Laboratory diagnosis and follow-up of Romanian Gaucher disease patients
Drugan, Cristina, Drugan, Tudor, Caillaud, Catherine, Grigorescu-Sido, Paula, Nistor, Tiberiu, Crăciun, Alexandra M.
Mucopolysaccharidosis type I - Clinical and genetic characteristics of Romanian patients
Alkhzouz, Camelia, Lazea, Cecilia, Miclea, Diana, Asavoaie, Carmen, Nascu, Ioana, Pop, Tudor, Grigorescu-Sido, Paula
Evaluation of c677t and a1298c polymorphism of the methylenetetrahydrofolate reductase gene as a maternal risk factor for trisomy 21 (a monocentric study)
Bucerzan, Simona, Popp, Radu Anghel, Vlad, Raluca Maria, Lazea, Cecilia, Nicolaescu, Radu, Grigorescu-Sido, Paula
Association between Cardiac Malformations and Karyotype in Turner Syndrome - a Single Centre Study
Lazea, Cecilia, Bucerzan, Simona, Al-Khzouz, Camelia, Cret, Victoria, Crisan, Mirela, Miclea, Diana, Grigorescu-Sido, Paula
GJB2 and GJB6 genes mutations in children with non-syndromic hearing loss
Lazăr, Călin, Popp, Radu, Al-Khzouz, Camelia, Mihuț, Gheorghe, Grigorescu-Sido, Paula