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Pediatric Neurology
(Pediatr Neurol) 《小儿神经病学》

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小儿神经病学
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《小儿神经病学》杂志发表最新的同行评议的临床和研究文章,涉及神经系统发育的各个方面。

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Published 2013年1月,Volume 48,Issue 1

最新一期


Article TitleAuthor(s)Pages
Introduction of the New Editor-in-Chief of Pediatric Neurology

Kenneth F. Swaiman1
Passing the Torch

E. Steve Roach2
Review Articles
Article TitleAuthor(s)Pages
Hyperbilirubinemia: Subcortical Mechanisms of Cognitive and Behavioral Dysfunction

Leonard F. Koziol, Deborah Ely Budding, Dana Chidekel3-13
Mechanisms of Pediatric Cerebral Arteriopathy: An Inflammatory Debate

Aleksandra Mineyko, Adam Kirton14-23
Original Articles
Article TitleAuthor(s)Pages
Diffusion Tensor Imaging of Sports-Related Concussion in Adolescents

Naznin Virji-Babul, Michael R. Borich, Nadia Makan, Tiffany Moore, et al.24-29
Childhood Tubercular Meningitis: An Institutional Experience and Analysis of Predictors of Outcome

Altaf Ramzan, Khursheed Nayil, Rouf Asimi, Abrar Wani, et al.30-35
Genetic Risk Factors for Perinatal Arterial Ischemic Stroke

Amy A. Gelfand, Lisa A. Croen, Anthony R. Torres, Yvonne W. Wu36-41
Treatment Outcomes of West Syndrome in Infants With Down Syndrome

Oranee Sanmaneechai, Yoshimi Sogawa, Wendy Silver, Karen Ballaban-Gil, et al.42-47
Pontocerebellar Hypoplasia in Extreme Prematurity: Clinical and Neuroimaging Findings

Dimitrios I. Zafeiriou, Athina Ververi, Athanasia Anastasiou, Vasiliki Soubasi,et al.48-51
Predictors of Intractable Childhood Epilepsy

Berna Seker Yilmaz, Cetin Okuyaz, Mustafa Komur52-55
Case Reports
Article TitleAuthor(s)Pages
Early Fetal Development of the Anterior Commissure

Kwang Ho Cho, Gen Murakami, Jose Francisco Rodríguez-Vázquez56-58
Congenital Hypomyelinating Neuropathy Attributable to a De Novo p.Asp61Asn Mutation of the Myelin Protein Zero Gene

Takahiro Yonekawa, Hirofumi Komaki, Yuko Saito, Hiroshi Takashima, et al.59-62
Novel KCNQ2 Mutation in a Large Emirati Family With Benign Familial Neonatal Seizures

Imad Y. Saadeldin, Reham M. Milhem, Lihadh Al-Gazali, Bassam R. Ali63-66
Leigh Syndrome in a Girl With a Novel DLD Mutation Causing E3 Deficiency

Shane C. Quinonez, Steven M. Leber, Donna M. Martin, Jess G. Thoene, et al.67-72
Cutaneous and Leptomeningeal Hemangiomas With Impressive Benign Evolution

Raffaele Falsaperla, Piero Pavone, Martino Ruggieri, Lorenzo Pavone73-75
Isolated Leptomeningeal Enhancement in Tacrolimus-Associated Posterior Reversible Encephalopathy Syndrome

Ryan T. Fitzgerald, Joana Osorio, Ashok Panigrahy, George V. Mazariegos, et al.76-78
Correspondence
Article TitleAuthor(s)Pages
Subcutaneous Route for Refractory Epilepsy

Luis Ignacio Gonzalez-Granado, Rogelio Simon, Ana Camacho-Salas79
Response

Uri Kramer79
Calendar
Article TitleAuthor(s)Pages
Calendar

80
Frontmatter
Article TitleAuthor(s)Pages
Table of Contents

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