Search Results - "Burada, Florin"

The Association between Nod2 R702w Polymorphism and Susceptibility to Colorectal Cancer in Romanian Patients.

Authors: BURADA, FLORIN MIREA, CECIL SORIN CUCU, MIHAI GABRIEL et al.

Source: Current Health Sciences Journal. Apr-Jun2018, Vol. 44 Issue 2, p135-139. 5p.

Association of microRNA Polymorphisms with the Risk of Gastric Cancer in a Romanian Population.

Authors: Rogoveanu, Ion Burada, Florin Cucu, Mihai Gabriel et al.

Source: Journal of Gastrointestinal & Liver Diseases. Sep2017, Vol. 26 Issue 3, p231-238. 8p.

IRGM gene polymorphisms and risk of gastric cancer.

Authors: BURADA, Florin PLANTINGA, Theo S IOANA, Mihai et al.

Source: Journal of Digestive Diseases. Jul2012, Vol. 13 Issue 7, p360-365. 6p.

Challenges in Diagnosis and Management of Coffin–Lowry Syndrome—Single-Center Experience.

Authors: Chirilas, Ana Maria Cărămizaru, Alexandru Riza, Anca-Lelia et al.

Source: Diagnostics (2075-4418). Apr2026, Vol. 16 Issue 7, p990. 15p.

Phenotypic Spectrum in Three Romanian Patients with 8q23–q24 Deletions.

Authors: Caramizaru, Alexandru Streata, Ioana Pirvu, Andrei et al.

Source: International Journal of Molecular Sciences. Feb2026, Vol. 27 Issue 3, p1249. 10p.

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

Authors: Burada, Florin Streata, Ioana Ungureanu, Anda et al.

Source: Experimental & Therapeutic Medicine. Apr2021, Vol. 21 Issue 4, pN.PAG-N.PAG. 1p.

From Diagnosis to Decision—Fetal Limb Abnormalities.

Authors: Stancioi-Cismaru, Andreea Florentina Capitanescu, Razvan Grigoras Naidin, Mihaela-Simona et al.

Source: Journal of Clinical Medicine. Jan2026, Vol. 15 Issue 2, p486. 16p.

Whole Exome Sequencing for Romanian Patients With Neurodevelopmental Disorders Through an International Collaboration.

Authors: Caramizaru, Alexandru Durac, Cristina Dumitrescu, Andreea et al.

Source: Clinical Genetics. Jul2026, Vol. 110 Issue 1, p46-63. 18p.

GAS5 rs145204276 Ins/Del Polymorphism Is Associated with CRC Susceptibility in a Romanian Population †.

Authors: Mirea, Cecil Sorin Schenker, Michael Petre-Mandache, Bianca et al.

Source: International Journal of Molecular Sciences. Apr2025, Vol. 26 Issue 7, p3078. 12p.

Chromosome Abnormality Detection Rates of QF-PCR in Early Pregnancy Loss.

Authors: POPESCU-HOBEANU, GABRIELA CUCU, MIHAI-GABRIEL RIZA, ANCA-LELIA et al.

Source: Current Health Sciences Journal. Jan-Mar2025, Vol. 51 Issue 1, p62-71. 10p.

Clinically Significant BRCA1 and BRCA2 Germline Variants in Breast Cancer—A Single-Center Experience.

Authors: Pleșea, Răzvan Mihail Riza, Anca-Lelia Ahmet, Ana Maria et al.

Source: Cancers. Jan2025, Vol. 17 Issue 1, p39. 20p.

Lack of Association Between BsmI and FokI Polymorphisms of the VDR Gene and Sporadic Colorectal Cancer in a Romanian Cohort—A Preliminary Study.

Authors: Petre-Mandache, Bianca Burada, Emilia Cucu, Mihai Gabriel et al.

Source: Current Oncology. Oct2024, Vol. 31 Issue 10, p6406-6418. 13p.

MMR Gene Expression Pattern in Sporadic Colorectal Cancer.

Authors: Ioana, Mihai Angelescu, Cristina Burada, Florin et al.

Source: Journal of Gastrointestinal & Liver Diseases. Jun2010, Vol. 19 Issue 2, p155-159. 5p. 1 Diagram, 4 Charts, 3 Graphs.

The Role of MLPA in Detecting Syndromic Submicroscopic Copy Number Variations in Normal QF-PCR Miscarriage Specimens.

Authors: Popescu-Hobeanu, Gabriela Cucu, Mihai-Gabriel Calotă-Dobrescu, Alexandru et al.

Source: Genes. Aug2025, Vol. 16 Issue 8, p867. 14p.

First Trimester Ultrasound Detection of Fetal Central Nervous System Anomalies.

Authors: Ungureanu, Delia Roxana Drăgușin, Roxana Cristina Căpitănescu, Răzvan Grigoraș et al.

Source: Brain Sciences (2076-3425). Jan2023, Vol. 13 Issue 1, p118. 18p.

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

Authors: Streață, Ioana Caramizaru, Alexandru Riza, Anca-Lelia et al.

Source: Diagnostics (2075-4418). Dec2022, Vol. 12 Issue 12, p3137. 16p.

Phenotype Heterogeneity in 3q29 Microduplication Syndrome.

Authors: STREATA, IOANA RIZA, ANCA-LELIA SOSOI, SIMONA et al.

Source: Current Health Sciences Journal. Apr-Jun2020, Vol. 46 Issue 2, p193-197. 5p.

miR-499a rs3746444 A>G Polymorphism Is Correlated with Type 2 Diabetes Mellitus and Diabetic Polyneuropathy in a Romanian Cohort: A Preliminary Study.

Authors: Burada, Emilia Roșu, Maria-Magdalena Sandu, Raluca Elena et al.

Source: Genes. Aug2023, Vol. 14 Issue 8, p1543. 11p.

Cytogenetic Analysis of Sporadic First-Trimester Miscarriage Specimens Using Karyotyping and QF-PCR: A Retrospective Romanian Cohort Study.

Authors: Popescu-Hobeanu, Gabriela Riza, Anca-Lelia Streață, Ioana et al.

Source: Genes. Dec2022, Vol. 13 Issue 12, p2246. 10p.

Terminal Deletion 2q37.3 in a Patient with Klippel-Trenaunay-Weber Syndrome.

Authors: Puiu, Ileana Stoica, Alin Sosoi, Simona et al.

Source: Fetal & Pediatric Pathology. Oct2013, Vol. 32 Issue 5, p351-356. 6p. 2 Black and White Photographs, 1 Graph.