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Showing 1-12 of 12 for the term ""Tripon, Florin""

A rare case of acute myeloid leukemia with ARHGEF12 (LARG, 11q23.3) and MAPRE1 (EB1, 20q11.21) fusion gene in an elderly patient
Article

A rare case of acute myeloid leukemia with ARHGEF12 (LARG, 11q23.3) and MAPRE1 (EB1, 20q11.21) fusion gene in an elderly patient

Macarie, Ioan, Tripon, Florin, Dorcioman, Bogdana, Macarie, Melania
Genetic variability of ANG2-35G>C gene as a predictor factor in sepsis
Article

Genetic variability of ANG2-35G>C gene as a predictor factor in sepsis

Szederjesi, Janos, Lazar, Alexandra, Petrisor, Marius, Hutanu, Adina, Tripon, Florin, Georgescu, Anca Meda, Azamfirei, Leonard
SH2B3 (LNK) rs3184504 polymorphism is correlated with JAK2 V617F-positive myeloproliferative neoplasms
Article

SH2B3 (LNK) rs3184504 polymorphism is correlated with JAK2 V617F-positive myeloproliferative neoplasms

Trifa, Adrian P., Lighezan, Diana L., Jucan, Cristina, Tripon, Florin, Arbore, Dana R., Bojan, Anca, Gligor-Popa, Ștefana, Pop, Raluca M., Dima, Delia, Bănescu, Claudia
Genetic Investigation and Clinical Aspects in a Romanian Treacher Collins Syndrome Family – A Case Report
Article

Genetic Investigation and Clinical Aspects in a Romanian Treacher Collins Syndrome Family – A Case Report

Anciuc, Mădălina, Tripon, Florin, Duicu, Carmen, Gliga, Carmen, Bănescu, Claudia
Multiplex ligation dependent probe amplification - A useful, fast and cost-effective method for identification of small supernumerary marker chromosome in children with developmental delay and congenital heart defect
Article

Multiplex ligation dependent probe amplification - A useful, fast and cost-effective method for identification of small supernumerary marker chromosome in children with developmental delay and congenital heart defect

Crauciuc, George Andrei, Tripon, Florin, Bogliş, Alina, Făgărăşan, Amalia, Bănescu, Claudia
Simultaneous FLT3, NPM1 and DNMT3A mutations in adult patients with acute myeloid leukemia – case study
Article

Simultaneous FLT3, NPM1 and DNMT3A mutations in adult patients with acute myeloid leukemia – case study

Tripon, Florin, Crauciuc, George Andrei, Moldovan, Valeriu George, Bogliș, Alina, Benedek, István, Lázár, Erzsébet, Bănescu, Claudia
The Influence of GPX1 Pro198Leu, CAT C262T and MnSOD Ala16Val Gene Polymorphisms on Susceptibility for Non-Hodgkin Lymphoma and Overall Survival Rate at Five Years from Diagnosis
Article

The Influence of GPX1 Pro198Leu, CAT C262T and MnSOD Ala16Val Gene Polymorphisms on Susceptibility for Non-Hodgkin Lymphoma and Overall Survival Rate at Five Years from Diagnosis

Cosma, Adriana-Stela, Radu, Cristina, Moldovan, Alexandra, Bogliș, Alina, Crauciuc, George Andrei, Horváth, Emőke, Cândea, Marcela, Tripon, Florin
The angiotensinogen gene polymorphism, lifestyle factors, associated diseases and gastric areas of inflammatory and preneoplastic lesions in a Romanian sample of patients
Article

The angiotensinogen gene polymorphism, lifestyle factors, associated diseases and gastric areas of inflammatory and preneoplastic lesions in a Romanian sample of patients

Anciuc, Mădălina, Tripon, Florin, Crauciuc, George-Andrei, Mocan, Simona, Negovan, Anca
Review. Development, Applications, Benefits, Challenges and Limitations of the New Genome Engineering Technique. An Update Study
Article

Review. Development, Applications, Benefits, Challenges and Limitations of the New Genome Engineering Technique. An Update Study

Crauciuc, Andrei, Tripon, Florin, Gheorghiu, Andreea, Nemes, Georgiana, Boglis, Alina, Banescu, Claudia
An Update on the Genetic Aspects in Congenital Ventricular Septal Defect
Article

An Update on the Genetic Aspects in Congenital Ventricular Septal Defect

Crauciuc, George Andrei, Tripon, Florin, Anciuc, Mădălina, Balla, Beata Magdolna, Bănescu, Claudia
Deep Venous Thrombosis Associated With Inferior Vena Cava Abnormalities And Hypoplastic Kidney In Siblings
Article

Deep Venous Thrombosis Associated With Inferior Vena Cava Abnormalities And Hypoplastic Kidney In Siblings

Duicu, Carmen, Bucur, Gabriela, Simu, Iunius, Tripon, Florin, Marginean, Oana
The utility of molecular genetic techniques in craniosynostosis cases associated with intellectual disability
Article

The utility of molecular genetic techniques in craniosynostosis cases associated with intellectual disability

Bogliş, Alina, Tripon, Florin, Bănescu, Claudia