Letter to Editor: The Feasibility and Acceptability of a Headache Self-Management Education Program for Adolescents [0.03%]
写给编辑的信：青少年头痛自我管理教育项目的可行性和接受度
Aradhana Chhabra,Riya Kalra,Kanu Goyal
Aradhana Chhabra
Incontinentia Pigmenti With Neonatal Encephalopathy: A Case Report and Literature Review [0.03%]
色素失禁症合并新生儿脑病：1例报告及文献复习
Hui Li,Adam Wallace,Chrysanthy Ikonomidou
Hui Li
BackgroundIncontinentia pigmenti (IP) is an X-linked neurocutaneous disorder caused by mutations in the IKBKG gene located at the Xq28 locus. This multisystem condition is primarily diagnosed based on 4 clinical criteria, including characte...
Diagnostic Strategies for Neuroblastoma in Children With Horner Syndrome: A Proposed Diagnostic Algorithm [0.03%]
儿童霍纳综合征神经母细胞瘤诊断策略：一种诊断算法的提议
Katarzyna Kuchalska,Anna Gotz-Więckowska,Walentyna Balwierz et al.
Katarzyna Kuchalska et al.
Neuroblastoma constitutes the most frequent solid tumor in children under 2 years of age. It is most often located in the abdomen; however, it may also be found in the mediastinum or the neck, and its first and only symptom may be Horner sy...
A Revealing Case of SHQ1-Related Neurodevelopmental Disorder: Expanding the Genotypic and Phenotypic Frontier [0.03%]
SHQ1相关神经发育障碍的一例揭示性病例：扩展基因型和表型界限
Emilee Ly,Marcus Lee
Emilee Ly
SHQ1-related neurodevelopmental disorder is a rare autosomal recessive condition linked to disrupted ribosome biogenesis, telomerase activity, and RNA modification. Among the few reported cases, typical clinical presentations consist of ear...
Counseling Preferences of Expectant Parents With a Fetal Neurologic Diagnosis: A Scoping Review of the Literature [0.03%]
胎儿神经性疾病孕妇家长的咨询倾向性：文献综述研究
Natalie K Field,Suepriya Adhikari,Saisha Dhar et al.
Natalie K Field et al.
Diagnosis and management of fetal neurologic conditions is evolving rapidly. This scoping review aims to synthesize existing literature characterizing parental preferences for fetal neurologic counseling. A literature search and screening o...
Mark Slater
Mark Slater
In this article, the author reflects on personal lived experience with epilepsy to explore the therapeutic value of historical context in epilepsy care. The experience of an epilepsy diagnosis is shaped not only by clinical realities, but b...
Fixel-Based Analysis of Pretreatment MRI Identifies White Matter Abnormalities in Pediatric Anti-NMDAR Encephalitis [0.03%]
基于固定点的术前MRI分析可识别儿科N-甲基-D天冬氨酸受体脑炎的白质异常现象
Daniel Ackom,Janine Taitt-Tap,Scott A Beardsley et al.
Daniel Ackom et al.
Anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis is an autoimmune disorder in which conventional MRI often appears normal, leading to clinical-radiologic dissociation and hindering early diagnosis and monitoring. We retrospectiv...
Physician Perception and Education Impact on Neurologic Treatment of People With Developmental Disabilities [0.03%]
医生的观念和教育对发育障碍患者神经治疗的影响
Joceline J Rodrigues,Mauricio F Villamar,Neishay Ayub et al.
Joceline J Rodrigues et al.
BackgroundPhysicians' attitudes toward individuals with developmental disabilities (DD) may be detrimental, with potential for misdiagnosis, mistreatment, avoidance of health care, and higher rates of illness.ObjectiveTo explore physician a...
Susan K Klein
Susan K Klein
Profound Biotinidase Deficiency as a Treatable Cause of Pediatric Diffuse Leukoencephalopathy and Diffusion Restriction [0.03%]
深生物素 idase 缺陷是儿科弥漫性脑白质病和弥散障碍的可治疗原因吗？
Soumya Jyoti Raha,Arushi Gahlot Saini,Savita Verma Attri et al.
Soumya Jyoti Raha et al.
BackgroundBiotinidase deficiency (BTD) is a rare, autosomal-recessive neurometabolic disorder due to biallelic pathogenic variants in the BTD gene. Diffuse leukoencephalopathy with diffusion restriction on neuroimaging is a rare but reversi...