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

Fetal genetic factors in pregnancy loss: Insights from a meta-analysis and effectiveness of whole exome sequencing

胎儿遗传因素与妊娠丢失:来自荟萃分析的启示及全外显子组测序的有效性

Hadjipanteli, Andrea; Theodosiou, Athina; Papaevripidou, Ioannis; Alexandrou, Angelos; Salameh, Nicole; Evangelidou, Paola; Tomazou, Marios; Mavrides, Andreas; Fasouliotis, Sozos; Anastasiou, George; Stavroulis, Andreas; Agathokleous, Niki; Agathokleous, Maria; Tsangarides, Stelios; Kallikas, Ioannis; Kakoullis, Kyriakos; Frakala, Sofia; Oxinou, Christina; Marnerides, Andreas; Athanasiou, Emilia; Ourani, Sofia; Anastasiadou, Violetta C; Tanteles, George; Kousoulidou, Ludmila; Sismani, Carolina

Sodium Channel Gene Variants in Fetuses with Abnormal Sonographic Findings: Expanding the Prenatal Phenotypic Spectrum of Sodium Channelopathies

胎儿超声检查异常与钠通道基因变异:拓展钠通道病产前表型谱

Hadjipanteli, Andrea; Theodosiou, Athina; Papaevripidou, Ioannis; Evangelidou, Paola; Alexandrou, Angelos; Salameh, Nicole; Kallikas, Ioannis; Kakoullis, Kyriakos; Frakala, Sofia; Oxinou, Christina; Marnerides, Andreas; Kousoulidou, Ludmila; Anastasiadou, Violetta C; Sismani, Carolina

Suspected twin anemia polycythemia sequence in a dichorionic, diamniotic twin pregnancy: a case report

疑似双绒毛膜双羊膜囊双胎妊娠合并双胎贫血-红细胞增多症序列:病例报告

Jeyaseelan, Tania; Shangaris, Panicos; Efthymiou, Athina; Martin, Linzi; Story, Lisa; Nanda, Surabhi; Gupta, Neelam; Al-Adnani, Mudher; Marnerides, Andreas; Nicolaides, Kypros H; Sankaran, Srividhya

Deep HDR Hallucination for Inverse Tone Mapping

用于反向色调映射的深度HDR幻觉

Marnerides, Demetris; Bashford-Rogers, Thomas; Debattista, Kurt

Placental magnetic resonance imaging in chronic hypertension: A case-control study

慢性高血压患者胎盘磁共振成像:一项病例对照研究

Ho, Alison; Hutter, Jana; Slator, Paddy; Jackson, Laurence; Seed, Paul T; Mccabe, Laura; Al-Adnani, Mudher; Marnerides, Andreas; George, Simi; Story, Lisa; Hajnal, Joseph V; Rutherford, Mary; Chappell, Lucy C

A hemizygous mutation in the FOXP3 gene (IPEX syndrome) resulting in recurrent X-linked fetal hydrops: a case report

FOXP3基因半合子突变(IPEX综合征)导致复发性X连锁胎儿水肿:病例报告

Shangaris, Panicos; Ho, Alison; Marnerides, Andreas; George, Simi; AlAdnani, Mudher; Yau, Shu; Jansson, Mattias; Hoyle, Jacqueline; Ahn, Joo Wook; Ellard, Sian; Irving, Melita; Wellesley, Diana; Pasupathy, Dharmintra; Holder-Espinasse, Muriel

Post-mortem Characterisation of a Case With an ACTG1 Variant, Agenesis of the Corpus Callosum and Neuronal Heterotopia

对一例携带ACTG1变异、胼胝体发育不全和神经元异位症的病例进行尸检特征分析

Vontell, Regina; Supramaniam, Veena G; Davidson, Alice; Thornton, Claire; Marnerides, Andreas; Holder-Espinasse, Muriel; Lillis, Suzanne; Yau, Shu; Jansson, Mattias; Hagberg, Henrik E; Rutherford, Mary A