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J De Zaeytijd

Showing results (1-10 of 4) with videos related to

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Bulletin De La Societe Belge D'Ophtalmologie|February 3, 2005
Progressive cone dystrophy and sensorineural hearing lossJ A Witters, J De Zaeytijd, M Leys, et al.
Bulletin De La Societe Belge D'Ophtalmologie|June 14, 2014
Bifocal optic and facial nerve t-cell lymphomaA Van Hoey, A Shah, J De Zaeytijd, et al.
Multiple Sclerosis and Related Disorders|April 30, 2019
Biotinidase deficiency: A treatable cause of opticospinal syndrome in young adults<sup>✰</sup>V Van Iseghem, M Sprengers, J De Zaeytijd, et al.
Stem Cell Research|May 30, 2025
Generation of two iPSC lines (UGENTi003 and UGENTi004) from patients with intermediate rod-cone dystrophy carrying the c.[-123C>T;701G>A];[806_810del] variants in the RDH12 geneM Bouckaert, F Van Den Broeck, M Ghazvini, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Bulletin De La Societe Belge D'Ophtalmologie|February 3, 2005
Progressive cone dystrophy and sensorineural hearing lossJ A Witters, J De Zaeytijd, M Leys, et al.
Bulletin De La Societe Belge D'Ophtalmologie|June 14, 2014
Bifocal optic and facial nerve t-cell lymphomaA Van Hoey, A Shah, J De Zaeytijd, et al.
Multiple Sclerosis and Related Disorders|April 30, 2019
Biotinidase deficiency: A treatable cause of opticospinal syndrome in young adults<sup>✰</sup>V Van Iseghem, M Sprengers, J De Zaeytijd, et al.
Stem Cell Research|May 30, 2025
Generation of two iPSC lines (UGENTi003 and UGENTi004) from patients with intermediate rod-cone dystrophy carrying the c.[-123C>T;701G>A];[806_810del] variants in the RDH12 geneM Bouckaert, F Van Den Broeck, M Ghazvini, et al.
Pageof 1