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期刊名:Annals of indian academy of neurology

缩写:ANN INDIAN ACAD NEUR

ISSN:0972-2327

e-ISSN:1998-3549

IF/分区:1.8/Q3

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共收录本刊相关文章索引423
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
K Dinkar,Sanjib Sinha,A B Taly et al. K Dinkar et al.
Hashimoto's encephalopathy (H.E.) is probably of autoimmune etiology, and manifests with seizures, stroke-like episodes, cognitive decline, neuropsychiatric symptoms, myoclonus. It is presumed to be autoimmune in origin with high serum tite...
Puneet Mittal Puneet Mittal
Medulloblasoma is a common posterior fossa tumor seen in children and presents with some typical features like midline vermian location and fairly homogeneous enhancment. Desmoplastic variety of medulloblastoma is usually seen in the adults...
Abraham Kuruvilla,Pandurang R Wattamwar Abraham Kuruvilla
We describe a phenomenon of "kinaesthetic extensor plantar response" in advanced pyramidal dysfunction, an interesting observation noted in a patient with dorsal myelopathy. A 44-year-old woman presented with one-year history of gradually p...
Monodeep Biswas,Arghya Chatterjee,Sudip Kumar Ghosh et al. Monodeep Biswas et al.
Background: Rheumatoid arthritis is a multi-system autoimmune disorder predominantly involving multiple small and large joints along with certain extra-articular manifestations. The presence of peripheral neuropathy in pa...
K M Hassan,Prabal Deb,H S Bhatoe K M Hassan
Hypertrophic pachymeningitis (HP) is a rare disorder of diverse etiology. It presents with headaches, cranial neuropathies and ataxia occurring alone or in combination. Dural biopsy is essential to exclude secondary causes of pachymeningiti...
Aparna R Pai,Gopee Krishnan,S Prashanth et al. Aparna R Pai et al.
Background: Global aphasia without hemiparesis (GAWH) is a rare stroke syndrome characterized by the unusual dissociation of motor and language functions. Issues regarding its etio-pathogenesis, lesion sites, and recovery...
Barış Ekici,Yakup Ergül,Burak Tatlı et al. Barış Ekici et al.
Aim: The aim of this work was to assess the respiratory functions of ambulatory Duchenne patients and to propose an earlier time period for intervention. ...
Meral Ozmen,Cengiz Dilber,Burak Tatlı et al. Meral Ozmen et al.
Purpose: Mutations of the α-1 subunit sodium channel gene (SCN1A) cause severe myoclonic epilepsy of infancy (SMEI). To date, over 300 mutations related to SMEI have been described. In the present study, we report new SC...
Rakendra Singh,Manjot Kaur,Deepak Arora Rakendra Singh
Background and objective: The nervous system is the most frequent and serious targets of human immunodeficiency virus (HIV) infection. In spite of a wide prevalence of neurological manifestations in HIV there are not many...