Dr. Mihaela Danila

Cursuri postuniversitare:

2020 : Proiectul de Formare profesionala a personalului din sistemul medical din Romania in genetica medicala PROGEN_107623;
2019: Stagiu de pregatire practica an Genetica Medicala clinica adulti si copii, diagnostic prenatal si genetica moleculara in cadrul proiectului PROGEN, Torino, Italia.

2021: ”Phenotype in Associated SMA mutations – experience of 5 years”, European Human Genetics Journal
2021: ”High risk pregnancy for achondroplasia and the importance of IgG avidity test for dating the infection with toxoplasma gondii ” Case report to the Medical-Surgical Journal
2020: ”Clinical and genetic characteristics of syndromes associated with craniosynostosis” , European Human Genetics Journal
2019: ”Nonsense mutation in Duchenne muscular dystrophy” - case report, Romanian Journal of Rare Diseases
2019: Asociatia de Medicina de Laborator din Romania, ”Spectrul mutatiilor fibrozei chistice in populatia din partea de Nord-Est a Romaniei”;
2019: E-Book, Proceedings of 5-th Medical Genetics Congress with International Participation, 26-28 September, ”A Deeper Understanding of Cystic Fibrosis – A Case Report”, Danila Mihaela, Panzaru Monica, Popescu Roxana, Tonu Maria, Resmerita Irina, Mihaila Doina, Rusu Cristina;
2019: E-Book, Proceedings of 5-th Medical Genetics Congress with International Participation, 26-28 September, ”Spondyloepiphyseal Dysplasia Congenita – A Case Report”, TONU Maria, Popescu Roxana, Danila Mihaela, Rusu Cristina”
2018: Romanian Journal of Rare Diseases, ”Mayer-Rokitansky-Kuster-Hauser Syndrom Type 2 – A case report”;