Tardive Meige's syndrome associated with olanzapine.

abstract：Objectives:Stress, anxiety, and depression are known to be associated with the development of neurodegenerative disorders through interactions with the underlying pathophysiology. We hypothesized that the presence of these symptoms contributes to cognitive disturbances and dementia in Parkinson's disease (PD). The pres...

journal_title：Annals of Indian Academy of Neurology

authors： Pal A,Pegwal N,Behari M,Sharma R

更新日期：2019-10-01 00:00:00

abstract：:Leigh syndrome (LS) is a heterogeneous familial or sporadic neurodegenerative disorder. It is typically seen in infancy or childhood, although rare cases of adult onset have been described. The authors describe a 37-year-old woman who presented with protracted gastrointestinal symptoms followed by acute brain stem syn...

journal_title：Annals of Indian Academy of Neurology

authors： Jabeen SA,Sandeep G,Mridula KR,Meena AK,Borgohain R,Sundaram C

更新日期：2016-01-01 00:00:00

abstract：:Stroke is a major health problem world-wide and its burden has been rising in last few decades. Until now tissue plasminogen activator is only approved treatment for stroke. Angiogenesis plays a vital role for striatal neurogenesis after stroke. Administration of various growth factors in an early post ischemic phase,...

journal_title：Annals of Indian Academy of Neurology

authors： Talwar T,Srivastava MV

更新日期：2014-01-01 00:00:00

abstract：OBJECTIVE:There is paucity of reports on thyrotoxic periodic paralysis (TPP) from India. We report the patients with TPP and compare them with idiopathic hypokalemic periodic paralysis (IHPP). MATERIALS AND METHODS:Patients with hypokalemic periodic paralysis (HPP) treated during the past 11 years were evaluated retro...

journal_title：Annals of Indian Academy of Neurology

authors： Kalita J,Goyal G,Bhoi SK,Chandra S,Misra UK

更新日期：2012-07-01 00:00:00

abstract：Background:Stroke results in significant caregiver burden and strain. Objective:The main objectives of this study is to assess the burden and its consequences in caregivers of stroke patients and to determine the associated factors to caregivers' burden. Methods:A cross-sectional study was conducted over 1 year on 70...

journal_title：Annals of Indian Academy of Neurology

authors： Mandowara B,Patel AN,Amin AA,Phatak A,Desai S

更新日期：2020-01-01 00:00:00

abstract：CONTEXT:The guideline recommended dose of intravenous (i.v) recombinant tissue-type plasminogen activator (rt-PA) for acute ischemic stroke is 0.9 mg/kg in the European and American populations. In Asiatic population, some studies have shown that a lower dose of i.v rt-PA is equally efficacious. AIMS:To assess if ther...

journal_title：Annals of Indian Academy of Neurology

authors： Abraham SV,Thaha F,Krishnan SV,Shajan A,Balakrishnan JM,Palatty BU

更新日期：2017-01-01 00:00:00

abstract：:Chronic relapsing inflammatory optic neuropathy (CRION) is a recently described recurrent optic neuropathy which is steroid responsive. Several features distinguish this entity from optic neuritis associated with demyelinating disorders and connective tissue diseases. The severe degree of visual loss, persistence of p...

journal_title：Annals of Indian Academy of Neurology

authors： Saini M,Khurana D

更新日期：2010-01-01 00:00:00

abstract：:Pursuing a diagnosis despite a negative nerve biopsy report requires a strong clinical conviction. Paying attention to clinical details and a diligent review of medical records is needed to solve cases in which the diagnosis is not obvious despite numerous tests. We present once such case of an elderly man with chroni...

journal_title：Annals of Indian Academy of Neurology

authors： Kharadi M,Harsha SV,Gopalakrishnan G,Karthick GA,Raj V,Kannan S

更新日期：2016-10-01 00:00:00

abstract：:The case of an 82-year-old female with probable Alzheimer's disease (AD), who developed unusual artistic creativity after development of her disease, is described. The possible pathogenetic mechanism is discussed. The patient showed no inclination toward visual arts during her premorbid years. However, 4 years after d...

journal_title：Annals of Indian Academy of Neurology

authors： Chakravarty A

更新日期：2011-10-01 00:00:00

abstract：:During the colloquium on drug-resistant epilepsy (DRE) at National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore on August 16-18, 2013, a number of presentations were made on the surgically remediable lesional epilepsy syndromes, presurgical evaluation, surgical techniques, neuropathology of drug r...

journal_title：Annals of Indian Academy of Neurology

authors： Rao MB,Arivazhagan A,Sinha S,Bharath RD,Mahadevan A,Bhat M,Satishchandra P

更新日期：2014-03-01 00:00:00

abstract：Introduction:Serotonin syndrome (SS) is a drug-induced clinical syndrome that results from the excess intrasynaptic concentration of serotonin. Prospective observations are limited for SS. Methods:We prospectively recruited 45 consecutive adult patients (>18 years) fulfilling the Hunter's criteria for SS. All patients...

journal_title：Annals of Indian Academy of Neurology

authors： Prakash S,Rathore C,Rana KK,Dave A,Joshi H,Patel J

更新日期：2019-01-01 00:00:00

abstract：Background:Stroke survivors suffer from significant neuropsychiatric disturbances and these disturbances act as barrier in the motor recovery. Medication is the common treatment but it has adverse effects. Hence, there is a need to find out effective treatments with or without minimal side effects for gross motor recov...

journal_title：Annals of Indian Academy of Neurology

authors： Bhardwaj M,Arumugam N,Gambhir S

更新日期：2018-07-01 00:00:00

abstract：BACKGROUND:Congenital myopathies (CMs) though considered distinct disorders, simultaneous occurrence of central nucleus, nemaline rods, and cores in the same biopsy are scarcely reported. OBJECTIVE:A retrospective reassessment of cases diagnosed as CMs to look for multiple pathologies missed, if any, during the initia...

journal_title：Annals of Indian Academy of Neurology

authors： Dhinakaran S,Kumar RS,Thakkar R,Narayanappa G

更新日期：2016-04-01 00:00:00

abstract：:Takayasu's arteritis is a chronic, idiopathic, inflammatory disease primarily affecting aorta and its branches. It mainly affects young females in the age group of 10-30 years. Various atypical presentations of Takayasu's arteritis have been described in children. These atypical presentations can cause delayed diagnos...

journal_title：Annals of Indian Academy of Neurology

authors： Zaki SA,Chavan V,Shanbag P

更新日期：2011-07-01 00:00:00

abstract：:Neuromyelitis optica is an inflammatory demyelinating disorder of the central nervous system. The discovery of a specific antibody (NMO IgG /aquaporin-4 antibody) in patients with this condition has led to a marked revival of research on the disease. This article summarizes the major advances in neuromyelitis optica, ...

journal_title：Annals of Indian Academy of Neurology

authors： Jacob A

更新日期：2009-10-01 00:00:00

abstract：:The nosology, classification and pathophysiology of ophthalmoplegic migraine (OM) remains complex and debatable. A recently proposed classification of OM leaves several caveats. A critical analysis of all reported cases of OM (1993-2010) has been made incorporating the authors' own experience to arrive at a simple, un...

journal_title：Annals of Indian Academy of Neurology

authors： Chakravarty A,Mukherjee A

更新日期：2012-08-01 00:00:00

abstract：:Multiple sulfatase deficiency is biochemically characterized by the accumulation of sulfated lipids and acid mucopolysaccharides. The gene sulfatase-modifying factor 1 (SUMF1), recently identified, encodes the enzyme responsible for post-translational modification of a cysteine residue, which is essential for the acti...

journal_title：Annals of Indian Academy of Neurology

authors： Incecik F,Ozbek MN,Gungor S,Pepe S,Herguner OM,Mungan NO,Gungor S,Altunbasak S

更新日期：2013-10-01 00:00:00

abstract：BACKGROUND:Only few papers have investigated the impact of multiple sclerosis (MS), especially MS-related fatigue and the impact of the quality of sleep on the quality of life (QoL) in MS patients. OBJECTIVE:The objective of this study was to measure the quality of life in MS patients and the impact of disability, fat...

journal_title：Annals of Indian Academy of Neurology

authors： Ghaem H,Borhani Haghighi A

更新日期：2008-10-01 00:00:00

abstract：:Fazio Londe Syndrome is a rare neurological disorder presenting with progressive bulbar palsy with respiratory failure. Initially considered to have an unrelenting course, is now found to be due to mutations in the SLC52A3 gene which encodes the intestinal (hRFT2) riboflavin transporter in some children. We report an ...

journal_title：Annals of Indian Academy of Neurology

authors： Varadarajan P,Thayanathi V,Pauline LC

更新日期：2015-01-01 00:00:00

abstract：INTRODUCTION:Neurologists in their clinical practice are faced with inquiries about the suitability of stem cell approaches by patients with a variety of acute and chronic (namely neurodegenerative) disorders. The challenge is to provide these patients with accurate information about the scope of stem cell use as well ...

journal_title：Annals of Indian Academy of Neurology

authors： Devi MG,Sharma A,Mohanty S,Jain N,Verma K,Padma MV,Pal P,Chabbra HS,Khadilkar S,Prabhakar S,Singh G

更新日期：2016-07-01 00:00:00

abstract：OBJECTIVES:The purpose of this study was to investigate Iintra-rater reliability of the Modified Tardieu Scale (MTS) in elbow flexors and ankle plantar flexors in adult subjects with stroke. MATERIALS AND METHODS:A total of 91 subjects with stroke participated in this test-retest study. Intra-rater reliability of the ...

journal_title：Annals of Indian Academy of Neurology

authors： Singh P,Joshua AM,Ganeshan S,Suresh S

更新日期：2011-01-01 00:00:00

abstract：:Kleine-Levin syndrome (KLS) is a rare sleep disorder mainly affecting teenage boys in which the main features are intermittent hypersomnolence, behavioral and cognitive disturbances, hyperphagia, and in some cases hypersexuality. Each episode is of brief duration varying from a week to 1-2 months and affected people a...

journal_title：Annals of Indian Academy of Neurology

authors： Ramdurg S

更新日期：2010-10-01 00:00:00

abstract：:Headache is the most common symptom of cerebral venous thrombosis (CVT); however, the detailed underlying mechanisms and characteristics of headache in CVT have not been well described. Here, we report two cases of CVT whose primary and lasting presentation was orthostatic headache, suggestive of decreased intracrania...

journal_title：Annals of Indian Academy of Neurology

authors： Kim JB,Kwon DY,Park MH,Kim BJ,Park KW

更新日期：2013-01-01 00:00:00

abstract：:A 60-year-old male with chronic lymphatic leukemia (CLL) after 6 months of fludarabine therapy was admitted with status epilepticus and developed left hemiplegia. His magnetic resonance imaging revealed multiple T2 hyperintense lesions in the right frontal and left parieto-occipital lesion, simulating progressive mult...

journal_title：Annals of Indian Academy of Neurology

authors： Kalita J,Patel NS,Misra UK

更新日期：2008-04-01 00:00:00

abstract：OBJECTIVE:Frontal executive dysfunction (FED) and abnormalities in volumetric magnetic resonance imaging (MRI) have been described in juvenile myoclonic epilepsy (JME). We aimed to compare JME patients with and without FED by group analysis of voxel-based morphometric (VBM) estimates of brain volume in MRI. SUBJECTS A...

journal_title：Annals of Indian Academy of Neurology

authors： Pillai SH,Raghavan S,Mathew M,Gopalan GM,Kesavadas C,Sarma S,Thomas SV

更新日期：2017-07-01 00:00:00

abstract：:Opercular myoclonic-anarthric status epilepticus (OMASE) is an uncommon disorder of diverse etiology. This condition is characterized by fluctuating cortical dysarthria associated with epileptic myoclonus involving glossopharyngeal musculature bilaterally. We report two cases of OMASE of vascular etiology in adults. I...

journal_title：Annals of Indian Academy of Neurology

authors： Bhaskara Rao JV,Vengamma B,Naveen T,Rao MS

更新日期：2013-10-01 00:00:00

abstract：:Cerebrotendinous xanthomatosis is an autosomal recessive inborn error of metabolism that is an often missed but treatable cause of hereditary ataxia. We report a case of cerebrotendinous xanthomatosis (CTX) that was diagnosed only after the development of cognitive decline and adult onset ataxia in a 35-year-old man. ...

journal_title：Annals of Indian Academy of Neurology

authors： Shaji B,Srikumar B,Ramachandran D

更新日期：2019-10-01 00:00:00

abstract：:This cross-sectional case control study included subjects aged between 18 and 65 years with diagnosis of myasthenia gravis (MG) in Osserman's Stage I and Stage IIa and those in remission with positive and negative acetylcholine receptor antibody (AChRAb). They were evaluated for heart rate variability (HRV) and other ...

journal_title：Annals of Indian Academy of Neurology

authors： Puneeth CS,Chandra SR,Yadav R,Sathyaprabha TN,Chandran S

更新日期：2013-07-01 00:00:00

abstract：Background and Aims:Intracranial atherosclerotic disease (ICAD) is common in the Asian population, but less studied in South Asians compared to East Asians. We compared risk factors, treatments, and outcomes among consecutive patients with symptomatic ICAD from India with a mixed-ethnic cohort from Chicago, Illinois. ...

journal_title：Annals of Indian Academy of Neurology

authors： Saraf U,Prabhakaran S,Arun K,Babiker A,Rajendran A,Kesavadas C,Sylaja PN

更新日期：2020-05-01 00:00:00

abstract：:Limbic encephalitis (LE) is a neurological syndrome that may present in association with cancer, infection, or as an isolate clinical condition often accompanying autoimmune disorders. LE associated with glutamic acid decarboxylase antibodies (anti-GAD) is rare in children. Here, we characterized the clinical and labo...

journal_title：Annals of Indian Academy of Neurology

authors： Incecik F,Hergüner OM,Yıldızdaş D,Horoz O,Besen S

更新日期：2015-04-01 00:00:00