5
5. Rodica Togănel, Claudia Bănescu, Carmen Duicu, Carmen Şuteu,
Iolanda Muntean,
Amalia Făgărăşan, et al. Angiotensin-converting enzyme gene
polymorphisms in
pulmonary arterial hypertension in children. Rev Romana Med Lab.
2010;18(4):31-36,
ISSN 1841-6624, cod CNCSIS 739 A, IF=0,113
6. Paşcanu I., Bănescu C., Benedek T., Duicu C., Csép K., Dema
A. Thyroid Dysfunction In
Children With Down’s Syndrome. Acta Endo (Buc), 2009, 1(V),
85-92, doi:
10.4183/aeb.2009.85 ISSN 1841-0987, cod CNCSIS 676 A,
IF=0.011
2.Articole publicate in extenso în reviste cotate ISI, fara
factor de impact,
autor principal
1. Claudia Bănescu, Ionela Paşcanu, Katalin Csép, István
Benedek, Erzsebét Benedek,
Carmen Duicu, et al. Cytogenetic analysis in acute myeloid
leukemia in Tîrgu Mureş.
Rev Romana Med Lab. 2008;13(4):21-29, ISSN 1841-6624, cod CNCSIS
739 A, revistă
cotată ISI, fara factor de impact
2. Paşcanu I., Borda A., Bănescu C. Thyroid nodule with
Hashimoto thyroiditis in
childhood – a challenging experience. Rom J Morphol Embryol.
2008; 49(4):541-5.
ISSN 1220-0522, cod CNCSIS 772 A, revistă cotată ISI, fara
factor de impact
3. Claudia Bănescu, István Benedek, Erzsébet Benedek, Ionela
Paşcanu, Katalin Csép,
Carmen Duicu, Demian Smaranda. Application of Cytogenetics for
Chronic Myeloid
Leukemia in Tîrgu Mureş. Rev Romana Med Lab. 2009;14(1):31-39,
ISSN 1841-6624,
cod CNCSIS 739 A, fara factor de impact
co-autor
1. Duicu C, Kiss E., Bănescu C., Bodescu V., Moreh Z., Horvath
E. Congenital nephrotic
syndrome of Finnish type - cases report. Rev Romana Med Lab.
2009;17(4):43-49.
ISSN 1841-6624, cod CNCSIS 739 A, revistă cotată ISI, fara
factor de impact
2. Paşcanu I., Todoran B. A. M., Csep K., Bănescu C., Togănel R.
A case of 49,XXXXY
syndrome in endocrine practice. Acta Endo (Buc), 2008, 4(IV),
455-463. ISSN 1841-
0987, cod CNCSIS 676 A, revistă cotată ISI, fara factor de
impact,
3. K.Csep, Gyongyi Dudutz, Marta Vitay, Ionela Paşcanu, Claudia
Bănescu, L. Koranyi, L.
Rosivall. The relationship between the PRO12ALA polymorphism of
the PPARγ2 gene
and the metabolic syndrome diagnosed in a population of central
Romania according
to the IDF criteria. Acta Endo (Buc), 2008, 3(IV): 263-271, ISSN
1841-0987, doi:
10.4183/aeb.2008.263,cod CNCSIS 676 A, indexata ISI, fara factor
de impact
Articole publicate in extenso în reviste BDI, autor principal /
coautor
BDI autor principal
1. Togănel R, Muntean I, Făgărăşan A, Gozar L, Pașc S, Șuteu C,
Bănescu C. Correlations
between three variants of MTHFR gene polymorphisms and
congenital heart defects
risk: a Romanian case-control study. Exp Clin Cardiol 2014,
20(10):6336-6344.
2. Ionela Pașcanu, Oana Maria Capraru, Otilia Mărginean, Claudia
Bănescu. Therapeutic
approach in Prader-Willi syndrome. Jurnalul Pediatrului,
XVI(63):32-37. CNCSIS code:
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