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Annals of Indian Academy of Neurology

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https://www.readbyqxmd.com/read/30532377/florid-nonmotor-manifestations-of-a-pathologically-proven-progressive-supranuclear-palsy
#1
Chaewon Shin, Sung-Hye Park, Aryun Kim, Tae-Beom Ahn
No abstract text is available yet for this article.
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532376/scapular-fracture-as-isolated-manifestation-of-charcot-neuroarthropathy-in-syringomyelia
#2
Mansoor C Abdulla, Reas Ali Aryadan, Haniyya
No abstract text is available yet for this article.
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532375/-lost-my-way-transient-topographic-amnesia-a-bizarre-manifestation-of-migraine
#3
Doris George Yohannan, Ranjit Sanu Watson, Neelankavil Jose John
No abstract text is available yet for this article.
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532374/antineutrophil-cytoplasmic-antibody-vasculitis-causing-skull-base-inflammation-and-aortitis
#4
Boby Varkey Maramattom, Joe Thomas, Shagos Nair
No abstract text is available yet for this article.
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532373/hereditary-spastic-paraplegia-type-35-with-a-novel-mutation-in-fatty-acid-2-hydroxylase-gene-and-literature-review-of-the-clinical-features
#5
Faruk Incecik, Seyda Besen, Sevcan Tug Bozdogan
No abstract text is available yet for this article.
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532372/curing-neurophobia-a-feasible-suggestion-for-low-resource-settings
#6
V Dinesh Kumar
No abstract text is available yet for this article.
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532371/polymyositis-with-too-many-associations-a-paraneoplastic-syndrome
#7
Arunmozhimaran Elavarasi, Venugopalan Y Vishnu, M V Padma Srivastava, Vinay Goyal, Mamta Bhushan Singh, Gaurav Khanna, Vaishali Suri, Mehar Chand Sharma
No abstract text is available yet for this article.
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532370/masking-of-papilledema-by-glaucoma
#8
Nataraja Pillai Venugopal, Sherin Kummararaj, Govindaraj Kummararaj
No abstract text is available yet for this article.
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532369/wernicke-encephalopathy-with-atypical-findings-on-magnetic-resonance-imaging
#9
Kiran Kumar Ramineni, Sravan Kumar Marupaka, Ravikanth Jakkani, Abhijeet Ingle
No abstract text is available yet for this article.
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532368/nine-syndrome-case-report-and-review-of-clinical-signs-in-internuclear-ophthalmoplegia
#10
Jennifer Singhdev, Ajay Asranna, Sachin Sureshbabu, Gaurav Kumar Mittal, Sweta Singla, Sudhir Peter, Sobhana Chindripu
The pathologic involvement of brainstem and midbrain nuclei and white matter tracts in various combinations may result in a spectrum of arithmetically derived syndromes. They include 'one and a half syndrome', 'eight and a half syndrome' and 'fifteen and a half syndrome'. We report a case of 'nine syndrome', which has been reported more recently, caused by caused by acute pontine infarcts and characterised clinically by a combination of internuclear ophthalmolplegia, ipsilateral horizontal gaze palsy, lower motor neuron type of facial palsy, contralateral hemiparesis and hemianesthesia...
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532367/improvement-in-obsessive-compulsive-disorder-following-right-anterior-temporal-lobectomy-and-amygdalohippocampectomy-in-a-patient-with-refractory-temporal-lobe-epilepsy-with-right-mesial-temporal-sclerosis
#11
A S Shreedhara, G K Bhargava, Raghavendra Kenchaiah, C M Ravindranadh, Arivazhagan Arima, Rose Dawn Bharath, Jitender Saini, N Chandana, Jamuna Rajeswaran, Malla Bhaskara Rao, Parthasarathy Satishchandra, Y C Janardhana Reddy, Sanjib Sinha
There are reports of co-occurrence of obsessive-compulsive disorder (OCD) in patients with temporal lobe epilepsy (TLE). We present a report of a patient with refractory TLE due to hippocampal sclerosis with concomitant OCD on pharmacotherapy for both. She underwent surgery for standard anterior temporal lobectomy with amygdalohippocampectomy and reported improvement in obsessive-compulsive symptoms subsequently. We seek to further evidence of interaction between the two conditions and argue to undertake future research exploration on the same...
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532366/central-and-peripheral-nervous-system-involvement-in-a-patient-with-scrub-infection
#12
Atul Phillips, Gautam Rai Aggarwal, Vishal Mittal, Gurpreet Singh
Scrub infection is an important differential of undifferentiated febrile illness in the subtropical and tropical countries. Neurological complications of scrub infection have a varied spectrum of presentation involving both the central nervous system, among which meningitis and meningoencephalitis are the most common presentations. The peripheral nervous system manifestations include Guillain-Barre syndrome (GBS) is not commonly reported. The coexistence of both central and peripheral involvement is rare, and we would like to report a case of a patient who was diagnosed with scrub infection and presented with meningoencephalitis and later developed GBS in the course of the disease on treatment for scrub infection...
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532365/simultaneous-occurrence-of-axonal-guillain-barr%C3%A3-syndrome-in-two-siblings-following-dengue-infection
#13
Shweta Pandey, Ravindra Kumar Garg, Hardeep Singh Malhotra, Neeraj Kumar, Ravi Uniyal
Guillain-Barré syndrome (GBS) is an infrequent neurological complication of dengue viral infection. It is broadly divided into either acute inflammatory demyelinating variety or an axonal variety (acute motor axonal and acute sensory and motor axonal variants). Axonal variants are distinctly infrequent. Two brothers (18 years and 15 years) were hospitalized on the same day with complaints of acute symmetric upper- and lower-limb weakness of 7 days' duration. They did not have overt manifestations of dengue fever which preceded the neurological presentation...
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532364/paraneoplastic-cerebellar-degeneration-associated-with-ovarian-adenocarcinoma-a-case-report-and-review-of-literature
#14
Pushpendra Nath Renjen, Dinesh Mohan Chaudhari, U S Shilpi, Dhruv Zutshi, Kamal Ahmad
Paraneoplastic syndromes are a rare heterogeneous group of disorders that are indicators of the underlying occult malignancy. Subacute cerebellar ataxia in a patient with a known cancer is often due to metastatic invasion or other complications of the cancer, such as infection, coagulopathy, metabolic and nutritional deficits, or side effects of treatment. When tumor- and treatment-related causes have been excluded, the patient is considered to suffer from paraneoplastic cerebellar degeneration (PCD). We report a case of PCD that presented before any evidence of tumor, but early diagnostic workup and clinical vigilance helped us to find the underlying high-grade ovarian adenocarcinoma which was surgically removed later...
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532363/extensive-extrapulvinar-calcification-in-fabry-disease
#15
Jitupam Baishya, Praveen Kesav, Sheela Nampoothiri, Sapna Erat Sreedharan, P N Sylaja
No abstract text is available yet for this article.
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532362/giant-axonal-neuropathy-clinical-radiological-and-genetic-features
#16
Meenal Garg, Shilpa D Kulkarni, Anaita Udwadia Hegde, Margi Desai, Rafat J Sayed
Introduction: Giant axonal neuropathy (GAN) is an inherited neurodegenerative disorder caused by mutations in the GAN gene. It affects both the central and peripheral nervous systems. We discuss clinical, electrophysiological, radiological and genetic features in three new unrelated patients with GAN. Methods: Three pediatric patients with suspected GAN were included. The diagnosis was considered in patients with early onset polyneuropathy and characteristic hair with central nervous system involvement or suggestive neuroimaging findings...
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532361/cognitive-and-behavioral-profile-of-treatment-na%C3%A3-ve-children-aged-6-14-years-with-neurocysticercosis-from-north-india
#17
Anjali Verma, Bhavna Chopra, Jaya Shankar Kaushik, Geeta Gathwala
Background: Neurocysticercosis (NCC) produces a progressive organic brain damage by altering brain function with alterations in memory, difficulties in learning, and behavioral changes. The present study was designed to compare the cognitive and behavioral profile of school-going children aged 6-14 years with newly diagnosed NCC with their age-matched controls. Materials and Methods: A descriptive cross-sectional study was conducted among children aged 6-14 years with newly (<7 days) diagnosed NCC...
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532360/epidemiological-survey-of-neurological-diseases-in-a-tribal-population-cluster-in-gujarat
#18
Khushnuma A Mansukhani, Maria A Barretto, Sharmila A Donde, Jagruti Wandrekar, Advaita Nigudkar, Ridhi Nair
Background: There are few community-based neuroepidemiological studies based in tribal communities. This cross-sectional community-based study explored the prevalence rates of neurological disorders in the tribal region of Kaparada in Gujarat. Methodology: A two-stage methodology was used. Door-to-door surveys were conducted in the villages of Moti Vahiyal, Arnai, and Chavshala in Kaparada taluka in the Valsad district. Trained volunteers administered a questionnaire that assessed demographic details and common neurological symptoms in children and adults...
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532359/validation-of-marathi-version-of-stroke-specific-quality-of-life
#19
Suvarna Ganvir, Maheshwari Harishch, Chetana Kunde
Background and Purpose: One of the most important patient-centered outcomes in patients with stroke is quality of life. Apart from physical affection, stroke affects cognitive, emotional language along with social functioning. Stroke-specific quality of life (SSQOL) is a measure to assess the quality of life in patients with stroke. The aim of this study is to investigate the reliability and validity of Marathi version of SSQOL in patients with stroke. Methodology: Translation of SSQOL in Marathi language was performed in accordance with the published guidelines...
October 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/30532358/quality-of-communication-life-in-individuals-with-broca-s-aphasia-and-normal-individuals-a-comparative-study
#20
Jagadeesan Pallavi, Radhakrishnan Chella Perumal, Murugesan Krupa
Background: Aphasia is a neurogenic communication disorder with significant deficits in various domains of language and communication. One such type of aphasia, which impacts the quality of life significantly is Broca's aphasia, where the individual is aware of the communication difficulty. Objective: To compare the Quality of Communication Life (QoCL) between individuals with Broca's aphasia and normal individuals. Methods: The first phase of the study translated and validated QCL scale in Tamil...
October 2018: Annals of Indian Academy of Neurology
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