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Biomedicines|February 27, 2026
US-ATHC: Unsupervised Multi-Class Glioma Segmentation via Adaptive Thresholding and ClusteringJihan Alameddine, Céline Thomarat, Xavier Le-Guillou, et al.
Journal of Clinical Medicine|December 23, 2023
Diagnostic and Therapeutic Issues in Glioma Using Imaging Data: The Challenge of Numerical TwinningRémy Guillevin, Mathieu Naudin, Pierre Fayolle, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 8, 2024
Care pathways in childhood neurodevelopmental disorders: Toward greater awareness of KBG syndrome among pediatriciansMarie Adamo-Croux, Adriane Auger-Gilli, Gwenaël Le Guyader, et al.
Clinical Genetics|January 23, 2025
Exploring the Familial Phenotypic Variability Associated With TTN Truncating Variants in Cardiomyopathies: Variant Spectrum, Genotype-Phenotype Correlation and Consequences in Genetic CounselingMarie Massier, Pascal de Groote, Erwan Donal, et al.
Archives of Cardiovascular Diseases|December 3, 2019
Number of electrocardiogram leads in the diagnosis of spontaneous Brugada syndromeMarine Arnaud, Pauline Berthome, Romain Tixier, et al.
Thrombosis Research|July 12, 2023
Antiplatelet and anticoagulant therapies in hereditary hemorrhagic telangiectasia: A large French cohort study (RETROPLACOTEL)Vincent Grobost, Sami Hammi, Bruno Pereira, et al.
Angiogenesis|December 24, 2024
Effect of oral nintedanib vs placebo on epistaxis in hereditary hemorrhagic telangiectasia: the EPICURE multicenter randomized double-blind trialRuben Hermann, Vincent Grobost, Xavier Le-Guillou, et al.
European Journal of Human Genetics : EJHG|September 22, 2025
Further phenotypical delineation of DLG3-related neurodevelopmental disordersMarlène Malbos, Thierry Gautier, Amelle Shillington, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 31, 2023
YWHAE loss of function causes a rare neurodevelopmental disease with brain abnormalities in human and mouseAnne-Sophie Denommé-Pichon, Stephan C Collins, Ange-Line Bruel, et al.
Human Molecular Genetics|May 17, 2023
ANK2 loss-of-function variants are associated with epilepsy, and lead to impaired axon initial segment plasticity and hyperactive network activity in hiPSC-derived neuronal networksMaria W A Teunissen, Elly Lewerissa, Eline J H van Hugte, et al.
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