Clinical and genetic heterogeneity of primary ciliopathies (Review)

por Focşa, Ina Ofelia, Budişteanu, Magdalena, Bălgrădean, Mihaela
Publicado 2021

Treatment of Epilepsy Associated with Common Chromosomal Developmental Diseases

por Budisteanu, Magdalena, Jurca, Claudia, Papuc, Sorina Mihaela, Focsa, Ina, Riga, Dan, Riga, Sorin, Jurca, Alexandru, Arghir, Aurora
Publicado 2020

A case of Bardet-Biedl syndrome caused by a recurrent variant in BBS12: A case report

por Focșa, Ina Ofelia, Budișteanu, Magdalena, Burloiu, Carmen, Khan, Sheraz, Sadeghpour, Azita, Bohîlțea, Laurențiu C., Davis, Erica E., Bălgrădean, Mihaela
Publicado 2021