Cohen syndrome – a rare genetic cause of hypotonia in children

Por Budisteanu, Magdalena, Barca, Diana, Chirieac, Sorina Mihaela, Magureanu, Sanda
Publicado em 2010

Intellectual Disability and Epilepsy in Down Syndrome

Por BARCA, Diana, TARTA-ARSENE, Oana, DICA, Alice, ILIESCU, Catrinel, BUDISTEANU, Magdalena, MOTOESCU, Cristina, BUTOIANU, Niculina, CRAIU, Dana
Publicado no Maedica (Bucur) (2014)

Diagnostic Approach of Angelman Syndrome

Por DUCA, Denis George, CRAIU, Dana, BOER, Monica, CHIRIEAC, Sorina Mihaela, ARGHIR, Aurora, TUTULAN-CUNITA, Andreea, BARCA, Diana, ILIESCU, Catrinel, LUNGEANU, Agripina, MAGUREANU, Sanda, BUDISTEANU, Magdalena
Publicado em 2013

NBEA: developmental disease gene with early generalized epilepsy phenotypes

Por Mulhern, Maureen S., Stumpel, Constance, Stong, Nicholas, Brunner, Han G., Bier, Louise, Lippa, Natalie, Riviello, James, Rouhl, Rob P.W., Kempers, Marlies, Pfundt, Rolph, Stegmann, Alexander P.A., Kukolich, Mary K., Telegrafi, Aida, Lehman, Anna, Lopez-Rangel, Elena, Houcinat, Nada, Barth, Magalie, den Hollander, Nicolette, Hoffer, Mariette JV, Weckhuysen, Sarah, Roovers, Jolien, Djemie, Tania, Barca, Diana, Ceulemans, Berten, Craiu, Dana, Lemke, Johannes R., Korff, Christian, Mefford, Heather C., Meyers, Candace T., Siegler, Zsuzsanna, Hiatt, Susan M., Cooper, Gregory M., Bebin, E. Martina, Snijders-Blok, Lot, Veenstra-Knol, Hermine E., Baugh, Evan H., Brilstra, E.H., Volker-Touw, Catharina M.L., van Binsbergen, Ellen, Revah-Politi, Anya, Pereira, Elaine, McBrian, Danielle, Pacault, Mathilde, Isidor, Bertrand, Le Caignec, Cedric, Gilbert-Dussardier, Brigitte, Bilan, Frederic, Heinzen, Erin L., Goldstein, David B., Stevens, Servi J. C., Sands, Tristan T.
Publicado no Ann Neurol (2018)