日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Application of Eutectic-Solvent-Based Liquid–Liquid Microextraction for Removal of Eight Bisphenols from Water and Industrial Samples

基于共熔溶剂的液液微萃取法去除水和工业样品中的八种双酚类化合物的应用

Phillips, Robert A 3rd; Page, Stephanie C; Qu, Taimei; Tian, Lv; Nazarie, Florina Victoria; Dobrescu, Mihaela Amelia; Lazea, Cecilia; David, Ana Adriana; Șufană, Crina; Bucerzan, Simona; Cainap, Simona Sorana; Rancea, Raluca; Stănoiu-Pînzariu, Oana; Pascanu, Ionela Maria; Popp, Radu Anghel; Pop, Laura Ancuta; Lazăr, Călin; Alkhzouz, Camelia; Miclea, Diana; Vulturar, Romana; Adámek, Michal; Tůma, Petr; Bosáková, Zuzana

Clinical and Genetic Characterization of Noonan Syndrome in a Romanian Cohort from Transylvania: Details on PTPN11 c.922A>G Variant and Phenotypic Spectrum

来自特兰西瓦尼亚的罗马尼亚人群中努南综合征的临床和遗传特征:PTPN11 c.922A>G 变异和表型谱的详细信息

Nazarie, Florina Victoria; Miclea, Diana; Șufană, Crina; Botezatu, Alina; Popp, Radu Anghel; Pascanu, Ionela Maria; Alkhzouz, Camelia; Bucerzan, Simona; Lazăr, Călin; Lazea, Cecilia; Vulturar, Romana

Copy number variation analysis in 189 Romanian patients with global developmental delay/intellectual disability

对189名患有全面发育迟缓/智力障碍的罗马尼亚患者进行拷贝数变异分析

Miclea, Diana; Osan, Sergiu; Bucerzan, Simona; Stefan, Delia; Popp, Radu; Mager, Monica; Puiu, Maria; Zimbru, Cristian; Chirita-Emandi, Adela; Alkhzouz, Camelia

Molecular and Cytogenetic Analysis of Romanian Patients with Differences in Sex Development

对罗马尼亚性发育差异患者进行分子和细胞遗传学分析

Miclea, Diana; Alkhzouz, Camelia; Bucerzan, Simona; Grigorescu-Sido, Paula; Popp, Radu Anghel; Pascanu, Ionela Maria; Cret, Victoria; Ghervan, Cristina; Blaga, Ligia; Zaharie, Gabriela

46,XX DSD: Developmental, Clinical and Genetic Aspects

46,XX 性发育异常:发育、临床和遗传方面

Alkhzouz, Camelia; Bucerzan, Simona; Miclaus, Maria; Mirea, Andreea-Manuela; Miclea, Diana

Diagnostic Usefulness of MLPA Techniques for Recurrent Copy Number Variants Detection in Global Developmental Delay/Intellectual Disability

MLPA技术在全面发育迟缓/智力障碍中检测复发性拷贝数变异的诊断价值

Miclea, Diana; Szucs, Adriana; Mirea, Andreea; Stefan, Delia-Maria; Nazarie, Florina; Bucerzan, Simona; Lazea, Cecilia; Grama, Alina; Pop, Tudor Lucian; Farcas, Marius; Zaharie, Gabriela; Matyas, Melinda; Mager, Monica; Vintan, Mihaela; Popp, Radu; Alkhzouz, Camelia

Genetic testing in pediatric endocrine pathology

儿科内分泌病理学中的基因检测

Miclea, Diana; Alkhzouz, Camelia; Bucerzan, Simona; Grigorescu-Sido, Paula

Diagnostic, treatment and outcome possibilities in achondroplasia

软骨发育不全的诊断、治疗和预后可能性

Bucerzan, Simona; Alkhzouz, Camelia; Crisan, Mirela; Miclea, Diana; Asavoaie, Carmen; Ilies, Roxana; Grigorescu-Sido, Paula

Early clinical signs in lysosomal diseases

溶酶体疾病的早期临床症状

Alkhzouz, Camelia; Miclea, Diana; Bucerzan, Simona; Lazea, Cecilia; Nascu, Ioana; Sido, Paula Grigorescu

Cardiovascular manifestations in Marfan syndrome

马凡综合征的心血管表现

Lazea, Cecilia; Bucerzan, Simona; Crisan, Mirela; Al-Khzouz, Camelia; Miclea, Diana; Şufană, Crina; Cismaru, Gabriel; Grigorescu-Sido, Paula