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Child Neurology Open

【机译】：儿童神经病开放

ISSN：-
出版周期：Quarterly, 2015
语言：English

起始发布年份：2014
出版者：[Thousand Oaks, Calif.] : SAGE Publications Inc., [2014]-
出版地：United States

数据库引入：PubMed: v1n1, Jul.-Sept. 2014-, PMC

MeSH词表主题词：Nervous System Diseases*; Pediatrics*

备注：Numbering from contents page. Volume 1 complete in one issue. Description based展开▼

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1.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
2.Anterior Commissure Involvement in Humanherpes Virus 6 Encephalitis

机译：人疱疹病毒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 fiber human herpesvirus 6 magnetic resonance imaging cytotoxic edema;
3.Connexin 43 and Its Hemichannels Mediate Hypoxia–Ischemia-Induced Cell Death in Neonatal Rats

机译：连接蛋白43及其半通道介导缺氧缺血诱导的新生大鼠细胞死亡。
- 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 43 gap junction hemichannel astrocytes hypoxia–ischemia (HI) oxygen–glucose deprivation (OGD) neuroprotection;
4.A Case Report of Homocystinuria With Dystonia and Stroke

机译：同型尿毒症合并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
- homocysteine movement disorder cerebrovascular disease;
5.Neuro-Behçets in a Child

机译：一个孩子的神经行为
- 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
- MRI uveitis vitritis papillitis hypertonia incontinence urinary tract infection azathioprine;
6.Childhood-Onset Progressive Dystonia With Mitochondrial DNA G14459A Mutation

机译：线粒体DNA G14459A突变的儿童期进展性肌张力障碍
- 作者：Ayaka Koide;Hiroshi Ozawa;Masaya Kubota;Yuichi Goto
- 期刊名称：《Child Neurology Open》 | 2014年第1期
- mitochondrial DNA Leber hereditary optic neuropathy dystonia;
7.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研究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病的女孩
- 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 bradycardia sudden unexplained death in epilepsy cluster seizures ictal SPECT insular cortex;
8.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
- stroke childhood cytomegalovirus arteriopathy infection;
9.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 diet intractable epilepsy West Africa Ghana treatment;
10.A New Observation of an Atypical and Severe Variant of the Guillain-Barre Syndrome in a Child

机译：儿童格林-巴利综合症的非典型和严重变异的新观察
- 作者：Linda Pons;Véronique Manel;Dorothée Ville;Etienne Javouhey;Fabienne Bordet
- 期刊名称：《Child Neurology Open》 | 2015年第4期
- Guillain-Barré syndrome pediatrics Mycoplasma pneumonia;
11.Guillain Barré Syndrome in a Child With X-Linked Adrenoleukodystrophy

机译：X联肾上腺皮质营养不良症患儿的格林格林Barré综合征
- 作者：Ron Jacob;Hanna Mandel;Naim Shehadeh
- 期刊名称：《Child Neurology Open》 | 2015年第4期
- pediatric neurology autoimmune Addison’s disease;
12.Vagal Nerve Stimulation in the Treatment of Drug-Resistant Epileptic Encephalopathies in Inborn Errors of Metabolism

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。
- 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 epilepsy vagal nerve stimulation inborn errors of metabolism;
13.Assessing Children With Disabilities Using WHO International Classification of Functioning Disability and Health Child and Youth Version Activities and Participation D Codes

机译：使用世界卫生组织功能残疾与健康国际分类的残疾儿童评估少年和青少年版本活动和参与D代码
- 作者：Niels Ove Illum;Kim Oren Gradel
- 期刊名称：《Child Neurology Open》 | 2015年第4期
- childhood disability International Classification of Functioning Disability and Health child and youth version d codes psychometrics Rasch data analysis;
14.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有关吗？
- 作者：Yingjun Xie
- 期刊名称：《Child Neurology Open》 | 2015年第4期
- autism 15q13.3 microduplication CMA-SNP array CHRNA7 oral clefts;
15.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
- organophosphates delayed neuropathy;
16.Clinical Phenotype of De Novo GNAO1 Mutation

机译：De Novo GNAO1突变的临床表型
- 作者：Inga Talvik;Rikke S. Møller;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 encephalopathy ohtahara syndrome GNAO1 mutation next generation sequencing gene panel;
17.Prevalence and Characteristics of Chinese Patients With Duchenne and Becker Muscular Dystrophy

机译：中国杜兴氏和贝克肌营养不良患者的患病率和特征
- 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 dystrophy dystrophinopathy prevalence Becker muscular dystrophy neuromuscular disorder Duchenne muscular dystrophy gene mutation;
18.Epstein-Barr Virus-Associated Hemophagocytic Lymphohistiocytosis and Guillain-Barre Syndrome in a 16-Month-Old Child

机译：爱泼斯坦-巴尔病毒相关的血吞噬性淋巴细胞组织细胞增生症和格林-巴利综合征在一个16个月大的儿童中。
- 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-1期
- Guillain-Barre syndrome Epstein-Barr virus hemophagocytic lymphohistiocytosis intravenous immunoglobulin G acute motor axonal neuropathy;
19.A De Novo Mutation in MTND6 Causes Generalized Dystonia in 2 Unrelated Children

机译：从头突变的MTND6导致2名无关儿童的广泛性肌张力障碍。
- 作者：Yasemin Gulcan Kurt;Jorida Çoku;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-1期
- dystonia early onset relatively normal lives mitochondrial DNA ND6 gene;
20.Chromosome 12p Deletion Spanning the GRIN2B Gene Presenting With a Neurodevelopmental Phenotype

机译：跨过GRIN2B基因的12p染色体缺失与神经发育表型的关系
- 作者：Navin Mishra;Elizabeth Kouzmitcheva;Angela Orsino;Berge A. Minassian
- 期刊名称：《Child Neurology Open》 | 2016年第-1期
- chromosome12p deletion CDKN1B GRIN2B ETV6 neurodevelopment autism spectrum disorder;
21.Brain Inflammation in an Infant With Hemimegalencephaly Escalating Seizures and Epileptic Encephalopathy

机译：患有半巨脑症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-1期
- early-onset seizures epilepsy malformations of cortical development hemispherectomy neuroinflammation;
22.An Unusual Triad in Pediatric Neurology

机译：小儿神经内科异常
- 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-1期
- cerebral palsy Duchenne muscular dystrophy epilepsy diagnostic overshadowing dystrophin;
23.A Video Report of Brain–Lung–Thyroid Syndrome in a Japanese Female With a Novel Frameshift Mutation of the NKX2-1 Gene

机译：带有NKX2-1基因新型移码突变的日本女性脑-肺-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-1期
- brain–lung–thyroid syndrome NKX2-1 ataxic cerebral palsy;
24.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-1期
- TUBB3 brain abnormality unilateral hypohidrosis;
25.De Novo 3q22.3q24 Microdeletion in a Patient With Blepharophimosis–Ptosis–Epicanthus Inversus Syndrome Dandy-Walker Malformation and Wisconsin Syndrome

机译：De Novo 3q22.3q24微缺失在患有支原体增生-上睑下垂-Epicanthus Inversus综合征Dandy-Walker畸形和威斯康星综合征的患者中
- 作者：Anand Ramineni;David Coman
- 期刊名称：《Child Neurology Open》 | 2016年第-1期
- Dandy-Walker malformation microdeletion Wisconsin syndrome;
26.Pediatric Hereditary Neuralgic Amyotrophy

机译：小儿遗传性神经性肌萎缩症
- 作者：Raymond Chuk;Megan Sheppard;Geoff Wallace;David Coman
- 期刊名称：《Child Neurology Open》 | 2016年第-1期
- hereditary neuralgic amyotrophy intravenous immunoglobulin SEPT9;
27.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 Drögemoller;Casper Shyr;Maja Tarailo-Graovac;Patrice Eydoux;Colin J. Ross;Wyeth W. Wasserman;Bruce Björnson;John K. Wu
- 期刊名称：《Child Neurology Open》 | 2016年第-1期
- SIGMAR1 sigma-1 receptor distal hereditary motor neuropathy dHMN whole exome sequencing;
28.Complex Phenotype of a Boy With De Novo 16p13.3-13.2 Interstitial Deletion

机译：De Novo男孩的复杂表型16p13.3-13.2间隙删除
- 作者：Roberta Milone;Anna Rita Ferrari;Rosa Pasquariello;Stefania Bargagna
- 期刊名称：《Child Neurology Open》 | 2016年第-1期
- verbal dyspraxia continuous spike-waves during sleep nodular heterotopia microdeletion 16p13.3-13.2;
29.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 Chaléat-Valayer;Jean-Claude Bernard;Julie Deceuninck;Pierre Roussouly
- 期刊名称：《Child Neurology Open》 | 2016年第-1期
- cerebral palsy botulinum toxin children assessment pelvic-spinal balance;
30.Clinical Profile of Pediatric Neurological Disorders

机译：小儿神经系统疾病的临床概况
- 作者：Inaam Noureldyme Mohamed;Maha Abdelmoneum Elseed;Ahlam Abdalrhman Hamed
- 期刊名称：《Child Neurology Open》 | 2016年第-1期
- neurological disorders children;
31.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-1期
- neonate vein of Galen malformation cardiac failure;
32.MECP2 Duplications in Symptomatic Females

机译：有症状女性的MECP2重复
- 作者：Victoria San Antonio-Arce;María Fenollar-Cortés;Raluca Oancea Ionescu;Teresa DeSantos-Moreno;Jesús Gallego-Merlo;Francisco José Illana Cámara;María Carmen Cotarelo Pérez
- 期刊名称：《Child Neurology Open》 | 2016年第-1期
- female MECP2 duplication syndrome phenotype Xq28 microduplication including MECP2;
33.Assessment of Subclinical Pancreatitis in Epileptic Children With Different Treatment Modalities

机译：癫痫儿童不同治疗方式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-1期
- subclinical pancreatitis epilepsy antiepileptic regimens;
34.Acute Postviral Encephalopathy

机译：急性病毒后脑病
- 作者：Adina Achiriloaie;David Michelson;Li Lei;Laura Denham;Kerby Oberg;Ravi Raghavan
- 期刊名称：《Child Neurology Open》 | 2016年第-1期
- acute necrotizing encephalopathy influenza-associated encephalopathy postviral;
35.Neural Correlates of Reward Processing in Typical and Atypical Development

机译：典型和非典型发展中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-1期
- reward autism spectrum disorder preterm birth brain development functional MRI;
36.Seizures Related to Hypomagnesemia

机译：与低镁血症有关的癫痫发作
- 作者：Becky Biqi Chen;Chitra Prasad;Marta Kobrzynski;Craig Campbell;Guido Filler
- 期刊名称：《Child Neurology Open》 | 2016年第-1期
- seizures hypomagnesemia with secondary hypocalcemia TRPM6 isolated recessive hypomagnesemia Galloway-Mowat syndrome;
37.Encephalopathy and Axonal Neuropathy Associated With Mycoplasma Pneumoniae Infection

机译：与肺炎支原体感染相关的脑病和轴突神经病
- 作者：Ali Saker;Stephanie Athman;Mohammed Aldosari;Husn Frayha
- 期刊名称：《Child Neurology Open》 | 2016年第-1期
- mycoplasma encephalitis axonal neuropathy intravenous immunoglobulin;
38.Occipital Bony Abnormality and Multiple Strokes in a Pediatric Patient

机译：儿科患者的枕骨异常和多发性中风
- 作者：Thomas J. Blount;Paul D. Larsen;William E. Thorell
- 期刊名称：《Child Neurology Open》 | 2016年第-1期
- vertebral artery dissection distal embolization occipital bony growth;
39.Stiff-Person Syndrome and Graves’ Disease

机译：僵人综合征和格雷夫斯病
- 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-1期
- stiff-person syndrome anti-GAD graves’ disease autoimmune spasticity;
40.Use of Magnesium Sulfate Infusion for the Management of Febrile Illness-Related Epilepsy Syndrome

机译：硫酸镁输注治疗高热疾病相关性癫痫综合征
- 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 syndrome refractory status epilepticus magnesium sulfate infusion;
41.Encephalocraniocutaneous Lipomatosis

机译：脑颅皮肤脂肪瘤病
- 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 lipomatosis tethered spinal cord syndrome hydrocephalus;
42.Spontaneous Malignant Transformation of a Pilocytic Astrocytoma of Cerebellum

机译：小脑星形星形细胞瘤的自发恶性转化
- 作者：Joana Coelho;Sofia Nunes;Duarte Salgado
- 期刊名称：《Child Neurology Open》 | 2015年第1期
- low-grade gliomas pilocytic astrocytoma malignant transformation;
43.Newly Identified Characteristics and Suggestions for Diagnosis and Treatment of Diffuse Leptomeningeal Glioneuronal/Neuroepithelial Tumors

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断和治疗建议
- 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 enhancement intraparenchymal cysts leptomeningeal glioneuronal tumor neuroepithelial tumor;
44.Arthrogryposis Multiplex Congenita Related to Third-Trimester Basal Ganglia Ischemia

机译：与晚期妊娠基底节缺血相关的关节型多发性先天性
- 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
- arthrogryposis hypoxic–ischemic lesions magnetic resonance imaging fetus;
45.FOXG1 Mutation is a Low-Incidence Genetic Cause in Atypical Rett Syndrome

机译：FOXG1突变是非典型Rett综合征的低发病率遗传原因。
- 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 syndrome atypical phenotype FOXG1;
46.Acute Transverse Myelitis Caused by Echovirus 11 in a Pediatric Patient

机译：小儿患者中由Echovirus 11引起的急性横贯性脊髓炎
- 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-1期
- encephalitis epidemiology magnetic resonance imaging MRI pediatric enterovirus acute flaccid myelitis viral meningoencephalitis;
47.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突变在一例婴儿癫痫发作中转移为小儿痉挛的局灶性癫痫发作。
- 作者：Haolin Duan;Jing Peng;Miriam Kessi;Fei Yin
- 期刊名称：《Child Neurology Open》 | 2018年第-1期
- KCNQ2 gene mutation epilepsy of infancy with migrating focal seizures infantile spasms.;
48.Spinal Muscular Atrophy With Respiratory Distress Type 1—A Child With Atypical Presentation

机译：患有1型呼吸窘迫的脊髓性肌萎缩症—儿童表现不典型
- 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-1期
- SMARD1 IGHMBP2 gene congenital heart disease neuropathy children;
49.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-1期
- central pontine myelinolysis extrapontine myelinolysis methylprednisolone;
50.Novel PLP1 Mutations Identified With Next-GenerationSequencing Expand the Spectrum of PLP1-Associated Leukodystrophy ClinicalPhenotypes

机译：下一代鉴定出新型PLP1突变测序扩大了与PLP1相关的白细胞营养不良临床的范围表型
- 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-1期
- Pelizaeus-Merzbacher disease proteolipid protein 1 spastic paraplegia type 2 PLP1 leukodystrophy PMD SPG2 dystonia brain developmental delay genetics mutation next-generation sequencing spasticity;
51.Worster-Drought Syndrome Associated With LINS Mutations

机译：与LINS突变相关的渥斯特干旱综合症
- 作者：Hugh J. McMillan;Anne-Lise Holahan;Julie Richer
- 期刊名称：《Child Neurology Open》 | 2018年第-1期
- Worster-Drought syndrome aphonia developmental disabilities LINS pseudobulbar paresis;
52.Intensive Combination Immunotherapy and Neuroinflammation Resolution in aChild With Anti-PCA-1 (Yo) Paraneoplastic Syndrome and 2 Malignancies

机译：强化联合免疫治疗和神经炎症消退患有抗PCA-1（Yo）副肿瘤综合征和2例恶性肿瘤的儿童
- 作者：Guillermo Philipps;Elizabeth D. Tate;Michael R. Pranzatelli
- 期刊名称：《Child Neurology Open》 | 2018年第-1期
- PCA-1 syndrome pediatric neuroinflammatory disorders adrenocortical carcinoma Down syndrome OMS pediatric paraneoplastic cerebellar degeneration acute lymphoblastic leukemia cytosine arabinoside-induced ataxia ANNA-1 (Hu) syndrome;
53.A Case With 4 de Novo Copy Number Variations With Clinical Features ThatOverlap 1q43q44 Microdeletion and 3q29 Microduplication Syndromes

机译：一例具有4 de Novo拷贝数变异且具有临床特征的病例重叠的1q43q44微缺失和3q29微复制综合征
- 作者：Miriam Kessi;Jing Peng;Lifen Yang;Haolin Duan;Yulin Tang;Fei Yin
- 期刊名称：《Child Neurology Open》 | 2018年第-1期
- 1q43q44 microdeletion syndrome 3q29 microduplication syndrome HNRNPU gene corpus callosum dysplasia microcephaly;
54.PRUNE Syndrome Is a New Neurodevelopmental Disorder

机译：PRUNE综合征是一种新的神经发育障碍
- 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-1期
- PRUNE syndrome PRUNE1 progressive microcephaly spasticity developmental delay;
55.Atypical Rett Syndrome and Intractable Epilepsy With Novel GRIN2B Mutation

机译：非典型瑞特综合征和顽固性癫痫与新型GRIN2B突变。
- 作者：Paulina Kyriakopoulos;Vanda McNiven;Melissa T. Carter;Peter Humphreys;David Dyment;Tadeu A. Fantaneanu
- 期刊名称：《Child Neurology Open》 | 2018年第-1期
- atypical Rett syndrome epilepsy GRIN2B memantine;
56.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-1期
- fulminant ADEM acute disseminated encephalomyelitis cyclophosphamide plasmapheresis methylprednisolone;
57.Intracranial Hemorrhage and Autoimmune Thrombocytopenia in a Neonate

机译：新生儿颅内出血和自身免疫性血小板减少
- 作者：Andrea Becocci;Cristina Felice-Civitillo;Méryle Laurent;Françoise Boehlen;Roberta De Luca;Joel Fluss
- 期刊名称：《Child Neurology Open》 | 2018年第-1期
- autoimmune brain magnetic resonance imaging neonatal seizures neonate neuroimaging seizures;
58.Biotin-Thiamine-Responsive Basal Ganglia Disease: Case Report and Follow-Up of a Patient With Poor Compliance

机译：生物素-硫胺素反应性基底节疾病：病例报告和依从性差的患者的随访。
- 作者：Muneera A. Alabdulqader;Sumayah Al Hajjaj
- 期刊名称：《Child Neurology Open》 | 2018年第-1期
- biotin-thiamine-responsive basal ganglia disease biotin-responsive basal ganglia disease thiamine biotin;
59.Afebrile Benign Convulsion Associated With Mild Gastroenteritis

机译：轻度良性惊厥伴轻度胃肠炎
- 作者：Nahid Khosroshahi;Aliakbar Rahbarimanesh;Farhad Asadi Boroujeni;Zahra Eskandarizadeh;Mojdeh Habibi Zoham
- 期刊名称：《Child Neurology Open》 | 2018年第-1期
- benign convulsive seizures gastroenteritis infant;
60.Ketogenic Diet in Refractory Childhood Epilepsy

机译：生酮饮食治疗难治性儿童癫痫
- 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-1期
- ketogenic diet childhood refractory epilepsy liquid diet introduction outpatient setting;
61.Vibration-Assisted Home Training Program for Children With Spinal Muscular Atrophy

机译：脊髓型肌萎缩症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-1期
- children developmental disability efficacy pediatric rehabiliation;
62.A Case of Delayed-Onset Posthypoxic Leukoencephalopathy in a PediatricPatient

机译：小儿迟发性缺氧性脑白质病一例患者
- 作者：Kristen Smolinsky;Ivona Sediva
- 期刊名称：《Child Neurology Open》 | 2018年第-1期
- Posthypoxic Leukoencephalopathy severe hypoxic brain injury altered mental status pediatric;
63.A Retrospective Analysis of the Long-Term Outcome of Drug-Resistant Epilepsyin Children Treated in Urban India

机译：耐药性癫痫长期疗效的回顾性分析印度城市治疗儿童的比例
- 作者：Toranj Raimalwalla;Vrajesh Udani;Dimpi Mhatre
- 期刊名称：《Child Neurology Open》 | 2018年第-1期
- antiepileptic drugs children epilepsy outcome pediatric drug-resistant risk factors;
64.Impact of Transcranial Direct Current Stimulation on Reading Skills of Children and Adolescents With Dyslexia

机译：经颅直流电刺激对阅读障碍儿童的阅读能力的影响
- 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-1期
- dyslexia neuromodulation noninvasive brain stimulation transcranial direct current stimulation children;
65.Autism Spectrum Disorder and Neonatal Serum Magnesium Levels in Preterm Infants

机译：早产儿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-1期
- autism magnesium prematurity preterm;
66.Functional Gains in Children With Spastic Hemiplegia Following a Tendon Achilles Lengthening Using Computerized Adaptive Testing—A Pilot Study

机译：使用计算机自适应测试的肌腱跟腱延长后痉挛性偏瘫儿童的功能获得性研究
- 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-1期
- spastic hemiplegia computer adaptive testing functional outcomes tendon Achilles lengthening;
67.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性共济失调
- 作者：Julie Voeller;Chrysanthy Ikonomidou;Justin Brucker;Carol Diamond;Sharon Frierdich;Neha Patel
- 期刊名称：《Child Neurology Open》 | 2018年第-1期
- autoimmune ataxia autoimmune encephalitis acute lymphoblastic leukemia pediatric maintenance chemotherapy;
68.A Gut Feeling

机译：胆量的感觉
- 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-1期
- attention-deficit/hyperactivity disorder (ADHD) microbiome gastrointestinal (GI) disorders immune dysregulation;
69.2017 Reviewer Acknowledgment

机译：2017年审稿人致谢
- 期刊名称：《Child Neurology Open》 | 2018年第-1期
70.Seven-Digit Creatine Kinase in Acute Rhabdomyolysis in a Child

机译：七糖肌酸激酶在儿童急性横纹肌溶解中的作用
- 作者：Nuha Basheer;Sirin Mneimneh;Mariam Rajab
- 期刊名称：《Child Neurology Open》 | 2017年第-1期
- rhabdomyolysis child;
71.Two Novel KCNQ2 Mutations in 2 Families With Benign Familial Neonatal Convulsions

机译：在两个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-1期
- benign familial neonatal convulsions BFNC KCNQ2;
72.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Dravet综合征更广谱的存在性问题
- 作者：Maria P. Gontika;Christopher Konialis;Constantine Pangalos;Antigone Papavasiliou
- 期刊名称：《Child Neurology Open》 | 2017年第-1期
- epileptic encephalopathy infant genetics mutation next generation sequencing;
73.Temporary Efficacy of Pyrimethamine in Juvenile-Onset Tay-Sachs Disease Caused by 2 Unreported HEXA Mutations in the Indian Population

机译：乙胺嘧啶在印度人口中由2个未报告的HEXA突变引起的青少年性Tay-Sachs病的临时疗效
- 作者：Anaita Udwadia-Hegde;Omkar Hajirnis
- 期刊名称：《Child Neurology Open》 | 2017年第-1期
- juvenile Tay-Sachs disease hexosaminidase A compound heterozygous pyrimethamine India;
74.Visceral Hyperalgesia

机译：内脏痛觉过敏
- 作者：Joseph Asaro;Christine A. Robinson;Philip T. Levy
- 期刊名称：《Child Neurology Open》 | 2017年第-1期
- gabapentin visceral hyperalgesia neonates neuropathic pain;
75.Hyperostosis Frontalis Interna in a Child With Severe Traumatic Brain Injury

机译：严重创伤性脑损伤患儿的额骨额叶增生症
- 作者：Yaxiong Li;Xin Wang;Yan Li
- 期刊名称：《Child Neurology Open》 | 2017年第-1期
- hyperostosis benign bone lesions frontal bone child brain trauma;
76.A Case of Brown-Vialetto-Van Laere Syndrome Due To a Novel Mutation in SLC52A3 Gene

机译：SLC52A3基因新突变导致布朗-维亚莱托-范莱尔综合征的一例
- 作者：Venkatraman Thulasi;Aravindhan Veerapandiyan;Beth A. Pletcher;Chun M. Tong;Xue Ming
- 期刊名称：《Child Neurology Open》 | 2017年第-1期
- riboflavin transporter deficiency Brown-Vialetto-Van Laere syndrome SLC52A3 pontobulbar palsy ataxia;
77.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-1期
- Glutamate receptor ionotropic delta 2 ataxia developmental delay tonic upgaze;
78.X-Linked Lissencephaly With Absent Corpus Callosum and Abnormal Genitalia

机译：X线性缺脑症伴Corp体缺失和生殖器异常
- 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-1期
- XLAG lissencephaly agenesis of the corpus callosum diarrhea pancreatic insufficiency enteroendocrine cells ARX gene congenital intestinal diarrheal diseases;
79.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-1期
- noninvasive ventilation neurologic disease respiratory failure pneumonia neuromuscular disease;
80.Evidence of the Effectiveness of Primary Brachial Plexus Surgery in Infants With Obstetric Brachial Plexus Palsy–Revisited

机译：婴幼儿臂丛神经麻痹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-1期
- Erb’s palsy brachial plexus primary surgery conservative management;
81.Epileptic Negative Myoclonus as the First and Only Symptom in a Challenging Diagnosis of Benign Epilepsy With Centrotemporal Spikes

机译：癫痫阴性肌阵挛是具有挑战性的良性癫痫伴中央颞尖的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-1期
- epileptic negative myoclonus benign epilepsy with centrotemporal spikes VEEG surface EEG;
82.Symptomatic Neonatal Arterial Ischemic Stroke With Prenatal and Postnatal Neuroimaging

机译：产前和产后神经影像学症状性新生儿动脉缺血性卒中
- 作者：Mati Pulver;Kristiina Juhkami;Dagmar Loorits;Pilvi Ilves;Jaanika Kuld;Eve Õiglane-Šlik;Tuuli Metsvaht;Rael Laugesaar
- 期刊名称：《Child Neurology Open》 | 2017年第-1期
- stroke magnetic resonance imaging neuroimaging neonatal seizures seizure;
83.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-1期
- biotin-thiamine-responsive basal ganglia disease biotin-responsive basal ganglia disease thiamine biotin psychological assessment;
84.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
- 期刊名称：《Child Neurology Open》 | 2017年第-1期
- performance monitoring stop-signal task traumatic brain injury pediatrics;
85.CEDNIK

机译：塞尼迪克
- 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-1期
- CEDNIK developmental delay ichthyosis polymicrogyria SNAP29;
86.Rapid Resolution of Enterovirus 71-Associated Opsoclonus Myoclonus Syndrome on Intravenous Immunoglobulin

机译：肠道病毒71相关的视神经管肌阵挛综合征对静脉免疫球蛋白的快速解决
- 作者：Ahmed Sahly;Laurence Gauquelin;Guillaume Sébire
- 期刊名称：《Child Neurology Open》 | 2017年第-1期
- Cerebellitis Neuroinflammation Paraneoplasic Syndrome Glucocorticoids;
87.Distal 22q11.2 Microduplication

机译：远端22q11.2微复制
- 作者：Elana Pinchefsky;Laurence Laneuville;Myriam Srour
- 期刊名称：《Child Neurology Open》 | 2017年第-1期
- developmental delay genetics intellectual disability neurodevelopment pediatric;
88.Implementing a Multidisciplinary Approach to Treating Tuberous Sclerosis Complex

机译：实施多学科治疗结节性硬化症的方法
- 作者：Tanjala T. Gipson;Andrea Poretti
- 期刊名称：《Child Neurology Open》 | 2017年第-1期
- tuberous sclerosis complex seizures neuroimaging pediatric behavior brain tumor;
89.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 Júnior;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-1期
- acute intermittent porphyria anxiety hyponatremia behavior pediatric;
90.Novel LRPPRC Mutation in a Boy With Mild Leigh Syndrome French–Canadian Type Outside of Québec

机译：魁北克省以外的法裔加拿大轻度利氏综合征男孩的新型LRPPRC突变
- 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-1期
- children developmental delay epilepsy metabolism mitochondrial disorder neurodevelopment;
91.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-1期
- mitochondrial mtDNA phenotype genotype fractures osteoporosis;
92.Acute Encephalopathy With Biphasic Seizures and Late Reduced Diffusion Associated With Adenoviral Pneumonia

机译：急性脑病伴双相发作和腺病毒性肺炎相关的晚期扩散减少
- 作者：Keun Soo Lee;Bo Lyun Lee;Young Jin Heo
- 期刊名称：《Child Neurology Open》 | 2019年第-1期
- acute febrile encephalopathy adenovirus seizures;
93.A Rare Case of Bartonella Encephalitis With Hemiplegia

机译：偏瘫巴尔通体脑炎一例
- 作者：Laura Rosas;Kavya Rao;Christine McGough;Ashley Becker
- 期刊名称：《Child Neurology Open》 | 2019年第-1期
- EEG electroencephalogram pediatric adolescents encephalitis Todd paralysis infectious disease cat scratch disease epidemiology;
94.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-乙酰基天冬氨酸减少继发线粒体异常
- 作者：Aneal Khan;Jennifer Bennett;Morris H. Scantlebury;Xing-Chang Wei;Marina Kerr
- 期刊名称：《Child Neurology Open》 | 2019年第-1期
- AIMP1 N-acetylaspartic acid mitochondrial abnormalities seizures;
95.MRI-Negative Myelitis Associated With Myelin Oligodendrocyte GlycoproteinAntibody Spectrum Demyelinating Disease

机译：髓鞘少突胶质细胞糖蛋白相关的MRI阴性脊髓炎抗体谱脱髓鞘疾病
- 作者：Carlos A. Pérez;Stephanie Garcia-Tarodo;Regina Troxell
- 期刊名称：《Child Neurology Open》 | 2019年第-1期
- myelin oligodendrocyte glycoprotein antibody children seizures relapsing myelitis acute demyelinating syndrome;
96.CLIPPERS Spectrum Disorder: A Rare Pediatric Neuroinflammatory Condition

机译：CLIPPERS频谱异常：一种罕见的小儿神经炎症
- 作者：Tarishi Nemani;Anaita Udwadia-Hegde;Purva Keni Karnavat;Ritu Kashikar;Shridhar Epari
- 期刊名称：《Child Neurology Open》 | 2019年第-1期
- Pediatric CLIPPERS Neuro-inflammatory Ataxia Methotrexate;
97.An Exploratory Electrical Stimulation Protocol in the Management of an InfantWith Spina Bifida: A Case Report

机译：婴儿管理中的探索性电刺激协议与Spina Bifida：病例报告
- 作者：Gerti Motavalli;Jan J. McElroy;Gad Alon
- 期刊名称：《Child Neurology Open》 | 2019年第-1期
- Meningomyelocele functional spinal cord electrical stimulation;
98.Doublecortin Mutation in an Adolescent Male

机译：青春期男性中的双皮质素突变
- 作者：Isabelle Zare;Dustin Paul;Shade Moody
- 期刊名称：《Child Neurology Open》 | 2019年第-1期
- neurodevelopment lissencephaly doublecortin neuronal migration;
99.Spinal Cord Diffuse Midline Glioma in a 4-Year-Old Boy

机译：一个4岁男孩的脊髓弥漫性中线神经胶质瘤
- 作者：Ashutosh Kumar;Salman Rashid;Sumit Singh;Rong Li;Leon S. Dure
- 期刊名称：《Child Neurology Open》 | 2019年第-1期
- diffuse midline glioma glioblastoma H3K27M mutation spinal cord disorders pediatrics;
100.De Novo Interstitial Deletion of 9q in a Pediatric Patient With GlobalDevelopmental Delay

机译：从头到尾间质性删除9q患儿全球发展延迟
- 作者：Dennis Keselman;Ram Singh;Ninette Cohen;Zipora Fefer
- 期刊名称：《Child Neurology Open》 | 2019年第-1期
- behavior children developmental delay developmental disability genetics infant intellectual disability mutation neonate pediatric;