Spatial and Temporal Analysis of Hospital Discharges due to Congenital Malformations in Argentina [0.03%]
阿根廷先天畸形住院治疗的时空分析
Marcelo I Figueroa,Lautaro D Andrade,Jorge S López-Camelo et al.
Marcelo I Figueroa et al.
Background: Hospital discharges (HD) provide population data that can be used to define specific epidemiological profiles. Objectives: ...
FGFR1 Tyrosine Kinase Domain Variant p.Val561Met in Caudal Dysraphism: A Case Report [0.03%]
尾部脊柱裂中成纤维细胞生长因子受体1酪氨酸激酶结构域变异p.Val561Met一例报告
Himanshu Goel,Victoria Yachmenikova,Tanya Mckenny et al.
Himanshu Goel et al.
Background: Neural tube defects (NTDs) are complex congenital malformations with both environmental and genetic contributions. Monogenic causes of NTDs are increasingly recognized, particularly those involving genes that ...
Case Reports
Birth defects research. 2025 Nov;117(11):e70000. DOI:10.1002/bdr2.70000 2025
Effects of Pre-Conception Stress and Dracocephalum moldavica Extract on Sperm Parameters and Sex Hormones in Parents and Offspring [0.03%]
孕前应激和毛蕊藁提取物对父母及子代精子参数和性激素的影响
Leila Ghassemifard,Hajar Ramezanikhah,Parisa Jafari et al.
Leila Ghassemifard et al.
Background: Stress is one of the causes of fertility weakness in both females and males and herbal approaches may reduce this harmful effect. This study aimed to investigate the effect of Dracocephalum moldavica (DM) on t...
Understanding Clubfoot: Integrating Historical Origins, Embryologic Foundations, Epidemiology and Etiology-A Review [0.03%]
先天性clubfoot的历史沿革、发生学基础、流行病学及病因机制研究进展——综述文章
J S R G Saran,Varun Devdass,Durai Anand
J S R G Saran
Purpose: Congenital talipes equinovarus (CTEV) or idiopathic clubfoot, is a common yet complex congenital musculoskeletal deformity characterized by cavus, adductus, varus and equinus components. Despite advances in conse...
Pregnancy Outcomes Following Paternal Methotrexate Exposure: A Systematic Review and Meta-Analysis [0.03%]
父亲接触甲氨蝶呤后的妊娠结局：系统评价和荟萃分析
Nusret Uysal,Hüseyin Yilmaz,Mesut Gungor et al.
Nusret Uysal et al.
Objective: Evidence guiding the management of pregnancies fathered by men exposed to methotrexate (MTX) remains limited. This systematic review and meta-analysis evaluated whether paternal MTX exposure before or at concep...
Infant Mortality due to Congenital Diaphragmatic Hernia, United States 2007-2021 [0.03%]
2007年至2021年美国因先天性膈疝导致的婴儿死亡率
Ramesh Vidavalur,Kanekal S Gautham
Ramesh Vidavalur
Objective: To analyze temporal trends and geographic variations in infant mortality rate associated with congenital diaphragmatic hernia (CDH-IMR) in the United States. ...
Expression Pattern Alterations of the Brain KCC2 Chloride Transporter in Male Rats Following Postnatal Extremely Low-Frequency Electromagnetic Field Exposure Associated With Behavioral Outcomes [0.03%]
极低频电磁场暴露对雄性大鼠脑KCC2氯通道表达及行为学影响的研究
Mozhdeh Nemati,Masoumeh Nozari,Fatemeh Darvishzadeh-Mahani et al.
Mozhdeh Nemati et al.
Background: Exposure to extremely low-frequency magnetic fields (ELF-MFs) has increased with technological development. Environmental factors are known to influence the K+-Cl- cotransporter 2 (KCC2), which regulates neuro...
Maternal Immune Stimulation With Interferon-Gamma Limits Embryonic Valproic Acid Induced Apoptotic Gene Expression [0.03%]
干扰素-γ刺激限制母体瓦尔帕拉依索酸诱导的胚胎细胞凋亡基因表达
Daniel Frascella,Murali K Mallela,Robert Cullen et al.
Daniel Frascella et al.
Background: Neural tube defects (NTDs) are developmental malformations affecting 1300 newborns in the United States each year. Valproic acid (VA), a drug to treat seizures and mood disorders, can cause NTDs. Apoptosis is ...
Maternal and Placental Inflammation Influence Formation of Neural Tube Defects in Quaternary Ammonium Compound Exposed Mice [0.03%]
季铵化合物致小鼠神经管缺陷与母体及胎盘炎症反应的关系研究
Justin Kula,Ryan P Seguin,Libin Xu et al.
Justin Kula et al.
Background: Quaternary ammonium compounds (QACs) are common chemicals used for their antimicrobial, antistatic, and surfactant properties. Two common QACs, alkyldimethylbenzyl ammonium chloride (ADBAC or BAC) and didecyld...
A Case Report: Co-Occurrence of TNRC6B Gene Variant and Xq28 Microdeletion Syndrome With Comprehensive Literature Review [0.03%]
病例报告及文献综述：TNRC6B基因突变和Xq28微缺失综合征共病研究
Ying Deng,Chenchen Bu,Zhuoma Basang et al.
Ying Deng et al.
Background: TNRC6B encodes a protein crucial for RNA silencing, and heterozygous variants of TNRC6B have been associated with developmental delay/intellectual disability, speech and language delay, fine and motor delay, a...