Sleep Problems in Children With Autism and Other Developmental Disabilities: A Brief Report [0.03%]
孤独症及其他发育障碍儿童的睡眠问题-简报报告
Maria Valicenti-McDermott,Katharine Lawson,Kathryn Hottinger et al.
Maria Valicenti-McDermott et al.
Sleep problems in children with autism and the association with child behavioral problems was studied in an ethnically diverse population, in a cross-sectional study with structured interview. Sample included 50 families of children with au...
When an Early Diagnosis of Autism Spectrum Disorder Resolves, What Remains? [0.03%]
自闭症谱系障碍早期诊断消失后还剩什么？
Lisa Shulman,Erin D&#x;Agostino,Samantha Lee et al.
Lisa Shulman et al.
A chart review was performed of 38 children diagnosed with autism spectrum disorder (ASD) by 3 years of age at an inner-city developmental program who subsequently experienced resolution of ASD symptomatology and no longer met diagnostic cr...
Unusual Presentation of PMM2-Congenital Disorder of Glycosylation With Isolated Strokelike Episodes in a Young Girl [0.03%]
PMM2-锥体外系糖蛋白合成障碍伴孤立性脑卒中样发作的特殊表现形式-一例年轻女性患者报告
Rajni Farmania,Puneet Jain,Suvasini Sharma et al.
Rajni Farmania et al.
Congenital disorders of glycosylation (CDG) are multisystemic inherited metabolic disorders with marked phenotypic variability. The most frequent described type is PMM2-CDG (earlier known as CDG Type Ia) which presents either with pure neur...
Usefulness of Cerebral Palsy Curves in Mexican Patients: A Cross-Sectional Study [0.03%]
墨西哥脑瘫患者生长曲线的适用性研究：横断面研究
Carlos P Viñals-Labañino,Ana E Velazquez-Bustamante,Silvia I Vargas-Santiago et al.
Carlos P Viñals-Labañino et al.
Cerebral palsy describes a group of movement and posture disorders that cause activity limitation, and are attributable to nonprogressive disorders that occur in the fetal or infant brain. The growth of these children should not be compared...
Observational Study
Journal of child neurology. 2019 May;34(6):332-338. DOI:10.1177/0883073819830560 2019
Functional Neurologic Symptom Disorder in Children: Clinical Features, Diagnostic Investigations, and Outcomes at a Tertiary Care Children's Hospital [0.03%]
儿童功能神经症状障碍的临床特征、诊断检查和预后——一家三级护理儿童医院的经验
Carla Watson,Lalitha Sivaswamy,Roshani Agarwal et al.
Carla Watson et al.
Objective: To describe the presenting symptoms and short-term outcomes of children diagnosed with functional neurologic symptom disorder and to compare the demographic and clinical characteristics of children who received...
Botulinum Toxins Type A (Bont-A) in the Management of Lower Limb Spasticity in Children: A Systematic Literature Review and Bayesian Network Meta-analysis [0.03%]
儿童下肢肌张力障碍管理中肉毒杆菌毒素A型(BONT-A)的文献系统回顾和贝叶斯网络meta分析
Patricia Guyot,Chrysostomos Kalyvas,Carole Mamane et al.
Patricia Guyot et al.
Background: Botulinum neurotoxins type A (BoNT-As) are used in pediatric lower limb spasticity, which affects more than 2.5 million children worldwide. Botulinum neurotoxins type-A improve active function and delay muscul...
A Proof-of-Principle, Case-Control Study to Compensate for Potential Carbohydrates in Liquid Antiseizure Drugs in Children on the Ketogenic Diet [0.03%]
一项验证原理的病例对照研究：评估儿童在服用液体制抗癫痫药物时潜在碳水化合物的影响 ketogenic diet ketogenic饮食）
Courtney A Haney,Anita Charpentier,Zahava Turner et al.
Courtney A Haney et al.
Introduction: Since its creation, patients on ketogenic diet are told to avoid liquid medications due to theoretical concerns of "hidden" carbohydrates. However, switching from liquid to tablet formulations can be problem...
Senem Ayça,Halil Ural Aksoy,İsmail Taştan et al.
Senem Ayça et al.
Levels of melatonin have been reported before in children with epilepsy, but such has not been reported to date in those with continuous spikes and waves during sleep. The aim of the present study was to assess serum melatonin levels and me...
Stormorken Syndrome: A Rare Cause of Myopathy With Tubular Aggregates and Dystrophic Features [0.03%]
风暴恩综合征：肌管聚集物肌病伴进行性肌营养不良特征的罕见原因
Ang Li,Xuan Kang,Frederick Edelman et al.
Ang Li et al.
Stormorken syndrome is a rare genetic disorder (MIM 185070) first reported in 1983 with thrombocytopenia, muscle weakness, asplenia, and miosis caused by a mutation of the stromal interaction molecule 1 ( STIM1) gene.1 The muscle weakness i...
Combined Conventional and Amplitude-Integrated EEG Monitoring in Neonates: A Prospective Study [0.03%]
结合常规监测和振幅整合脑电图监测在新生儿中的应用：一项前瞻性研究
Sarah Grace Buttle,Brigitte Lemyre,Erick Sell et al.
Sarah Grace Buttle et al.
Background/objective: Seizure monitoring via amplitude-integrated EEG is standard of care in many neonatal intensive care units; however, conventional EEG is the gold standard for seizure detection. We compared the diagno...