国际在线医疗理事会(IOMC)| 医学研究

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抽象的

2020 Conference Announcement: 3rd World Neurone Congress

Rajendra D. Badgaiyan

A recent research in Neuron and Neurology has been increased in the global market. The biotechnologists, cell biologist’s showcase is ready to develop at an enduring rate ..查看更多»

研究文章

Glasgow Coma Scale, Brain Computerized Tomography and Neurophysiological Methods as Prognostic Factors of Pediatric Coma

Mohammad W. El-Anwar, Waleed M. Ibrahim, Sanaa M. Abdel Salam, Safaa H.A. Saleh, Mohammad A. Zeidan and Moanes A. Enaba

Background and objectives: Coma is characterized by the total absence of both arousal and awareness. The outcome of coma depends on the etiology, depth and..查看更多»

简短的沟通

Neurocognitive Development through Systematic Knowledge Compilation among Young Adults

Kerstin Wentz and Trevor Archer

According to The National Board of Health and Welfare in Sweden almost 190.000 children and young adults suffer from mental illness. Between 2006 and 2016 there was also a 70 pe..查看更多»

研究文章

The Responses of Korean Society during 2015 South Korean MERS outbreak

Hyun Sook Jo, Sung Eun Yi*, Chung Sook Kim, Jeong Mo Park, Mi Jin Shin and Hyang Soon Oh

Purpose: The purpose of this study is to find what was the social responses and to identify the failure and weakness in 2015 MERS control in South Korea, and to..查看更多»

研究文章

Effects of IgM Anti-Galnac-GD1a Monoclonal Antibody on Neuromuscular Transmission and Calcium Channel Binding in the Rat Neuromuscular Junction

Sayako Hotta, Takumi Nagaoka, Yoshihiko Nakatani, Toshie Kambe, Kenji Abe, Yutaka Masuda, Iku Utsunomiya and Kyoji Taguchi

Guillain-Barré syndrome with antibodies against ganglioside N-acetylgalactosaminyl GD1a (GalNAc-GD1a) is
characterized by a rapid onset of predominantly distal pur..查看更多»

案例报告

Neonatal Seizures do not Exclude Dravet Syndrome Diagnosis

Elzbieta Szczepanik, Iwona Terczynska, Dorota Antczak-Marach, Paulina Gorka-Skoczylas and Dorota Hoffman-Zacharska

Introduction: We present a patient with Dravet syndrome (DS) caused by the SCN1A mutation, and with neonatal seizure history.
Material and Method..查看更多»