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Gorduza EV
Gorduza EV
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Title
Cited by
Cited by
Year
Bardet–Biedl syndrome—Multiple kaleidoscope images: insight into mechanisms of genotype–phenotype correlations
L Florea, L Caba, EV Gorduza
Genes 12 (9), 1353, 2021
422021
Increased nuchal translucency in fetuses with a normal karyotype—diagnosis and management An observational study
PI Socolov D., Socolov R., Gorduza E.V., Butureanu T., Stanculescu R ...
Medicine 96 (29), e7521, 2017
312017
Circular RNA—Is the Circle Perfect?
L Caba, L Florea, C Gug, DC Dimitriu, EV Gorduza
Biomolecules 11 (12), 1755, 2021
302021
Holt-Oram syndrome with multiple cardiac abnormalities
MR Spiridon, AO Petris, EV Gorduza, AS Petras, R Popescu, L Caba
Cardiology research 9 (5), 324, 2018
282018
Genetic modifying factors of cystic fibrosis phenotype: a challenge for modern medicine
LI Butnariu, E Țarcă, E Cojocaru, C Rusu, ȘM Moisă, ...
Journal of Clinical Medicine 10 (24), 5821, 2021
272021
Ring autosomes: some unexpected findings
L Caba, C Rusu, V Plăiaşu, G Gug, M Grămescu, C Bujoran, D Ochiană, ...
Balkan Journal of Medical Genetics 15 (2), 35-46, 2012
252012
Clinical and cytogenetic correlation in primary and secondary amenorrhea: retrospective study on 531 patients
L Butnariu, M Covic, I Ivanov, C Bujoran, M Gramescu, EV Gorduza
Revista Română de Medicină de Laborator 19 (2/4), 2011
232011
Etiologic puzzle of coronary artery disease: how important is genetic component?
LI Butnariu, L Florea, MC Badescu, E Țarcă, II Costache, EV Gorduza
Life 12 (6), 865, 2022
212022
Rare splicing mutation in COL1A1 gene identified by whole exomes sequencing in a patient with osteogenesis imperfecta type I followed by prenatal diagnosis: A case report and …
C Gug, L Caba, I Mozos, D Stoian, D Atasie, M Gug, EV Gorduza
Gene 741, 144565, 2020
182020
Wolf-Hirschhorn syndrome: clinical and genetic study of 7 new cases, and mini review
EC Gavril, AC Luca, AS Curpan, R Popescu, I Resmerita, MC Panzaru, ...
Children 8 (9), 751, 2021
172021
Genetics of Hearing Impairment in North-Eastern Romania—A Cost-Effective Improved Diagnosis and Literature Review
I Resmerita, RS Cozma, R Popescu, LM Radulescu, MC Panzaru, ...
Genes 11 (12), 1506, 2020
152020
Nutrigenomics in postgenomic era.
EV Gorduza, LL Indrei, VM Gorduza
Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi …, 2008
152008
Gorham-stout disease with multiple bone involvement—challenging diagnosis of a rare disease and literature review
A Momanu, L Caba, NC Gorduza, OE Arhire, AD Popa, V Ianole, ...
Medicina 57 (7), 681, 2021
142021
Genetic counselling in reproductive disorders
GC Cozaru, LI Butnariu, EV Gorduza
Procedia-Social and Behavioral Sciences 33, 213-217, 2012
142012
Structure-reactivity relationships of antioxidant flavonoides
V Gorduza, C Tarabasanu, A Gorduza, C Cernatescu, M Rusu
Ovidius University Annals of Chemistry 11 (1), 56-59, 2000
142000
Genetic heterogeneity in Bartter syndrome: clinical and practical importance
L Florea, L Caba, EV Gorduza
Frontiers in Pediatrics 10, 908655, 2022
132022
Genetic counseling and management: the first study to report NIPT findings in a Romanian population
C Gug, I Mozos, A Ratiu, A Tudor, EV Gorduza, L Caba, M Gug, ...
Medicina 58 (1), 79, 2022
132022
Comparison between paramagnetic and CD71 magnetic activated cell sorting of fetal nucleated red blood cells from the maternal blood
D Nemescu, D Constantinescu, V Gorduza, A Carauleanu, L Caba, ...
Journal of Clinical Laboratory Analysis 34 (9), e23420, 2020
132020
CHARGE syndrome associated with de novo (I1460Rfs* 15) frameshift mutation of CHD7 gene in a patient with arteria lusoria and horseshoe kidney
C Gug, EV Gorduza, A Lăcătuşu, MA Vaida, F Bîrsăşteanu, M Puiu, ...
Experimental and therapeutic medicine 20 (1), 479-485, 2020
132020
Polyploidy in First and Second Trimester Pregnancies in Romania-a Retrospective Study.
C Gug, F Burada, M Ioana, AL Riza, M Moldovan, I Mozos, A Ratiu, ...
Clinical laboratory 86 (4), 2020
132020
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