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

Phenotype Heterogeneity in 3q29 Microduplication Syndrome

por STREATA, IOANA, RIZA, ANCA-LELIA, SOSOI, SIMONA, BURADA, FLORIN, IOANA, MIHAI
Publicado 2020

The Role of Vitamin D in Obese Children with Non-Alcoholic Fatty Liver Disease and Associated Metabolic Syndrome

por Stepan, Mioara Desdemona, Vintilescu, Ștefănița Bianca, Streață, Ioana, Podeanu, Mihaela Andreea, Florescu, Dan Nicolae
Publicado 2023

Determination of iNOS-2087A>G Polymorphism in Acute Pancreatitis Patients

por PĂDUREANU, V., STREAȚĂ, IOANA, IOANA, M., ȘURLIN, V., GEORGESCU, E.F., MĂRGINEAN, CRISTINA, SĂFTOIU, A.
Publicado 2014

Interleukin-8 mRNA Expression in Locally Advanced Colorectal Cancer Patients

por BĂRBĂLAN, A., STREAȚA, IOANA, IVAN, ELENA TATIANA, CHERCIU, IRINA, ȘURLIN, V., IOANA, M., SĂFTOIU, A.
Publicado 2017

Heart function assessment during aging in apolipoprotein E knock-out mice

por Liehn, Elisa A., Lupan, Ana-Mihaela, Diaconu, Rodica, Ioana, Mihai, Streata, Ioana, Manole, Catalin, Burlacu, Alexandrina
Publicado 2021

Autistic Behavior as Novel Clinical Finding in OFD1 Syndrome

por Papuc, Sorina Mihaela, Erbescu, Alina, Glangher, Adelina, Streata, Ioana, Riza, Anca-Lelia, Budisteanu, Magdalena, Arghir, Aurora
Publicado 2023

Expanding the Clinical Phenotype of 19q Interstitial Deletions: A New Case with 19q13.32-q13.33 Deletion and Short Review of the Literature

por Shelby, Elena-Silvia, Morris, Michael, Pădure, Liliana, Mirea, Andrada, Cocoș, Relu, Cărămizaru, Alexandru, Șerban-Sosoi, Simona, Pîrvu, Andrei, Streață, Ioana
Publicado 2022

Association between genetic variants and depression in a Romanian cohort

por Costache, Andrei, Riza, Anca-Lelia, Popescu, Mihaela, Streaţă, Ioana, Dincă, Mihaela-Eugenia, Glăvan, Daniela Gabriela, Vladu, Ionela Mihaela, Udriştoiu, Ion, Ioana, Mihai
Publicado 2021

Serum Amino Acid Profiling in Children with Autistic Spectrum Disorder: Insights from a Single-Center Study in Southern Romania

por Anastasescu, Cătălina Mihaela, Gheorman, Veronica, Popescu, Florica, Stoicănescu, Eugen-Cristi, Gheorman, Victor, Riza, Anca-Lelia, Badea, Oana, Streață, Ioana, Militaru, Felicia, Udriștoiu, Ion
Publicado 2023

The CARD9 Polymorphisms rs4077515, rs10870077 and rs10781499 Are Uncoupled from Susceptibility to and Severity of Pulmonary Tuberculosis

por Streata, Ioana, Weiner, January, Iannaconne, Marco, McEwen, Gayle, Ciontea, Marius Sorin, Olaru, Marian, Capparelli, Rosanna, Ioana, Mihai, Kaufmann, Stefan H. E., Dorhoi, Anca
Publicado 2016

Correction: The CARD9 Polymorphisms rs4077515, rs10870077 and rs10781499 Are Uncoupled from Susceptibility to and Severity of Pulmonary Tuberculosis

por Streata, Ioana, Weiner, January, Iannaccone, Marco, McEwen, Gayle, Ciontea, Marius Sorin, Olaru, Marian, Capparelli, Rosanna, Ioana, Mihai, Kaufmann, Stefan H. E., Dorhoi, Anca
Publicado 2016

Prenatal diagnosis of a pure 15q distal trisomy derived from a maternal pericentric inversion: A case report

por Burada, Florin, Streata, Ioana, Ungureanu, Anda, Ruican, Dan, Nagy, Rodica, Serban-Sosoi, Simona, Stambouli, Danai, Dimos, Luiza, Popescu-Hobeanu, Gabriela, Mihai, Ioana, Iliescu, Dominic
Publicado 2021

Assessing Putative Markers of Colorectal Cancer Stem Cells: From Colonoscopy to Gene Expression Profiling

por Harbiyeli, Irina Florina Cherciu, Burtea, Daniela Elena, Ivan, Elena Tatiana, Streață, Ioana, Nicoli, Elena Raluca, Uscatu, Daniel, Șerbănescu, Mircea-Sebastian, Ioana, Mihai, Vilmann, Peter, Săftoiu, Adrian
Publicado 2022

PAH Pathogenic Variants and Clinical Correlations in a Group of Hyperphenylalaninemia Patients from North-Western Romania

por Iuhas, Alin, Jurca, Claudia, Kozma, Kinga, Riza, Anca-Lelia, Streață, Ioana, Petcheși, Codruța, Dan, Andra, Sava, Cristian, Balmoș, Andreea, Marinău, Cristian, Niulaș, Larisa, Ioana, Mihai, Bembea, Marius
Publicado 2023

Human Monocytic Suppressive Cells Promote Replication of Mycobacterium tuberculosis and Alter Stability of in vitro Generated Granulomas

por Agrawal, Neha, Streata, Ioana, Pei, Gang, Weiner, January, Kotze, Leigh, Bandermann, Silke, Lozza, Laura, Walzl, Gerhard, du Plessis, Nelita, Ioana, Mihai, Kaufmann, Stefan H. E., Dorhoi, Anca
Publicado 2018

Genetic Testing for Familial Hypercholesterolemia in a Pediatric Group: A Romanian Showcase

por Constantin, Andreea Teodora, Streata, Ioana, Covăcescu, Mirela Silvia, Riza, Anca Lelia, Roșca, Ioana, Delia, Corina, Tudor, Lucia Maria, Dorobanțu, Ștefania, Dragoș, Adina, Ristea, Diana, Ioana, Mihai, Gherghina, Ioan
Publicado 2023

The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 Patients

por Budisteanu, Magdalena, Papuc, Sorina Mihaela, Streata, Ioana, Cucu, Mihai, Pirvu, Andrei, Serban-Sosoi, Simona, Erbescu, Alina, Andrei, Emanuela, Iliescu, Catrinel, Ioana, Doina, Severin, Emilia, Ioana, Mihai, Arghir, Aurora
Publicado 2021

Phenotypic and Genotypic Spectrum of Early-Onset Developmental and Epileptic Encephalopathies—Data from a Romanian Cohort

por Riza, Anca-Lelia, Streață, Ioana, Roza, Eugenia, Budișteanu, Magdalena, Iliescu, Catrinel, Burloiu, Carmen, Dobrescu, Mihaela-Amelia, Dorobanțu, Stefania, Dragoș, Adina, Grigorescu, Andra, Tătaru, Tiberiu, Ioana, Mihai, Teleanu, Raluca
Publicado 2022

Pathogenic Copy Number Variations Involved in the Genetic Etiology of Syndromic and Non-Syndromic Intellectual Disability—Data from a Romanian Cohort

por Streață, Ioana, Caramizaru, Alexandru, Riza, Anca-Lelia, Șerban-Sosoi, Simona, Pîrvu, Andrei, Cara, Monica-Laura, Cucu, Mihai-Gabriel, Dobrescu, Amelia Mihaela, Shelby, Elena-Silvia, Albeanu, Adriana, Burada, Florin, Ioana, Mihai
Publicado 2022