Role of salivary miRNAs in the diagnosis of gastrointestinal disorders: a mini-review of available evidence

por Săsăran, Maria Oana, Bănescu, Claudia
Publicado 2023

The Genetic Landscape of Myelodysplastic Neoplasm Progression to Acute Myeloid Leukemia

por Bănescu, Claudia, Tripon, Florin, Muntean, Carmen
Publicado 2023

Molecular diagnosis methods in familial hypercholesterolemia

por Moldovan, Valeriu, Banescu, Claudia, Dobreanu, Minodora
Publicado 2020

From Descriptive to Functional Genomics of Leukemias Focusing on Genome Engineering Techniques

por Balla, Beata, Tripon, Florin, Banescu, Claudia
Publicado 2021

Diabetic kidney disease in pediatric patients: A current review

por Muntean, Carmen, Starcea, Iuliana Magdalena, Banescu, Claudia
Publicado 2022

PAX2 Gene Mutation in Pediatric Renal Disorders—A Narrative Review

por Muntean, Carmen, Chirtes, Camelia, Baczoni, Balazs, Banescu, Claudia
Publicado 2023

Copy Number Variations and Gene Mutations Identified by Multiplex Ligation-Dependent Probe Amplification in Romanian Chronic Lymphocytic Leukemia Patients

por Balla, Beata, Tripon, Florin, Candea, Marcela, Banescu, Claudia
Publicado 2023

Response to: Comment on “Factors Associated with Recurrent Ulcers in Patients with Gastric Surgery after More Than 15 Years: A Cross-Sectional Single-Center Study”

por Negovan, Anca, Pantea, Monica, Banescu, Claudia, Mocan, Simona
Publicado 2019

Helicobacter pylori and cytokine gene variants as predictors of premalignant gastric lesions

por Negovan, Anca, Iancu, Mihaela, Fülöp, Emőke, Bănescu, Claudia
Publicado 2019

Exon 21 deletion in the OPHN1 gene in a family with syndromic X-linked intellectual disability: Case report

por Bogliş, Alina, Cosma, Adriana S., Tripon, Florin, Bãnescu, Claudia
Publicado 2020

Pathogenic Biallelic Mutations in ECHS1 in a Case with Short-Chain Enoyl-CoA Hydratase (SCEH) Deficiency-Case Report and Literature Review

por Muntean, Carmen, Tripon, Florin, Bogliș, Alina, Bănescu, Claudia
Publicado 2022

Clinical Characteristics, Renal Involvement, and Therapeutic Options of Pediatric Patients With Fabry Disease

por Muntean, Carmen, Starcea, Iuliana Magdalena, Stoica, Cristina, Banescu, Claudia
Publicado 2022

Corrigendum: Clinical characteristics, renal involvement, and therapeutic options of pediatric patients with Fabry disease

por Muntean, Carmen, Starcea, Iuliana Magdalena, Stoica, Cristina, Banescu, Claudia
Publicado 2022

Helicobacter pylori-Positive Gastric Biopsies—Association with Clinical Predictors

por Negovan, Anca, Szőke, Andreea-Raluca, Mocan, Simona, Bănescu, Claudia
Publicado 2022

Effects of PPARG and PPARGC1A gene polymorphisms on obesity markers

por Muntean, Carmen, Sasaran, Maria Oana, Crisan, Adriana, Banescu, Claudia
Publicado 2022

Compound heterozygous FAM20C gene variants in a patient with severe Raine syndrome: a case report

por Chirteș, Camelia, Bogliș, Alina, Toth, Andrea, Rac, Corina, Bănescu, Claudia
Publicado 2023

The Role of Galectin-3 in Predicting Congenital Heart Disease Outcome: A Review of the Literature

por Făgărășan, Amalia, Săsăran, Maria, Gozar, Liliana, Crauciuc, Andrei, Bănescu , Claudia
Publicado 2023

The Interaction between GSTT1, GSTM1, and GSTP1 Ile105Val Gene Polymorphisms and Environmental Risk Factors in Premalignant Gastric Lesions Risk

por Negovan, Anca, Iancu, Mihaela, Moldovan, Valeriu, Mocan, Simona, Banescu, Claudia
Publicado 2017

Study of rs12532, rs8670 Polymorphism of Msh Homeobox 1 (MSX1), rs61754301, rs4904155 Polymorphism of Paired Box Gene 9 (PAX9), and rs2240308 Polymorphism of Axis Inhibitor Protein...

por Mártha, Krisztina, Kerekes Máthé, Bernadette, Moldovan, Valeriu George, Bănescu, Claudia
Publicado 2019

Pitt-Hopkins Syndrome: Clinical and Molecular Findings of a 5-Year-Old Patient

por Tripon, Florin, Bogliș, Alina, Micheu, Cristian, Streață, Ioana, Bănescu, Claudia
Publicado 2020