国际在线医疗理事会(IOMC)| 医学研究

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摘要/索引于

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案例报告

Traumatic Anterior Dislocation of the Knee Without Any Neurovascular Complication-Case Report

Nitesh Gahlot, Uttam Chand Saini and Smeer Aggarwal

We are reporting a case of traumatic anterior dislocation of the left knee without any neurovascular complication. To our knowledge, such complete dislocation without involvemen..查看更多»

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Substantia Nigra Hyperechogenicity for the Early Detection of Parkinson's Disease

Rezzak Yilmaz and Daniela Berg

Hyperechogenicity of the substantia nigra (SN+) is an imaging marker which may be detected in individuals at risk for Parkinson’s disease (PD). In this short commentary, t..查看更多»

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Long Non-coding RNAs Expression in Renal Cell Carcinoma

Mohammad Taheri, Mir Davood Omrani, Soudeh Ghafouri-Fard

Renal cell carcinoma (RCC) is among common cancers of the urogenital system. Several cancer-related pathways have been shown to be implicated in its pathogenesis. More recently,..查看更多»

摘要

The decision-making process in orthodontics: To extract or not to extract?

Omar El Bayoumy

The major consideration in this important decision relates to management of crowding/ protrusion and the possibility of camouflage for skeletal problems. Crowding/Protrusion. If..查看更多»

简短的沟通

"Prognostic importance of high-sensitivity C-reactive protein (hs-CRP) for in-stent restenosis and 6-month major adverse cardiac events following percutaneous coronary intervention (PCI)"

Alireza Rai, Hashem kazerani, Farid Najafi, Zahra Jalili, Marzieeh Assareh, Syrus Jalili, MohaamadJavad Shams, Mostafa Bahremand, MohammadReza Saidi, Nahid Salehi, Hooman Kazemi

"There is controversy regarding the prognostic role of high-sensitivity C-reactive protein (hs-CRP) in predicting re-stenosis and major adverse cardiac events (MACE) in pat..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»