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Child Neurology Open

中文名称：儿童神经病学开放

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1.A Rare Syndrome of GRID2 Deletion in 2 Siblings:

机译：2个兄弟姐妹中GRID2缺失的罕见综合征：
- 作者：Aravindhan Veerapandiyan;Stephanie Enner;Venkatraman Thulasi;Xue Ming
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- Glutamate receptorionotropicdelta 2ataxiadevelopmental delaytonic upgaze;
2.Two Novel KCNQ2 Mutations in 2 Families With Benign Familial Neonatal Convulsions:

机译：在两个具有良性家族性新生儿惊厥的家庭中的两个新型KCNQ2突变：
- 作者：Ghalia Al Yazidi;Michael I. Shevell;Myriam Srour
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- benign familial neonatal convulsionsBFNCKCNQ2;
3.Evidence of the Effectiveness of Primary Brachial Plexus Surgery in Infants With Obstetric Brachial Plexus Palsya??Revisited:

机译：婴幼儿臂丛神经原发性臂丛神经外科手术有效性的证据？
- 作者：Amel A. F. El-Sayed
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- Erba??s palsybrachial plexusprimary surgeryconservative management;
4.The Effect of Noninvasive Positive Pressure Ventilation on Pneumonia Hospitalizations in Children With Neurological Disease:

机译：无创正压通气对神经病患儿肺炎住院的影响：
- 作者：Abeyat Zaman-Haque;Craig Campbell;Dhenuka Radhakrishnan
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- noninvasive ventilationneurologic diseaserespiratory failurepneumonianeuromuscular disease;
5.Temporary Efficacy of Pyrimethamine in Juvenile-Onset Tay-Sachs Disease Caused by 2 Unreported HEXA Mutations in the Indian Population:

机译：乙胺嘧啶在印度裔人群中由2种未报告的HEXA突变引起的青少年性Tay-Sachs病的暂时疗效：
- 作者：Anaita Udwadia-Hegde;Omkar Hajirnis
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- juvenile Tay-Sachs diseasehexosaminidase Acompound heterozygouspyrimethamineIndia;
6.Novel SCN1A and GABRA1 Gene Mutations With Diverse Phenotypic Features and the Question on the Existence of a Broader Spectrum of Dravet Syndrome:

机译：具有不同表型特征的新型SCN1A和GABRA1基因突变以及关于Dravet综合征更广谱存在的问题：
- 作者：Maria P. Gontika;Christopher Konialis;Constantine Pangalos;Antigone Papavasiliou
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- epileptic encephalopathyinfantgeneticsmutationnext generation sequencing;
7.CEDNIK: Phenotypic and Molecular Characterization of an Additional Patient and Review of the Literature

机译：CEDNIK：另一位患者的表型和分子特征以及文献复习
- 作者：Tina Hsu;Carrie C. Coughlin;Kristin G. Monaghan;Elise Fiala;Robert C. McKinstry;Alex R. Paciorkowski;Marwan Shinawi
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- CEDNIKdevelopmental delayichthyosispolymicrogyriaSNAP29;
8.Maternal Racea??Ethnicity, Immigrant Status, Country of Birth, and the Odds of a Child With Autism:

机译：孕产妇种族，种族，移民身份，出生国家和自闭症儿童的几率：
- 作者：Jenny Fairthorne;Nick de Klerk;Helen M. Leonard;Laura A. Schieve;Marshalyn Yeargin-Allsopp
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- autismdevelopmental disabilityepidemiologyimmigrantintellectual disabilityrace;
9.Implementing a Multidisciplinary Approach to Treating Tuberous Sclerosis Complex: A Case Report

机译：实施多学科方法治疗结节性硬化症：一例报告
- 作者：Tanjala T. Gipson;Andrea Poretti
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- tuberous sclerosis complexseizuresneuroimagingpediatricbehaviorbrain tumor;
10.A Case of Brown-Vialetto-Van Laere Syndrome Due To a Novel Mutation in SLC52A3 Gene: Clinical Course and Response to Riboflavin

机译：SLC52A3基因新型突变引起的布朗-维亚莱托-范·莱尔综合症一例：临床过程和对核黄素的反应
- 作者：Venkatraman Thulasi;Aravindhan Veerapandiyan;Beth A. Pletcher;Chun M. Tong;Xue Ming
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- riboflavin transporter deficiencyBrown-Vialetto-Van Laere syndromeSLC52A3pontobulbar palsyataxia;
11.Visceral Hyperalgesia: When to Consider Gabapentin Use in Neonatesa??Case Study and Review

机译：内脏痛觉过敏：何时在新生儿中考虑使用加巴喷丁？
- 作者：Joseph Asaro;Christine A. Robinson;Philip T. Levy
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- gabapentinvisceral hyperalgesianeonatesneuropathic pain;
12.X-Linked Lissencephaly With Absent Corpus Callosum and Abnormal Genitalia: An Evolving Multisystem Syndrome With Severe Congenital Intestinal Diarrhea Disease

机译：X联性缺脑症与Corp体缺席和生殖器异常：严重的先天性肠道腹泻病的演变的多系统综合征。
- 作者：David Coman;Tom Fullston;Cheryl Shoubridge;Richard Leventer;Flora Wong;Simon Nazaretian;Ian Simpson;Josef Gecz;George McGillivray
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- XLAGlissencephalyagenesis of the corpus callosumdiarrheapancreatic insufficiencyenteroendocrine cellsARX genecongenital intestinal diarrheal diseases;
13.Psychological Assessment of Patients With Biotin-Thiamine-Responsive Basal Ganglia Disease:

机译：生物素-硫胺素反应性基底节病患者的心理评估：
- 作者：Majid Alfadhel;Amal Al-Bluwi
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- biotin-thiamine-responsive basal ganglia diseasebiotin-responsive basal ganglia diseasethiaminebiotinpsychological assessment;
14.Performance Monitoring in Children Following Traumatic Brain Injury Compared to Typically Developing Children:

机译：与典型发育中的儿童相比，创伤性脑损伤儿童的表现监测：
- 作者：Amy A. Wilkinson;Maureen Dennis;Margot J. Taylor;Anne-Marie Guerguerian;Kathy Boutis;Karen Choong;Craig Campbell;Douglas Fraser;Jamie Hutchison;Russell Schachar;for the Canadian Critical Care Trials Group (CCCTG)
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- performance monitoringstop-signal tasktraumatic brain injurypediatrics;
15.Phenotypic Heterogeneity of the m.14459GA Mutation:

机译：m.14459G> A突变的表型异质性：
- 作者：Josef Finsterer;Sinda Zarrouk-Mahjoub
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- mitochondrialmtDNAphenotypegenotypefracturesosteoporosis;
16.Symptomatic Neonatal Arterial Ischemic Stroke With Prenatal and Postnatal Neuroimaging:

机译：有症状的新生儿动脉缺血性卒中伴产前和产后神经影像学检查：
- 作者：Mati Pulver;Kristiina Juhkami;Dagmar Loorits;Pilvi Ilves;Jaanika Kuld;Eve ??iglane-??lik;Tuuli Metsvaht;Rael Laugesaar
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- strokemagnetic resonance imagingneuroimagingneonatal seizuresseizure;
17.Effect of Menstrual Cycle on Acute Intermittent Porphyria:

机译：月经周期对急性间歇性卟啉症的影响：
- 作者：V. R. Souza J?onior;V. M. V. Lemos;I. M. L. Feitosa;R. Florencio;C. W. B. Correia;L. B. Correia Fontes;M. F. Hazin Costa;M. C. B. Correia
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- acute intermittent porphyriaanxietyhyponatremiabehaviorpediatric;
18.Hyperostosis Frontalis Interna in a Child With Severe Traumatic Brain Injury:

机译：一名患有严重颅脑外伤的儿童的额骨额叶增生症：
- 作者：Yaxiong Li;Xin Wang;Yan Li
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- hyperostosisbenign bone lesionsfrontal bonechildbrain trauma;
19.Epileptic Negative Myoclonus as the First and Only Symptom in a Challenging Diagnosis of Benign Epilepsy With Centrotemporal Spikes:

机译：癫痫性阴性肌阵挛是具有挑战性的中央颞尖刺癫痫诊断的第一个也是唯一的症状：
- 作者：Jing Chen;Guo Zheng;Hu Guo;Xiaopeng Lu;Chunfeng Wu;Xiaoyu Wang;Wei Tao
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- epileptic negative myoclonusbenign epilepsy with centrotemporal spikesVEEGsurface EEG;
20.PRUNE Syndrome Is a New Neurodevelopmental Disorder: Report and Review

机译：PRUNE综合征是一种新的神经发育障碍：报告和审查
- 作者：Majid Alfadhel;Marwan Nashabat;Khalid Hundallah;Amal Al Hashem;Ahmed Alrumayyan;Brahim Tabarki
- 期刊名称：《Child Neurology Open》 | 2018年第2期
- PRUNE syndromePRUNE1progressive microcephalyspasticitydevelopmental delay;
21.Therapeutic Effect of Steroids in Osmotic Demyelination of Infancy:

机译：类固醇对婴儿渗透性脱髓鞘的治疗作用：
- 作者：Lalit R. Bansal
- 期刊名称：《Child Neurology Open》 | 2018年第2期
- central pontine myelinolysisextrapontine myelinolysismethylprednisolone;
22.Spinal Muscular Atrophy With Respiratory Distress Type 1a??A Child With Atypical Presentation:

机译：患有1a型呼吸窘迫的脊髓性肌萎缩症-非典型表现的儿童：
- 作者：Annie Ting Gee Chiu;Sophelia Hoi Shan Chan;Shun Ping Wu;Shun Hin Ting;Brian Hon Yin Chung;Angel On Kei Chan;Virginia Chun Nei Wong
- 期刊名称：《Child Neurology Open》 | 2018年第2期
- SMARD1IGHMBP2 genecongenital heart diseaseneuropathychildren;
23.Acute Transverse Myelitis Caused by Echovirus 11 in a Pediatric Patient: Case Report and Review of the Current Literature

机译：小儿患者中由Echovirus 11引起的急性横贯性脊髓炎：病例报告和当前文献复习
- 作者：Heidi L. Moline;Peter I. Karachunski;Anna Strain;Jayne Griffith;Cynthia Kenyon;Mark R. Schleiss
- 期刊名称：《Child Neurology Open》 | 2018年第2期
- encephalitisepidemiologymagnetic resonance imagingMRIpediatricenterovirusacute flaccid myelitisviral meningoencephalitis;
24.Intracranial Hemorrhage and Autoimmune Thrombocytopenia in a Neonate: A Rare a??Unpredictablea?? Event

机译：新生儿颅内出血和自身免疫性血小板减少症：罕见的“不可预测的”事件
- 作者：Andrea Becocci;Cristina Felice-Civitillo;M??ryle Laurent;Fran?§oise Boehlen;Roberta De Luca;Joel Fluss
- 期刊名称：《Child Neurology Open》 | 2018年第2期
- autoimmunebrainmagnetic resonance imagingneonatal seizuresneonateneuroimagingseizures;
25.De Novo KCNQ2 Mutation in One Case of Epilepsy of Infancy With Migrating Focal Seizures That Evolved to Infantile Spasms:

机译：De Novo KCNQ2突变在1例婴儿期癫痫伴转移性癫痫发作演变成小儿痉挛的情况下：
- 作者：Haolin Duan;Jing Peng;Miriam Kessi;Fei Yin
- 期刊名称：《Child Neurology Open》 | 2018年第2期
- KCNQ2 gene mutationepilepsy of infancy with migrating focal seizuresinfantile spasms.;
26.Use of Cyclophosphamide in a Child With Fulminant Acute Disseminated Encephalomyelitis:

机译：环磷酰胺在儿童急性急性弥漫性脑脊髓炎中的应用：
- 作者：Hana Ayed;Mohammed W. Chaudhary;Raidah AlBaradie;Ali Mir
- 期刊名称：《Child Neurology Open》 | 2018年第2期
- fulminant ADEMacute disseminated encephalomyelitiscyclophosphamideplasmapheresismethylprednisolone;
27.Childhood-Onset Progressive Dystonia With Mitochondrial DNA G14459A Mutation: Efficacy of Long-Term Sodium Succinate Treatment

机译：线粒体DNA G14459A突变的儿童发作性肌张力障碍：长期琥珀酸钠治疗的功效。
- 作者：Ayaka Koide;Hiroshi Ozawa;Masaya Kubota;Yuichi Goto
- 期刊名称：《Child Neurology Open》 | 2014年第1期
- mitochondrial DNALeber hereditary optic neuropathydystonia;
28.Neuro-Beh?§ets in a Child:

机译：儿童的神经行为：
- 作者：Zachary A. Vesoulis;Rafael Galindo;Bradley W. Ornstein;Andrew J. White
- 期刊名称：《Child Neurology Open》 | 2014年第1期
- MRIuveitisvitritispapillitishypertoniaincontinenceurinary tract infectionazathioprine;
29.Brave New World:

机译：美丽新世界：
- 作者：Marc C. Patterson
- 期刊名称：《Child Neurology Open》 | 2014年第1期
30.A Case Report of Homocystinuria With Dystonia and Stroke:

机译：同型肌尿症伴肌张力障碍和中风的一例报告：
- 作者：Arezoo Rezazadeh;Shahram Oveisgharan;Gholamali Shahidi;Reza Naghdi
- 期刊名称：《Child Neurology Open》 | 2014年第1期
- homocysteinemovement disordercerebrovascular disease;
31.Connexin 43 and Its Hemichannels Mediate Hypoxiaa??Ischemia-Induced Cell Death in Neonatal Rats:

机译：连接蛋白43及其半通道介导新生大鼠低氧血症缺血诱导的细胞死亡：
- 作者：Jingwei Wang;Aihua Ma;Jiashui Xi;Yulin Wang;Bojun Zhao
- 期刊名称：《Child Neurology Open》 | 2014年第1期
- connexin 43gap junction hemichannelastrocyteshypoxiaa??ischemia (HI)oxygena??glucose deprivation (OGD)neuroprotection;
32.Anterior Commissure Involvement in Humanherpes Virus 6 Encephalitis:

机译：人带疱疹病毒6型脑炎的前连合参与：
- 作者：Katsunori Fujii;Hajime Ikehara;Koo Nagasawa;Haruka Hishiki;Hideki Uchikawa;Naoki Shimojo
- 期刊名称：《Child Neurology Open》 | 2014年第1期
- connecting fiberhuman herpesvirus 6magnetic resonance imagingcytotoxic edema;
33.A Novel 1.0 Mb Duplication of Chromosome 8p22-21.3 in a Patient With Autism Spectrum Disorder:

机译：自闭症谱系障碍患者中染色体8p22-21.3的新型1.0 Mb复制：
- 作者：Ping Dong;Qiong Xu;Yu An;Bing-Rui Zhou;Ping Lu;Ren-Chao Liu;Xiu Xu
- 期刊名称：《Child Neurology Open》 | 2015年第2期
- autism spectrum disorderarray-comparative genomic hybridizationchromosome 8p22-21.3;
34.Is Chromosome 15q13.3 Duplication Involving CHRNA7 Associated With Oral Clefts?:

机译：涉及CHRNA7的15q13.3染色体重复与口腔裂痕相关吗？
- 作者：Yingjun Xie
- 期刊名称：《Child Neurology Open》 | 2015年第4期
- autism15q13.3 microduplicationCMA-SNP arrayCHRNA7oral clefts;
35.Clinical Phenotype of De Novo GNAO1 Mutation: Case Report and Review of Literature

机译：De Novo GNAO1突变的临床表型：病例报告和文献复习
- 作者：Inga Talvik;Rikke S. M??ller;Merilin Vaher;Ulvi Vaher;Line HG Larsen;Hans A. Dahl;Pilvi Ilves;Tiina Talvik
- 期刊名称：《Child Neurology Open》 | 2015年第2期
- early infantile epileptic encephalopathyohtahara syndromeGNAO1 mutationnext generation sequencing gene panel;
36.Use of Magnesium Sulfate Infusion for the Management of Febrile Illness-Related Epilepsy Syndrome: A Case Series

机译：硫酸镁输注治疗高热疾病相关性癫痫综合征的应用：病例系列
- 作者：Wei Wei Tan;Derrick W. S. Chan;Jan Hau Lee;Terrence Thomas;Anuradha P. Menon;Yoke Hwee Chan
- 期刊名称：《Child Neurology Open》 | 2015年第1期
- febrile illness-related epilepsy syndromerefractory status epilepticusmagnesium sulfate infusion;
37.Assessing Children With Disabilities Using WHO International Classification of Functioning, Disability and Health Child and Youth Version Activities and Participation D Codes:

机译：使用WHO国际功能，残疾与健康国际分类儿童和青少年版活动和参与D代码对残疾儿童进行评估：
- 作者：Niels Ove Illum;Kim Oren Gradel
- 期刊名称：《Child Neurology Open》 | 2015年第4期
- childhood disabilityInternational Classification of FunctioningDisabilityHealth childyouth versiond codespsychometricsRasch data analysis;
38.Newly Identified Characteristics and Suggestions for Diagnosis and Treatment of Diffuse Leptomeningeal Glioneuronal/Neuroepithelial Tumors: A Case Report and Review of the Literature

机译：弥漫性软脑膜神经胶质神经/神经上皮肿瘤的新发现特征及诊治建议：一例并文献复习
- 作者：Megan R. Lyle;Jaydevsinh N. Dolia;Jonathan Fratkin;Todd A. Nichols;Betty L. Herrington
- 期刊名称：《Child Neurology Open》 | 2015年第1期
- diffuse leptomeningeal enhancementintraparenchymal cystsleptomeningeal glioneuronal tumorneuroepithelial tumor;
39.Spontaneous Malignant Transformation of a Pilocytic Astrocytoma of Cerebellum: Case Report

机译：小脑星形星形细胞瘤的自发恶性转化：病例报告
- 作者：Joana Coelho;Sofia Nunes;Duarte Salgado
- 期刊名称：《Child Neurology Open》 | 2015年第1期
- low-grade gliomaspilocytic astrocytomamalignant transformation;
40.Guillain Barr?? Syndrome in a Child With X-Linked Adrenoleukodystrophy:

机译：格林·巴尔（Guillain Barr）？ X联肾上腺皮质营养不良儿童的综合症：
- 作者：Ron Jacob;Hanna Mandel;Naim Shehadeh
- 期刊名称：《Child Neurology Open》 | 2015年第4期
- pediatricneurologyautoimmuneAddisona??s disease;
41.A New Observation of an Atypical and Severe Variant of the Guillain-Barre Syndrome in a Child: Remaining Challenges for Diagnosis, Nosologic Classification, and Therapeutic Course

机译：儿童吉兰-巴雷综合征的非典型和严重变异的新观察：诊断，疾病分类和治疗过程仍面临挑战
- 作者：Linda Pons;V??ronique Manel;Doroth??e Ville;Etienne Javouhey;Fabienne Bordet
- 期刊名称：《Child Neurology Open》 | 2015年第4期
- Guillain-Barr?? syndromepediatricsMycoplasma pneumonia;
42.Encephalocraniocutaneous Lipomatosis: A Rare Association With Tethered Spinal Cord Syndrome With Review of Literature

机译：脑颅皮肤脂肪瘤病：脊髓栓系综合征的罕见关联与文献综述。
- 作者：Amal Naous;Abdel Rahman Shatila;Zeina Naja;Ahmad Salaheddine Naja;Mariam Rajab
- 期刊名称：《Child Neurology Open》 | 2015年第1期
- encephalocraniocutaneous lipomatosistethered spinal cord syndromehydrocephalus;
43.Transient Cerebral Arteriopathy in a Child Associated With Cytomegalovirus Infection:

机译：与巨细胞病毒感染相关的儿童的短暂性脑动脉病：
- 作者：Wei-Tsun Kao;Wei-Chen Lin;Yong-Hao Tseng;Tai-Heng Chen
- 期刊名称：《Child Neurology Open》 | 2015年第3期
- strokechildhoodcytomegalovirusarteriopathyinfection;
44.Ictal 99mTc-Ethyl Cysteinate Dimer SPECT Findings of a Girl With Refractory Localization-Related Epilepsy Who Developed Transient Ictal Bradycardia:

机译：Ictal 99mTc-半胱氨酸乙酯二聚体的SPECT结果，发现患有短暂性Ictal心动过缓的顽固性定位相关性癫痫的女孩：
- 作者：Tomokazu Kimizu;Hiromitsu Toshikawa;Sadami Kimura;Tae Ikeda;Yukiko Mogami;Keiko Yanagihara;Haruhiko Kishima;Yasuhiro Suzuki
- 期刊名称：《Child Neurology Open》 | 2015年第3期
- ictal bradycardiasudden unexplained death in epilepsycluster seizuresictal SPECTinsular cortex;
45.Arthrogryposis Multiplex Congenita Related to Third-Trimester Basal Ganglia Ischemia: A Case Report

机译：与晚期妊娠基底节缺血相关的关节软骨多发性先天性：一例报告
- 作者：Perrine Venot;Philippe Vo Van;Gratiella Mac Caby;Gauthier Loron;Jean Paul Bory;Ahmad Akhavi;Nathalie Bednarek
- 期刊名称：《Child Neurology Open》 | 2015年第1期
- arthrogryposishypoxica??ischemic lesionsmagnetic resonance imagingfetus;
46.Delayed Effects of Transcutaneous Organophosphate Poisoning in Four Children:

机译：四个孩子经皮有机磷中毒的延迟效应：
- 作者：Milen Pavlovic;David Neubauer;Asma A. Al-Tawari
- 期刊名称：《Child Neurology Open》 | 2015年第4期
- organophosphatesdelayedneuropathy;
47.First Application of Ketogenic Diet on a Child With Intractable Epilepsy in Ghana:

机译：生酮饮食在加纳顽固性癫痫患儿中的首次应用：
- 作者：Dezhi Cao;Eben Badoe;Yanwei Zhu;Xia Zhao;Yan Hu;Jianxiang Liao
- 期刊名称：《Child Neurology Open》 | 2015年第3期
- ketogenic dietintractable epilepsyWest AfricaGhanatreatment;
48.FOXG1 Mutation is a Low-Incidence Genetic Cause in Atypical Rett Syndrome:

机译：FOXG1突变是非典型Rett综合征的低发病遗传原因：
- 作者：Christine K. Byun;Jin Sook Lee;Byung Chan Lim;Ki Joong Kim;Yong Seung Hwang;Jong-Hee Chae
- 期刊名称：《Child Neurology Open》 | 2015年第1期
- Rett syndromeatypical phenotypeFOXG1;
49.Vagal Nerve Stimulation in the Treatment of Drug-Resistant Epileptic Encephalopathies in Inborn Errors of Metabolism: Report of 2 Cases

机译：迷走神经刺激治疗先天性代谢错误的耐药性癫痫性脑病：2例报告
- 作者：Daniele Grioni;Andrea Landi;Serena Gasperini;Andrea Trezza;Leonardo Fiori;Miriam Rigoldi;Rossella Parini;Erik Pietro Sganzerla
- 期刊名称：《Child Neurology Open》 | 2015年第4期
- drug-resistant epilepsyvagal nerve stimulationinborn errors of metabolism;
50.Prevalence and Characteristics of Chinese Patients With Duchenne and Becker Muscular Dystrophy: A Territory Wide Collaborative Study in Hong Kong

机译：中国杜兴氏和贝克氏肌营养不良患者的患病率和特征：香港地区的一项合作研究
- 作者：Sophelia H. S. Chan;Ivan F. M. Lo;Sharon W. W. Cherk;Wai Wai Cheng;Eva L. W. Fung;Wai Lan Yeung;Mary Ngan;Wing Cheong Lee;Ling Kwong;Suet Na Wong;Che Kwan Ma;Shuk Mui Tai;Grace S. F. Ng;Shun Ping Wu;Virginia C. N. Wong
- 期刊名称：《Child Neurology Open》 | 2015年第2期
- Duchenne muscular dystrophydystrophinopathyprevalenceBecker muscular dystrophyneuromuscular disorderDuchenne muscular dystrophy gene mutation;
51.Neural Correlates of Reward Processing in Typical and Atypical Development:

机译：典型和非典型发展中的奖励处理的神经相关性：
- 作者：Emma G. Duerden;Minha Lee;Stephanie Chow;Julie Sato;Kathleen Mak-Fan;Margot J. Taylor
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- rewardautism spectrum disorderpreterm birthbrain developmentfunctional MRI;
52.A Video Report of Braina??Lunga??Thyroid Syndrome in a Japanese Female With a Novel Frameshift Mutation of the NKX2-1 Gene:

机译：带有NKX2-1基因的新型移码突变的日本女性的脑-肺-甲状腺综合征的视频报道：
- 作者：Takenori Tozawa;Kenji Yokochi;Satoshi Kono;Takashi Konishi;Toshiyuki Yamamoto;Akira Nishimura;Tomohiro Chiyonobu;Masafumi Morimoto;Hajime Hosoi
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- braina??lunga??thyroid syndromeNKX2-1ataxic cerebral palsy;
53.Acute Postviral Encephalopathy: Pathologic and Radiologic Correlation in an Atypical Case

机译：急性病毒后脑病：非典型病例的病理和放射学相关性
- 作者：Adina Achiriloaie;David Michelson;Li Lei;Laura Denham;Kerby Oberg;Ravi Raghavan
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- acute necrotizing encephalopathyinfluenza-associated encephalopathypostviral;
54.Encephalopathy and Axonal Neuropathy Associated With Mycoplasma Pneumoniae Infection: Response to Intravenous Immunoglobulin Therapy

机译：与肺炎支原体感染相关的脑病和轴索性神经病：对静脉免疫球蛋白治疗的反应。
- 作者：Ali Saker;Stephanie Athman;Mohammed Aldosari;Husn Frayha
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- mycoplasmaencephalitisaxonal neuropathyintravenous immunoglobulin;
55.Stiff-Person Syndrome and Gravesa?? Disease: A Pediatric Case Report

机译：僵人综合症和格雷夫斯？疾病：儿科病例报告
- 作者：Lais Moreira Medeiros;Thulio Carvalho Morais;Arlete Esteves Lopes Primo;Valeria Casella Speltri;Maria Sheila Guimaraes Rocha
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- stiff-person syndromeanti-GADgravesa?? diseaseautoimmunespasticity;
56.An Unusual Triad in Pediatric Neurology: A Case Report on Cerebral Palsy, Epilepsy, and Duchenne Muscular Dystrophy

机译：小儿神经病学中不寻常的三联征：脑瘫，癫痫和杜兴肌营养不良症的一例报告。
- 作者：Ruben G. F. Hendriksen;Marlien W. Aalbers;Jos G. M. Hendriksen;Christine E. M. de Die-Smulders;Govert Hoogland;Johan S. H. Vles
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- cerebral palsyDuchenne muscular dystrophyepilepsydiagnostic overshadowingdystrophin;
57.Brain Inflammation in an Infant With Hemimegalencephaly, Escalating Seizures, and Epileptic Encephalopathy:

机译：患有半巨脑，癫痫发作和癫痫性脑病的婴儿的脑部炎症：
- 作者：Se Hee Kim;John J. Millichap;Sookyong Koh
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- early-onset seizuresepilepsymalformations of cortical developmenthemispherectomyneuroinflammation;
58.Pediatric Hereditary Neuralgic Amyotrophy: Successful Treatment With Intravenous Immunoglobulin and Insights Into SEPT9 Pathogenesis

机译：小儿遗传性神经性肌萎缩症：静脉注射免疫球蛋白的成功治疗及对SEPT9发病机制的认识
- 作者：Raymond Chuk;Megan Sheppard;Geoff Wallace;David Coman
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- hereditary neuralgic amyotrophyintravenous immunoglobulinSEPT9;
59.MECP2 Duplications in Symptomatic Females: Report on 3 Patients Showing the Broad Phenotypic Spectrum

机译：有症状女性的MECP2重复：3例表现出广泛表型谱的报告
- 作者：Victoria San Antonio-Arce;Mar?-a Fenollar-Cort??s;Raluca Oancea Ionescu;Teresa DeSantos-Moreno;Jes?os Gallego-Merlo;Francisco Jos?? Illana C??mara;Mar?-a Carmen Cotarelo P??rez
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- femaleMECP2 duplication syndromephenotypeXq28 microduplication including MECP2;
60.Occipital Bony Abnormality and Multiple Strokes in a Pediatric Patient: Case Report and Review of the Current Literature

机译：儿科患者的枕骨异常和多发性中风：病例报告和当前文献复习
- 作者：Thomas J. Blount;Paul D. Larsen;William E. Thorell
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- vertebral artery dissectiondistal embolizationoccipital bony growth;
61.Clinical Profile of Pediatric Neurological Disorders: Outpatient Department, Khartoum, Sudan

机译：小儿神经系统疾病的临床概况：苏丹喀土穆门诊
- 作者：Inaam Noureldyme Mohamed;Maha Abdelmoneum Elseed;Ahlam Abdalrhman Hamed
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- neurologicaldisorderschildren;
62.Further Validation of the SIGMAR1 c.151+1GT Mutation as Cause of Distal Hereditary Motor Neuropathy:

机译：SIGMAR1 c.151 + 1G> T突变作为远距离遗传性运动神经病的原因的进一步验证：
- 作者：Jessica J. Y. Lee;Clara D. M. van Karnebeek;Britt Dr??gemoller;Casper Shyr;Maja Tarailo-Graovac;Patrice Eydoux;Colin J. Ross;Wyeth W. Wasserman;Bruce Bj??rnson;John K. Wu
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- SIGMAR1sigma-1 receptordistal hereditary motor neuropathydHMNwhole exome sequencing;
63.Assessment of Subclinical Pancreatitis in Epileptic Children With Different Treatment Modalities:

机译：不同治疗方式的癫痫儿童的亚临床胰腺炎评估：
- 作者：Doa Mohamed Mahrous;Gehan Lotfy Abdel Hakeem;Reem Abdel Salam Abdel Aziz;Aliaa Monir Higazi
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- subclinical pancreatitisepilepsyantiepileptic regimens;
64.Epstein-Barr Virus-Associated Hemophagocytic Lymphohistiocytosis and Guillain-Barre Syndrome in a 16-Month-Old Child:

机译：在16个月大的儿童中，爱泼斯坦-巴尔病毒相关的噬血细胞淋巴组织细胞增生和格林-巴利综合症：
- 作者：Motohiro Matsui;Mariko Shimizu;Aya Ioi;Azusa Mayumi;Kohei Higuchi;Akihisa Sawada;Maho Sato;Masahiro Yasui;Keiko Yanagihara;Masami Inoue
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- Guillain-Barre syndromeEpstein-Barr virushemophagocytic lymphohistiocytosisintravenous immunoglobulin Gacute motor axonal neuropathy;
65.Complex Phenotype of a Boy With De Novo 16p13.3-13.2 Interstitial Deletion:

机译：De Novo 16p13.3-13.2男孩间质删除的复杂表型：
- 作者：Roberta Milone;Anna Rita Ferrari;Rosa Pasquariello;Stefania Bargagna
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- verbal dyspraxiacontinuous spike-waves during sleepnodular heterotopiamicrodeletion16p13.3-13.2;
66.De Novo 3q22.3q24 Microdeletion in a Patient With Blepharophimosisa??Ptosisa??Epicanthus Inversus Syndrome, Dandy-Walker Malformation, and Wisconsin Syndrome:

机译：De Novo 3q22.3q24微缺失在患有支原体病，Ptosisa，Epicanthus逆综合征，Dandy-Walker畸形和威斯康星综合症的患者中：
- 作者：Anand Ramineni;David Coman
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- Dy-Walker malformationmicrodeletionWisconsin syndrome;
67.A Mutation in the Tubulin-Encoding TUBB3 Gene Causes Complex Cortical Malformations and Unilateral Hypohidrosis:

机译：微管蛋白编码TUBB3基因中的突变导致复杂的皮质畸形和单侧多汗症：
- 作者：Shinobu Fukumura;Mitsuhiro Kato;Kentaro Kawamura;Akiko Tsuzuki;Hiroyuki Tsutsumi
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- TUBB3brain abnormalityunilateral hypohidrosis;
68.Pelvic-Spinal Analysis and the Impact of Onabotulinum toxin A Injections on Spinal Balance in one Child With Cerebral Palsy:

机译：一名儿童脑瘫患儿的骨盆-脊柱分析和注射肉毒杆菌毒素A对脊柱平衡的影响：
- 作者：Emmanuelle Chal??at-Valayer;Jean-Claude Bernard;Julie Deceuninck;Pierre Roussouly
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- cerebral palsybotulinum toxinchildrenassessmentpelvic-spinal balance;
69.Seizures Related to Hypomagnesemia: A Case Series and Review of the Literature

机译：与低镁血症有关的癫痫发作：一个病例系列和文献综述
- 作者：Becky Biqi Chen;Chitra Prasad;Marta Kobrzynski;Craig Campbell;Guido Filler
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- seizureshypomagnesemia with secondary hypocalcemiaTRPM6isolated recessive hypomagnesemiaGalloway-Mowat syndrome;
70.Chromosome 12p Deletion Spanning the GRIN2B Gene Presenting With a Neurodevelopmental Phenotype: A Case Report and Review of Literature

机译：跨GRIN2B基因的神经发育表型的染色体12p缺失：病例报告和文献综述。
- 作者：Navin Mishra;Elizabeth Kouzmitcheva;Angela Orsino;Berge A. Minassian
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- chromosome12p deletionCDKN1BGRIN2BETV6neurodevelopmentautism spectrum disorder;
71.Vein of Galen Aneurysmal Malformation in Neonates Presenting With Congestive Heart Failure:

机译：患有充血性心力衰竭的新生儿的盖伦动脉瘤畸形的静脉：
- 作者：Andjenie Madhuban;Freek van den Heuvel;Margriet van Stuijvenberg
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- neonatevein of Galen malformationcardiac failure;
72.A De Novo Mutation in MTND6 Causes Generalized Dystonia in 2 Unrelated Children:

机译：MTND6的从头突变导致2名无关儿童的广泛性肌张力障碍：
- 作者：Yasemin Gulcan Kurt;Jorida ??oku;H. Orhan Akman;Ali Naini;Jesheng Lu;Kristin Engelstad;Michio Hirano;Darryl C. De Vivo;Salvatore DiMauro
- 期刊名称：《Child Neurology Open》 | 2016年第2期
- dystoniaearly onsetrelatively normal livesmitochondrial DNAND6 gene;
73.Seven-Digit Creatine Kinase in Acute Rhabdomyolysis in a Child:

机译：一名儿童急性横纹肌溶解症的七位肌酸激酶：
- 作者：Nuha Basheer;Sirin Mneimneh;Mariam Rajab
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- rhabdomyolysischild;
74.Novel LRPPRC Mutation in a Boy With Mild Leigh Syndrome, Frencha??Canadian Type Outside of Qu??bec:

机译：在患有轻度李氏综合征的男孩中的新型LRPPRC突变，来自Qu ?? bec以外的Frencha ?? Canadian型：
- 作者：Velda Xinying Han;Teresa S. Tan;Furene S. Wang;Stacey Kiat-Hong Tay
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- childrendevelopmental delayepilepsymetabolismmitochondrial disorderneurodevelopment;
75.Distal 22q11.2 Microduplication: Case Report and Review of the Literature

机译：远端22q11.2微复制：病例报告和文献复习
- 作者：Elana Pinchefsky;Laurence Laneuville;Myriam Srour
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- developmental delaygeneticsintellectual disabilityneurodevelopmentpediatric;
76.Rapid Resolution of Enterovirus 71-Associated Opsoclonus Myoclonus Syndrome on Intravenous Immunoglobulin:

机译：快速解决肠道病毒71相关的Ossoclonus Myoclonus综合征对静脉免疫球蛋白的作用：
- 作者：Ahmed Sahly;Laurence Gauquelin;Guillaume S??bire
- 期刊名称：《Child Neurology Open》 | 2017年第2期
- CerebellitisNeuroinflammationParaneoplasic SyndromeGlucocorticoids;
77.Biotin-Thiamine-Responsive Basal Ganglia Disease: Case Report and Follow-Up of a Patient With Poor Compliance

机译：生物素 - 硫胺素响应基底神经节病：案例报告和遵守差患者的后续行动
- 作者：Muneera A. Alabdulqader;Sumayah Al Hajjaj
- 期刊名称：《Child Neurology Open》 | 2018年第3期
- biotin-thiamine-responsive basal ganglia diseasebiotin-responsive basal ganglia diseasethiaminebiotin;
78.Afebrile Benign Convulsion Associated With Mild Gastroenteritis

机译：与轻度胃肠炎相关的消肿良性惊厥
- 作者：Nahid Khosroshahi;Aliakbar Rahbarimanesh;Farhad Asadi Boroujeni;Zahra Eskandarizadeh;Mojdeh Habibi Zoham
- 期刊名称：《Child Neurology Open》 | 2018年第3期
- benignconvulsive seizuresgastroenteritisinfant;
79.Ketogenic Diet in Refractory Childhood Epilepsy

机译：在难治性儿童癫痫中的酮味饮食
- 作者：Amerins Weijenberg;Margreet van Rijn;Petra M. C. Callenbach;Tom J. de Koning;Oebele F. Brouwer
- 期刊名称：《Child Neurology Open》 | 2018年第3期
- ketogenic dietchildhoodrefractory epilepsyliquid diet introductionoutpatient setting;
80.Vibration-Assisted Home Training Program for Children With Spinal Muscular Atrophy

机译：脊髓肌肉萎缩儿童的振动辅助家庭培训计划
- 作者：Christina Stark;Ibrahim Duran;Sebahattin Cirak;Stefanie Hamacher;Heike-Katharina Hoyer-Kuhn;Oliver Semler;Eckhard Schoenau
- 期刊名称：《Child Neurology Open》 | 2018年第3期
- childrendevelopmental disabilityefficacypediatricrehabiliation;
81.A Gut Feeling

机译：一个肠道的感觉
- 作者：Xue Ming;Neil Chen;Carly Ray;Gretchen Brewer;Jeffrey Kornitzer;Robert A. Steer
- 期刊名称：《Child Neurology Open》 | 2018年第3期
- attention-deficit/hyperactivity disorder (ADHD)microbiomegastrointestinal (GI) disordersimmune dysregulation;
82.Novel PLP1 Mutations Identified With Next-Generation Sequencing Expand the Spectrum of PLP1-Associated Leukodystrophy Clinical Phenotypes

机译：用下一代测序鉴定的新型PLP1突变扩大了PLP1相关的白科医疗临床表型的谱
- 作者：Rebecca L. Margraf;Jacob Durtschi;Bryan Krock;Tara M. Newcomb;Joshua L. Bonkowsky;Karl V. Voelkerding;Pinar Bayrak-Toydemir;Richard E. Lutz;Kathryn J. Swoboda
- 期刊名称：《Child Neurology Open》 | 2018年第3期
- Pelizaeus-Merzbacher diseaseproteolipid protein 1spastic paraplegia type 2PLP1leukodystrophyPMDSPG2dystoniabraindevelopmental delaygeneticsmutationnext-generation sequencingspasticity;
83.Worster-Drought Syndrome Associated With LINS Mutations

机译：与液体突变相关的流动干旱综合征
- 作者：Hugh J. McMillan;Anne-Lise Holahan;Julie Richer
- 期刊名称：《Child Neurology Open》 | 2018年第3期
- Worster-Drought syndromeaphoniadevelopmental disabilitiesLINSpseudobulbar paresis;
84.A Case of Delayed-Onset Posthypoxic Leukoencephalopathy in a Pediatric Patient

机译：儿科患者中延迟发作的延迟性毒性白血病病例
- 作者：Kristen Smolinsky;Ivona Sediva
- 期刊名称：《Child Neurology Open》 | 2018年第3期
- Posthypoxic Leukoencephalopathysevere hypoxic brain injuryaltered mental status, pediatric?;
85.A Retrospective Analysis of the Long-Term Outcome of Drug-Resistant Epilepsy in Children Treated in Urban India

机译：对印度儿童耐药性癫痫的长期结果的回顾性分析
- 作者：Toranj Raimalwalla;Vrajesh Udani;Dimpi Mhatre
- 期刊名称：《Child Neurology Open》 | 2018年第3期
- antiepileptic drugschildrenepilepsyoutcomepediatricdrug-resistantrisk factors;
86.Intensive Combination Immunotherapy and Neuroinflammation Resolution in a Child With Anti-PCA-1 (Yo) Paraneoplastic Syndrome and 2 Malignancies

机译：抗PCA-1（yo）平原综合征和2个恶性肿瘤儿童中的强化组合免疫疗法和神经炎性分辨率
- 作者：Guillermo Philipps;Elizabeth D. Tate;Michael R. Pranzatelli
- 期刊名称：《Child Neurology Open》 | 2018年第3期
- PCA-1 syndromepediatric neuroinflammatory disordersadrenocortical carcinomaDown syndromeOMSpediatric paraneoplastic cerebellar degenerationacute lymphoblastic leukemiacytosine arabinoside-induced ataxiaANNA-1 (Hu) syndrome;
87.A Case With 4 de Novo Copy Number Variations With Clinical Features That Overlap 1q43q44 Microdeletion and 3q29 Microduplication Syndromes

机译：具有4 de Novo拷贝数变异的案例，具有重叠1Q4344微缺失和3Q29微量综合综合征的临床特征
- 作者：Miriam Kessi;Jing Peng;Lifen Yang;Haolin Duan;Yulin Tang;Fei Yin
- 期刊名称：《Child Neurology Open》 | 2018年第3期
- 1q43q44 microdeletion syndrome3q29 microduplication syndromeHNRNPUcorpus callosum dysplasiamicrocephaly;
88.Impact of Transcranial Direct Current Stimulation on Reading Skills of Children and Adolescents With Dyslexia

机译：经颅直流刺激对综合带综合症患儿童和青少年阅读技巧的影响
- 作者：Débora Medeiros Rios;Mino Correia Rios;Igor Dórea Bandeira;Fernanda Queiros Campbell;Daniel de Carvalho Vaz;Rita Lucena
- 期刊名称：《Child Neurology Open》 | 2018年第3期
- dyslexianeuromodulationnoninvasive brain stimulationtranscranial direct current stimulationchildren;
89.Autism Spectrum Disorder and Neonatal Serum Magnesium Levels in Preterm Infants

机译：早产儿的自闭症谱系障碍和新生儿血清镁水平
- 作者：Amanda V. Bakian;Deborah A. Bilder;E. Kent Korgenski;Joshua L. Bonkowsky
- 期刊名称：《Child Neurology Open》 | 2018年第3期
- autismmagnesiumprematuritypreterm;
90.Functional Gains in Children With Spastic Hemiplegia Following a Tendon Achilles Lengthening Using Computerized Adaptive Testing—A Pilot Study

机译：使用计算机适应性测试 - 试验研究施用肌腱角质膨胀后痉挛性偏瘫的儿童功能性增益
- 作者：Eli Saleh;Noémi Dahan-Oliel;Kathleen Montpetit;Thierry Benaroch;Rita Yap;Nadia Barakat;M. J. Mulcahey
- 期刊名称：《Child Neurology Open》 | 2018年第3期
- spastic hemiplegiacomputer adaptive testingfunctional outcomestendon Achilles lengthening;
91.Autoimmune Ataxia During Maintenance Therapy for Acute Lymphoblastic Leukemia

机译：急性淋巴细胞白血病维持治疗期间的自身免疫共济失调
- 作者：Julie Voeller;Chrysanthy Ikonomidou;Justin Brucker;Carol Diamond;Sharon Frierdich;Neha Patel
- 期刊名称：《Child Neurology Open》 | 2018年第3期
- autoimmune ataxiaautoimmune encephalitisacute lymphoblastic leukemiapediatricmaintenance chemotherapy;
92.Acute Encephalopathy With Biphasic Seizures and Late Reduced Diffusion Associated With Adenoviral Pneumonia

机译：具有双相癫痫发作的急性脑病，并且与腺病毒肺炎相关的延迟减少
- 作者：Keun Soo Lee;Bo Lyun Lee;Young Jin Heo
- 期刊名称：《Child Neurology Open》 | 2019年第3期
- acute febrile encephalopathyadenovirusseizures;
93.A Rare Case of Bartonella Encephalitis With Hemiplegia

机译：一种罕见的Bartonella脑炎与偏瘫
- 作者：Laura Rosas;Kavya Rao;Christine McGough;Ashley Becker
- 期刊名称：《Child Neurology Open》 | 2019年第3期
- EEGelectroencephalogrampediatricadolescentsencephalitisTodd paralysisinfectious diseasecat scratch diseaseepidemiology;
94.A Not So Benign Family Pedigree With Hereditary Chorea: A Broader Phenotypic Expression or Additional Picture?

机译：一个没有那么良性的家族血统与遗传性舞会：更广泛的表型表达或其他图片？
- 作者：Roberta Milone;Riccardo Masson;Caterina Di Cosmo;Massimo Tonacchera;Veronica Bertini;Andrea Guzzetta;Roberta Battini
- 期刊名称：《Child Neurology Open》 | 2019年第3期
- motor delayhypotoniaataxiaintellectual disabilityautism spectrum disorder;
95.AIMP1 Mutation Long-Term Follow-Up, With Decreased Brain N-Acetylaspartic Acid and Secondary Mitochondrial Abnormalities

机译：AIMP1突变长期随访，脑N-乙酰天冬氨酸和次级线粒体异常降低
- 作者：Aneal Khan;Jennifer Bennett;Morris H. Scantlebury;Xing-Chang Wei;Marina Kerr
- 期刊名称：《Child Neurology Open》 | 2019年第3期
- AIMP1Nmitochondrial abnormalitiesseizures;
96.Development, Implementation, and Use of a Neurology Therapeutics Committee

机译：神经内科治疗委员会的开发，实施和使用
- 作者：Edward B. Clark;Russell J. Butterfield;Francis M. Filloux;Joshua L. Bonkowsky
- 期刊名称：《Child Neurology Open》 | 2019年第3期
- therapeuticspediatric neurologynusinersengene therapyspinal muscular atrophy;
97.MRI-Negative Myelitis Associated With Myelin Oligodendrocyte Glycoprotein Antibody Spectrum Demyelinating Disease

机译：MRI阴性骨髓炎与髓鞘寡核细胞糖蛋白抗体谱脱髓鞘疾病相关
- 作者：Carlos A. Pérez;Stephanie Garcia-Tarodo;Regina Troxell
- 期刊名称：《Child Neurology Open》 | 2019年第3期
- myelin oligodendrocyte glycoprotein antibodychildrenseizuresrelapsingmyelitisacute demyelinating syndrome;
98.CLIPPERS Spectrum Disorder: A Rare Pediatric Neuroinflammatory Condition

机译：快船谱紊乱：罕见的小儿神经炎症病症
- 作者：Tarishi Nemani;Anaita Udwadia-Hegde;Purva Keni Karnavat;Ritu Kashikar;Shridhar Epari
- 期刊名称：《Child Neurology Open》 | 2019年第3期
- Pediatric CLIPPERSNeuro-inflammatoryAtaxiaMethotrexate;
99.Glycine Transporter 1 Encephalopathy From Biochemical Pathway to Clinical Disease: Review

机译：甘氨酸转运蛋白1从生化途径到临床疾病的脑病：审查
- 作者：Rayan Alfallaj;Majid Alfadhel
- 期刊名称：《Child Neurology Open》 | 2019年第3期
- GLYT1 encephalopathyGLYT1 transporter dysfunctionSLC6A9autosomal recessive nonketotic hyperglycinemia;
100.Long-Term Exposure and Safety of a Novel Topical Rapamycin Cream for the Treatment of Facial Angiofibromas in Tuberous Sclerosis Complex: Results From a Single-Center, Open-Label Trial

机译：一种新型局部雷帕霉素乳膏的长期暴露和安全性，用于治疗肿块硬化复合体中的面部血管纤维蛋白酶：单中心，开放标签试验结果
- 作者：Margaret C. Wheless;Apana A. Takwi;Hassan Almoazen;James W. Wheless
- 期刊名称：《Child Neurology Open》 | 2019年第3期
- tuberous sclerosis complexangiofibromarapamycintreatment;

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