon, Bénédicte Sudrié-Arnaud
|Jul 09, 2021
International retrospective natural history study of LMNA-related congenital muscular dystrophy.Rabah Ben Yaou, Pomi Yun, Ivana Dabaj
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Frequent Collaborators
5 joint publications
Abdellah Tebani
5 joint publications
Soumeya Bekri
4 joint publications
Stéphane Marret
1 joint publications
Cyril Gitiaux
1 joint publications
Alessandro Amaddeo
1 joint publications
Sonia Khirani
1 joint publications
Brigitte Fauroux
1 joint publications
Myriam Vezain
1 joint publications
Maxime Fontanilles
1 joint publications
Hui Xiong
