Eleonora Dronca
Eleonora Dronca
Lecturer, Medical Genetics, Iuliu Hatieganu University of Medicine and Farmacy, Cluj
Verified email at umfcluj.ro
Cited by
Cited by
High levels of homocysteine and low serum paraoxonase 1 arylesterase activity in children with autism
SP Paşca, B Nemeş, L Vlase, CE Gagyi, E Dronca, AC Miu, M Dronca
Life sciences 78 (19), 2244-2248, 2006
One carbon metabolism disturbances and the C677T MTHFR gene polymorphism in children with autism spectrum disorders
SP Paşca, E Dronca, T Kaucsár, EC Crǎciun, E Endreffy, BK Ferencz, ...
Journal of cellular and molecular medicine 13 (10), 4229-4238, 2009
Serum homocysteine levels, oxidative stress and cardiovascular risk in non-alcoholic steatohepatitis
NV Leach, E Dronca, SC Vesa, DP Sampelean, EC Craciun, M Lupsor, ...
European Journal of internal medicine 25 (8), 762-767, 2014
Evaluation of whole blood zinc and copper levels in children with autism spectrum disorder
EC Crăciun, G Bjřrklund, AA Tinkov, MA Urbina, AV Skalny, F Rad, ...
Metabolic brain disease 31 (4), 887-890, 2016
Paraoxonase 1 activities and polymorphisms in autism spectrum disorders
SP Paşca, E Dronca, B Nemeş, T Kaucsár, E Endreffy, F Iftene, I Benga, ...
Journal of cellular and molecular medicine 14 (3), 600-607, 2010
Paraoxonase-1 activities in children and adolescents with type 1 diabetes mellitus
EC Craciun, DC Leucuta, RL Rusu, BA David, V Cret, E Dronca
Acta Biochimica Polonica 63 (3), 511-515, 2016
Low retinal dehydrogenase 1 (RALDH1) level in prepubertal boys with autism spectrum disorder: a possible link to dopamine dysfunction?
D Pavăl, F Rad, R Rusu, AŞ Niculae, HA Colosi, I Dobrescu, E Dronca
Clinical Psychopharmacology and Neuroscience 15 (3), 229, 2017
State of the art in human adipose stem cells and their role in therapy
AS Şovrea, AB Boşca, AM Constantin, E Dronca, A Ilea
Rom J Morphol Embryol 60 (1), 7-31, 2019
Antioxidant enzymes activity in subjects with Parkinson's disease under L-DOPA therapy
EC Crăciun, E Dronca, NV Leach
Human and Veterinary Medicine 8 (2), 124-127, 2016
Genotype-phenotype analysis of paraoxonase 1 in schizophrenic patients treated with atypical antipsychotics
D Pavăl, B Nemeş, RL Rusu, E Dronca
Clinical Psychopharmacology and Neuroscience 16 (1), 32, 2018
Chondroprotective effects of pulsed shortwave therapy in rabbits with experimental osteoarthritis
RA Ungur, A Florea, AF Tăbăran, IC Scurtu, I Onac, IM Borda, L Irsay, ...
Rom J Morphol Embryol 58 (2), 465-72, 2017
Diagnostic correlation between RET proto-oncogene mutation, imaging techniques, biochemical markers and morphological examination in MEN2A syndrome: case report and literature …
AS Sovrea, E Dronca, M Galatar, S Radian, C Vornicescu, C Georgescu
Rom J Morphol Embryol 55 (2), 389-400, 2014
Low Serum Paraoxonase-1 Lactonase and Arylesterase Activities in Obese Children and Adolescents
R Sandor, D Leucuta, E Dronca, A Niculae, V Cret, C Silaghi, S Suciu
Revista Romana de Medicina de Laborator 23 (4), 385-396, 2015
Paraoxonase 1 genotype–phenotype correlation in patients with metabolic syndrome
L Ciumărnean, E Dronca, ŞC Vesa, D Sâmpelean, AD Buzoianu, ...
Rom J Morphol Embryol 56 (2), 387-392, 2015
Interplay between metabolic and thyroid parameters in obese pubertal children. Does visceral adipose tissue make the first move?
N Răcătăianu, NV Leach, SD Bolboacă, ML Soran, O Opriş, E Dronca, ...
Acta Clinica Belgica 76 (1), 40-48, 2021
Vitamin D deficiency, insulin resistance and thyroid dysfunction in obese patients: is inflammation the common link?
N Răcătăianu, NV Leach, SD Bolboacă, A Cozma, E Dronca, A Valea, ...
Scandinavian journal of clinical and laboratory investigation 78 (7-8), 560-565, 2018
Understanding BRCA1 and BRCA2 mutated breast cancer cases in Romania: First report on founder mutations in Romanians
A Eniu, L Pop, A Stoian, E Dronca, R Matei, M Ligtenberg, H Ouchene, ...
Annals of Oncology 28, v60-v61, 2017
Distribution of Paraoxonase 1 polymorphisms and activities in obese patients
L Ciumărnean, ŞC Vesa, E Dronca, DP Sâmpelean, VC Vlad, ...
Revista Romana de Medicina de Laborator 21 (4), 381-389, 2013
BRCA 1/2 mutations by next-generation sequencing testing in 200 Romanian high-risk patients with breast cancer.
AE Eniu, NZ Antone, A Stoian, E Dronca, RD Matei, M Ligtenberg, ...
Journal of Clinical Oncology 35 (15_suppl), e13116-e13116, 2017
Diagnostic difficulties in chronic kidney disease–Is it or is it not Fabry disease?
L Ciumărnean, I Para, T Alexescu, E Dronca, B Szolga, MV Milaciu
Kidney 8, 9, 2017
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