Most Viewed: Last ONE YEAR
  • Review

    Current diagnosis and treatment of cryptococcal meningitis without acquired immunodeficiency syndrome

    Xiao-Su Guo , Hui Bu , Jun-Ying He , Yue-Li Zou , Yue Zhao , Yuan-Yuan Li , Jun-Zhao Cui , Ming-Ming Zheng , Wei-Xin Han , Ze-Yan Zhao
    Cryptococcal meningitis (CM) is a central nervous system infectious disease caused by Cryptococcus. It is the most common fungal infection in the central nervous system, accounting for about 48% of fungal infection. The disease occurs mainly in acquired immunodeficiency syndrome (AIDS) patients and concentrates in the immunocompromised people without AIDS. There are nearly one million new cases of CM each year, and about 70% of them died. In China, CM occurs mainly in people without AIDS and there is an increasing trend in recent years. Early diagnosis and treatment is the key to reducing...
    Published on: 18 Nov 2016
    Views: 25884
    [HTML]   [PDF]  
  • Review

    Necroptosis: a new link between cell death and inflammation

    Yuan-Hang Pan , Xun-Yuan Liu , Jia-Qiang Liu , Qian Liu , Yang Yang , Jia-Lei Yang , Xiu-Fen Zhang , Yin Wu , Ya-Zhou Wang
    Necroptosis is a type of newly identified cell death induced by apoptotic stimuli under conditions where apoptotic execution is prevented. Studies over the past 10 years have revealed the molecular mechanism of necroptosis and challenged the old conception that necrosis is un-programmed. Recently, more and more data have emerged suggesting a close association between necroptosis and inflammation. In this review, the authors summarized the current knowledge of the mechanism of necroptosis, focusing on tumour necrosis factor α induced necroptosis and the roles of necroptosis in regulating...
    Published on: 8 Jul 2016
    Views: 5224
    [HTML]   [PDF]  
  • Topic: Autoimmune neurological diseases associated with autoantibodies specific for synaptic antigens

    Autoimmune encephalopathies in children: diagnostic clues and therapeutic challenges

    Giorgia Olivieri , Ilaria Contaldo , Gloria Ferrantini , Elisa Musto , Roberta Scalise , Maria Chiara Stefanini , Domenica Battaglia , Eugenio Mercuri
    Neuronal surface antibody syndromes (NSAS) encompass a variety of disorders associated with “neuronal surface antibodies”. These share clinical and neuroradiological features that pose challenges related to their recognition and treatment. Recent epidemiological studies show a clear predominance for the glutamate-N-methyl-D-aspartate receptor encephalitis in both adults and pediatric population. Despite this, the overall NSAS’s incidence remains underestimated, and diagnosis persists to be not always easy to achieve. Based on current literature data, in this paper the authors propose a...
    Published on: 8 Jul 2016
    Views: 4534
    [HTML]   [PDF]  
  • Case Report

    Differentiation of radiation necrosis from glioblastoma recurrence after radiotherapy

    Chrissa Sioka , Anastasia Zikou , Anna Goussia , Spyridon Tsiouris , Loucas G. Astrakas , Athanassios P. Kyritsis
    The standard treatment of glioblastoma, the most common type of primary-brain-tumor, involves radiotherapy with concomitant temozolomide chemotherapy. A patient with glioblastoma, post radiotherapy developed magnatic resonance imaging (MRI) changes consistent with either radiation-induced tumor necrosis or tumor recurrence. Perfusion MRI was suggestive of radiation necrosis, but magnetic resonance spectroscopy and 99mTc-Tetrofosmin single photon emission computed tomography was indicative of tumor recurrence. Positron emission tomography scan was not available. Tumor recurrence was...
    Published on: 8 Jul 2016
    Views: 3983
    [HTML]   [PDF]  
  • Editorial

    On the need to unify neuroscience and physics

    Maurits van den Noort , Sabina Lim , Peggy Bosch
    Published on: 26 Dec 2016
    Views: 3608
    [HTML]   [PDF]  
  • Case Report

    Progressive muscle cramps with pain as atypical initial presentations of amyotrophic lateral sclerosis: a case report

    Cheng-Hui Liu , Chi Zhu , Fan Zeng , Heng Yang , Yan-Jiang Wang
    Amyotrophic lateral sclerosis (ALS) is the most common form of motor neuron disease and is a progressive and devastating neurodegenerative disease that affects both lower and upper motor neurons. Muscle cramps, which are characterized by a sudden, painful, involuntary contraction of muscles, are not rare in ALS patients. However, muscle cramps do not normally present early in ALS and therefore not used for the initial diagnosis of ALS. In this paper the authors present a case of ALS with initial manifestation of progressive painful muscle cramps in the absence of muscle weakness. This case...
    Published on: 20 Jul 2016
    Views: 2858
    [HTML]   [PDF]  
  • Original Article

    Symptom severity, quality of sleep, and treatment adherence among patients suffering from schizophrenia and depression

    Peggy Bosch , Janina Waberg , Maurits van den Noort , Heike Staudte , Sabina Lim , Jos Egger
    Aim: Treatment non-adherence is a common problem in patients suffering from schizophrenia and depression. This study investigated the possible relationships between symptom severity, quality of sleep, and treatment adherence. Methods: Thirty outpatients with schizophrenia and 58 outpatients with depression were enrolled in this study. The beck depression Inventory-II, the positive and negative syndrome scale, and the pittsburgh sleep quality index were used to assess symptom severity and quality of sleep, and sleep log data were used to measure treatment adherence. Results: The preliminary...
    Published on: 20 May 2016
    Views: 2835
    [HTML]   [PDF]  
  • Review

    Neurological manifestations in Fabry disease

    Joseph Bruno Bidin Brooks , Yara Dadalti Fragoso
    Fabry disease (FD) is a rare, progressive, multisystem and highly debilitating disease. FD is an X-linked lysosome storage disorder that results in α-galactosidase A deficiency. The subsequent accumulation of glycosphingolipids is more evident in vascular endothelium and smooth-muscle cells. The resulting effect of the deposition is generalized inflammation and vasculopathy, which can also affect the central and peripheral nervous system. FD progresses with kidney dysfunction, angiokeratoma of the skin, cardiomyopathy, cerebrovascular events and neurological disorders. In the present...
    Published on: 28 Oct 2016
    Views: 2774
    [HTML]   [PDF]  
  • Case Report

    Huge supratentorial cortical ependymoma in a young child: case report and literature review

    Mehdi Darmoul , Mohamed Kilani , Atef Ben Nsir , Mohamed Nejib Hattab
    Supratentorial cortical ependymomas are uncommon in the pediatric population and extremely rare in very young children. Histologically, tumors of the anaplastic type are also less common in children. The authors report one case of anaplastic cortical ependymoma in a 16-month-old girl who presented with a 7-day history of left side weakness and rapid neurological deterioration. Brain imaging with computed tomography and magnetic resonance imaging scanning showed a huge right fronto-parietal cystic and solid lesion compressing the brain parenchyma. The young child was operated via a...
    Published on: 20 Jun 2016
    Views: 1940
    [HTML]   [PDF]  
  • Review

    Statins in acute neurologic disease: which one, which dose, when to start, and when not to stop

    Bong-Su Kang , Gene Sung , May Kim-Tenser , Nerses Sanossian
    Statins could have physiologic properties that may benefit patients that have been diagnosed with various acute neurological diseases. This review aims tosummarize the literature pertaining to stain use in acute neurological disease such as subarachnoid hemorrhage, intracerebral hemorrhage (ICH), cerebral ischemia (CI), traumatic brain injury, status epilepticus and meningitis. The authors reviewed published abstracts and manuscripts pertaining to experimental and clinical trials relevant to statins in acute neurological disease. Although acute statin therapy in the setting of subarachnoid...
    Published on: 20 Jun 2016
    Views: 1936
    [HTML]   [PDF]  
  • Original Article

    Inhibition and reversal of growth cone collapse in adult sensory neurons by enteric glia-induced neurotrophic factors

    Simon Feng , Kiran Reddy , Cai-Xin Su , Shu-Cui Jiang
    Aim: Previous studies show enteric glia (EG)-conditioned medium promotes neurite outgrowth in adult dorsal root ganglia (DRG) derived sensory neurons. This EG-conditioned medium contains various neurotrophic factors, including nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), glial cell line-derived neurotropic factor (GDNF), and neurotrophin-3 (NT-3). This study attempts to determine the importance of these neurotrophic factors in enabling DRG-derived sensory neuron axons to overcome the inhibitory guidance cues released from the glial scar. Methods: A Semaphorin 3A...
    Published on: 31 Aug 2016
    Views: 1674
    [HTML]   [PDF]  
  • Case Report

    Good recovery of a patient with neurocysticercosis using two antihelminthic drugs combined with steroid

    Xin-Di Li , Hua-Bing Wang , Heng Zhou , An-Na Zhou , Lin Zhao , Yong-Hong Liu , Xiao-Qing Gong , Xing-Hu Zhang
    Neurocysticercosis is the most common parasitic infection of the central nervous system. We present a case report of a neurocysticercosis patient with multiple cysts, who presented with new onset generalized tonic-clonic seizures. A 4-cycle treatment of 2 different antihelminthic drugs with dexamethasone and sodium valproate led to clinical improvement without any adverse reactions. The manifestations of neurocysticercosis are protean and the diagnosis should be considered whenever multiple cysts are seen on computed tomography or magnetic resonance imaging. The antihelminthic treatment of...
    Published on: 20 May 2016
    Views: 1508
    [HTML]   [PDF]  
  • Review

    Current and emerging therapies for neuromyelitis optica

    Cong Zhao , Hong-Zeng Li , Ya-Nan Bai , Zhu-Yi Li , Jun Guo
    Neuromyelitis optica (NMO) is an autoimmune demyelinating disease that mainly affects the optic nerve and spinal cord, potentially resulting in blindness and paralysis. Once thought to be a clinical variant of multiple sclerosis, NMO is currently considered as a different disease with its own features due to the identification of a specific autoantibody against aquaporin 4. Given the high risk of disability, treatment should be launched once the diagnosis is established. Evidence from clinical practice showed that traditional immunosuppressive agents affecting the function of T and B cells...
    Published on: 20 Jun 2016
    Views: 1374
    [HTML]   [PDF]  
  • Review

    Immune-to-brain signaling and substrates of altered behavior during inflammation

    Jan Pieter Konsman
    During the systemic inflammatory response to acute infection, and when in a safe environment, endothermic mammals typically display reduced activity and food intake, increased sleep, and the adoption of a curled-up position. These changes in behavior, in concert with fever, are adaptive in that they contribute to host survival. The present review addresses the immune-to-brain signaling pathways as well as possible neural substrates mediating reduced exploration and food intake during acute systemic inflammation. These involve rapid activation of peripheral nerves and glutamatergic brainstem...
    Published on: 26 Sep 2016
    Views: 1321
    [HTML]   [PDF]  
  • Commentary

    Sex differences in Alzheimer’s disease

    Yi Xing
    Recently, Koran et al.[1] published an article, named “Sex differences in the association between Alzheimer’s disease (AD) biomarkers and cognitive decline” in Brain Imaging and Behavior. The result proved that there were sex-specific associations between biomarkers of AD. This article added evidence to the theory of sex differences in AD.
    Published on: 8 Jul 2016
    Views: 1183
    [HTML]   [PDF]  
  • Case Report

    A case of Hashimoto's encephalopathy presenting with seizures and cognitive impairment

    Xing-Yong Chen , Yin-Zhou Wang , Hui-Xin Lei , Xu Zhang
    Hashimoto's encephalopathy (HE) is a rare disease with unknown pathogenesis. An epileptic seizure is reported in association with HE. Here, the author reported an 18-year-old girl with a history of hyperthyroidism for one year. She was admitted to the hospital due to status epilepticus. Serum thyroid function test showed that the concentration of anti-thyroid peroxidase antibodies and thyroglobulin antibody were significantly elevated. Brain magnetic resonance imaging showed that multiple abnormalities varied from bilateral frontal, parietal, occipital-temporal lobe to cerebellum...
    Published on: 20 May 2016
    Views: 1156
    [HTML]   [PDF]  
  • Case Report

    Takayasu’s arteritis - aphasia as an initial presentation

    Davinder Singh Rana , Anuradha Batra , Ish Anand , Samir Patel , Pooja Gupta
    Takayasu arteritis (TA) is an uncommon disease of young women, characterized by granulomatous vasculitis of medium and large arteries. Neurological involvement is reported in only a minority of patients and occurrence of neurological syndromes as the first manifestation of disease has been rarely reported. We present clinical, laboratory and imaging findings of a 40 years old lady with TA, who initially presented with clinical manifestations of stroke in form of aphasia. The rarity of the disease and especially such a presentation can cause considerable delay in the diagnosis and treatment.
    Published on: 31 Aug 2016
    Views: 1109
    [HTML]   [PDF]  
  • Case Report

    Status epilepticus in scleromyxedema

    Sofia Markoula , Sofia Zouroudi , Sotirios Giannopoulos , Kimon Tsoukanelis , Ananstasia Zikou , Athanassios P. Kyritsis
    Scleromyxedema is a rare dermatologic disorder, characterized by erythematous or yellowish lichenoid waxy papules. Neurological manifestations are rare but well-recognized. A 51-year-old woman, diagnosed with scleromyxedema, was admitted to the hospital with status epilepticus, caused by brain lesions, as disclosed in a brain magnetic resonance imaging (MRI). The patient was treated with anticonvulsants and corticosteroids and gradually recovered fully. A complete remission of the lesions was shown in a follow-up brain MRI. In cases with scleromyxedema and the presence of neurological...
    Published on: 20 May 2016
    Views: 1100
    [HTML]   [PDF]  
  • Case Report

    A case report of acute pediatric bacterial meningitis due to the rare isolate, Pseudomonas putida

    Grishma V. Kulkarni
    Acute bacterial meningitis (ABM) is the medical emergency which warrants an early diagnosis and an aggressive therapy. Despite the availability of the potent newer antibiotics, the mortality caused by ABM and its complications remain high in India, ranging from 16% to 32%. The aim of this case report is to present the rare isolation of Pseudomonas putida from cerebrospinal fluid sample. Besides this, the author also emphasizes the importance of correctly identifying the organism and thus the selection of the most accurate antibiotic from the susceptibility profile to allow for early...
    Published on: 26 Sep 2016
    Views: 1073
    [HTML]   [PDF]  
  • Editorial

    Interleukin-1beta: a common thread between inflammation, pain and opioid tolerance

    Shekher Mohan
    Published on: 26 Sep 2016
    Views: 1066
    [HTML]   [PDF]  
Quick Links
  • OAE Publishing Inc. (OAE) is an online open-access publisher specializing in the publication of biomedical peer-reviewed journals...

  • Contact us
  • Leave feedback
Partners
Copyright © 2017 OAE Publishing Inc. All Rights Reserved.