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

Neurological diagnoses in children potentially fulfilling the criteria for developmental coordination disorder

儿童神经系统诊断可能符合发育性协调障碍的诊断标准

Garofalo, Martinica; Vansenne, Fleur; van Hoorn, Jessika F; Tijssen, Marina A J; Verbeek, Dineke S; Sival, Deborah A

Screening Tool Improves Recognition of Movement Disorders by Internists and Paediatricians in Patients With Inherited Metabolic Diseases

筛查工具可提高内科医生和儿科医生对遗传性代谢疾病患者运动障碍的识别率

Hulshof, Ellen M; Lantinga, Hugo P; Alkemade, Gonnie; Bosch, Annet M; Brands, Marion M; Vliet, Danique Draaisma-van; Haijer-Schreuder, Andrea B; Hoytema van Konijnenburg, Eva M M; Janssen, Mirian C H; van der Klauw, Melanie M; Langeveld, Mirjam; Lubout, Charlotte M A; van Ockenburg, Sonja L; Oussoren, Esmeralda; Panis, Bianca; Sjouke, Barbara; de Vries, Maaike; Wagenmakers, Margreet A E M; Wijnen, Mark; Sival, Deborah A; Tijssen, Marina A J; de Koning, Tom J; Koens, Lisette H

Genetic Insights in Hindbrain Abnormalities Through Network Analysis Expose Key Biological Pathways in Hindbrain Development

通过网络分析揭示后脑异常的遗传学见解,揭示后脑发育的关键生物学通路

van Noort, Suus A M; Sival, Deborah A; Verbeek, Dineke S

Do not Forget to Measure the Head: Hydrocephalus Can Phenotypically Mimic Developmental Coordination Disorder

别忘了测量头围:脑积水在表型上可能与发育性协调障碍相似

Garofalo, Martinica; Helfferich, Jelte; Kloet, Reina W; Sival, Deborah A; Heineman, Kirsten R

Absence of Pupillary Reflexes in Pediatric Acute Liver Failure and Neurological Outcome After Liver Transplantation

儿童急性肝衰竭患者瞳孔反射消失与肝移植术后神经系统预后的关系

Schouwstra, Kirsten J; Scheenstra, René; de Kleine, Ruben H; de Meijer, Vincent E; Bontemps, Sander T H; Verkade, Henkjan J; Sival, Deborah A

Neurologic Outcome Comparison between Fetal Open-, Endoscopic- and Neonatal-Intervention Techniques in Spina Bifida Aperta

胎儿开放手术、内镜手术和新生儿介入治疗开放性脊柱裂的神经系统结局比较

Sival, Deborah A; Patuszka, Agnieszka; Koszutski, Tomasz; Heep, Axel; Verbeek, Renate J

Pathogenetic Insights into Developmental Coordination Disorder Reveal Substantial Overlap with Movement Disorders

发育性协调障碍的发病机制研究揭示其与运动障碍存在显著重叠

Garofalo, Martinica; Vansenne, Fleur; Sival, Deborah A; Verbeek, Dineke S

2D Gait Skeleton Data Normalization for Quantitative Assessment of Movement Disorders from Freehand Single Camera Video Recordings

基于自由手持单摄像头视频记录的二维步态骨骼数据标准化方法,用于运动障碍的定量评估

Tang, Wei; van Ooijen, Peter M A; Sival, Deborah A; Maurits, Natasha M

The ARCA Registry: A Collaborative Global Platform for Advancing Trial Readiness in Autosomal Recessive Cerebellar Ataxias

ARCA注册库:推进常染色体隐性小脑共济失调临床试验准备工作的全球合作平台

Traschütz, Andreas; Reich, Selina; Adarmes, Astrid D; Anheim, Mathieu; Ashrafi, Mahmoud Reza; Baets, Jonathan; Basak, A Nazli; Bertini, Enrico; Brais, Bernard; Gagnon, Cynthia; Gburek-Augustat, Janina; Hanagasi, Hasmet A; Heinzmann, Anna; Horvath, Rita; de Jonghe, Peter; Kamm, Christoph; Klivenyi, Peter; Klopstock, Thomas; Minnerop, Martina; Münchau, Alexander; Renaud, Mathilde; Roxburgh, Richard H; Santorelli, Filippo M; Schirinzi, Tommaso; Sival, Deborah A; Timmann, Dagmar; Vielhaber, Stefan; Wallner, Michael; van de Warrenburg, Bart P; Zanni, Ginevra; Zuchner, Stephan; Klockgether, Thomas; Schüle, Rebecca; Schöls, Ludger; Synofzik, Matthis

De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disability

CAMTA1基因的新生突变会导致一种综合征,该综合征的症状与痉挛、共济失调和智力障碍的关联程度不一。

Wijnen, Iris G M; Veenstra-Knol, Hermine E; Vansenne, Fleur; Gerkes, Erica H; de Koning, Tom; Vos, Yvonne J; Tijssen, Marina A J; Sival, Deborah; Darin, Niklas; Vanhoutte, Els K; Oosterloo, Mayke; Pennings, Maartje; van de Warrenburg, Bart P; Kamsteeg, Erik-Jan