Search Results - "Banerjee, Tapas K"
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Evaluation of PARKIN gene variants in West Bengal Parkinson's disease patients
Published in Journal of human genetics (01-09-2015)“…Little information is available regarding the molecular pathogenesis of Parkinson's disease (PD) among the Bengalee population in West Bengal, India. This…”
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Community survey of primary dystonia in the city of Kolkata, India
Published in Movement disorders (31-10-2007)“…An epidemiological study on dystonia has not been reported from India. As part of a major study to find out the prevalence of major neurological disorders in…”
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3
Identification of GBA mutations among neurodegenerative disease patients from eastern India
Published in Neuroscience letters (23-04-2021)“…•Screening of selected Parkinsonism associated GBA mutations was done among Neurodegenerative disease patients from eastern India.•GBA mutations are more…”
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4
Classical imaging findings in spinal subdural hematoma - "Mercedes-Benz" and "Cap" signs
Published in British journal of neurosurgery (02-01-2016)Get full text
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5
A prospective community-based study of stroke in Kolkata, India
Published in Stroke (1970) (01-03-2007)“…Information on essential stroke parameters are lacking in India. This population-based study on stroke disorder was undertaken in the city of Kolkata, India,…”
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Role of LRRK2 variant p.Gly2019Ser in patients with Parkinsonism
Published in Indian journal of medical research (New Delhi, India : 1994) (01-06-2020)“…Background & objectives: Parkinsonian disorder, including Parkinson's disease (PD), is an aetiologically complex neurodegenerative disorder. Mutations in…”
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7
Indian Consensus on the Role of Amitriptyline in Migraine Prophylaxis
Published in Curēus (Palo Alto, CA) (15-02-2024)“…Migraine is a globally prevalent neurological disorder. Amitriptyline, a tricyclic antidepressant, has shown potential as a prophylactic treatment for…”
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Prevalence, burden, and risk factors of migraine: A community-based study from Eastern India
Published in Neurology India (01-11-2017)“…Headache is common in communities; however, epidemiological research regarding its prevalence is infrequent in India. We planned to study the prevalence of…”
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Neurological disorders in children and adolescents
Published in Indian journal of pediatrics (01-02-2009)“…Objective To ascertain the prevalence of active epilepsy, febrile seizures (FS), cerebral palsy (CP) and tic disorders (TD) in aged 19 years or less. Methods…”
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Physiological characterization of neuropathy in Fabry's disease
Published in Muscle & nerve (01-11-2002)“…Fabry's disease is commonly associated with a painful, debilitating neuropathy. Characterization of the physiological abnormalities is an important step in…”
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Analysis of hospital-based stroke registry in a neurological centre in Kolkata
Published in Journal of the Indian Medical Association (01-12-2005)“…This was a retrospective analysis of 7-year (January 1995-December 2001) hospital-based in-patient medical records of stroke cases (subarachnoid haemorrhage…”
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12
Analysis of dystrophin gene deletions by multiplex PCR in eastern India
Published in Neurology India (01-07-2006)“…The most common genetic neuromuscular disease of childhood, Duchenne and Becker muscular dystrophy (DMD/BMD) is caused by deletion, duplication or point…”
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The burden of neurological disorders across the states of India: the Global Burden of Disease Study 1990–2019
Published in The Lancet global health (01-08-2021)“…A systematic understanding of the burden of neurological disorders at the subnational level is not readily available for India. We present a comprehensive…”
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14
Classical imaging findings in spinal subdural hematoma - "Mercedes-Benz" and "Cap" signs
Published in British journal of neurosurgery (09-08-2015)Get full text
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15
Severe Hyponatremia with Hypouricemia in a Patient with Medullary Hemorrhage: A Case Report
Published in EJIFCC (04-04-2012)“…Hyponatremia is the commonest electrolyte abnormality in hospitalized patients and occurs due to various causes. Here we present a case of SIADH who was…”
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Enzyme therapy in type 1 Gaucher disease : comparative efficacy of mannose-terminated glucocerebrosidase from natural and recombinant sources
Published in Annals of internal medicine (1995)“…To compare the efficacy of mannose-terminated glucocerbrosidase prepared from natural (alglucerase; Ceredase, Genzyme Corp., Cambridge, Massachusetts) and…”
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Oligomerization of Vibrio cholerae Hemolysin Induces CXCR3 Upregulation and Activation of B-1a Cell
Published in Cellular & molecular immunology (01-06-2008)“…The hemolysin oligomer promotes the proliferation of B-1a cells and the expression of CD25, which is indicative of cell activation, on B-1a cells. The…”
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Prospective study of neurological responses to treatment with macrophage-targeted glucocerebrosidase in patients with type 3 Gaucher's disease
Published in Annals of neurology (01-10-1997)“…We prospectively evaluated the clinical and biochemical responses to enzyme-replacement therapy (ERT) with macrophage-targeted glucocerebrosidase (Ceredase)…”
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Brief Report - Analysis of dystrophin gene deletions by multiplex PCR in eastern India
Published in Neurology India (20-06-2006)“…The most common genetic neuromuscular disease of childhood, Duchenne and Becker muscular dystrophy (DMD/BMD) is caused by deletion, duplication or point…”
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20
Severe Hyponatremia with Hypouricemia in a Patient with Medullary Hemorrhage: A Case Report
Published in EJIFCC (01-04-2012)Get full text
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