Search Results - "Banerjee, Tapas K"

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  1. 1

    Evaluation of PARKIN gene variants in West Bengal Parkinson's disease patients by Sanyal, Jaya, Jana, Arpita, Ghosh, Epsita, Banerjee, Tapas K, Chakraborty, Durga P, Rao, Vadlamudi R

    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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    Journal Article
  2. 2

    Community survey of primary dystonia in the city of Kolkata, India by Das, Shyamal K., Banerjee, Tapas K., Biswas, Atanu, Roy, Trishit, Raut, Deepak K., Chaudhuri, Arijit, Hazra, Abhijit

    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. 3

    Identification of GBA mutations among neurodegenerative disease patients from eastern India by Biswas, Arindam, Sadhukhan, Dipanwita, Biswas, Atanu, Das, Shyamal K., Banerjee, Tapas K, Bal, Partha Sarathi, Pal, Sandip, Ghosh, Amitabha, Ray, Kunal, Ray, Jharna

    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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    A prospective community-based study of stroke in Kolkata, India by DAS, Shyamal K, BANERJEE, Tapas K, BISWAS, Atanu, ROY, Trishit, RAUT, Deepak K, MUKHERJEE, Chandra S, CHAUDHURI, Arijit, HAZRA, Avijit, ROY, Jayanta

    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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  6. 6

    Role of LRRK2 variant p.Gly2019Ser in patients with Parkinsonism by Sadhukhan, Dipanwita, Biswas, Arindam, Bhaduri, Arunima, Sarkar, Neelanjana, Biswas, Atanu, Das, Shyamal, Banerjee, Tapas, Ray, Kunal, Ray, Jharna

    “…Background & objectives: Parkinsonian disorder, including Parkinson's disease (PD), is an aetiologically complex neurodegenerative disorder. Mutations in…”
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  7. 7

    Indian Consensus on the Role of Amitriptyline in Migraine Prophylaxis by Singh, Sumit, Srinivasan, A V, Banerjee, Tapas K, Patel, Kanharam N, Muchhala, Snehal S, Kotak, Bhavesh P

    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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  8. 8

    Prevalence, burden, and risk factors of migraine: A community-based study from Eastern India by Ray, Biman K, Paul, Neelanjana, Hazra, Avijit, Das, Sujata, Ghosal, Malay K, Misra, Amar K, Banerjee, Tapas K, Chaudhuri, Arijit, Das, Shyamal K

    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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  9. 9

    Neurological disorders in children and adolescents by Banerjee, Tapas K., Hazra, Avijit, Biswas, Atanu, Ray, Jayanta, Roy, Trishit, Raut, Deepak K., Chaudhuri, Arijit, Das, Shyamal K.

    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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  10. 10

    Physiological characterization of neuropathy in Fabry's disease by Luciano, Carlos A., Russell, James W., Banerjee, Tapas K., Quirk, Jane M., Scott, Leland J.C., Dambrosia, James M., Barton, Norman W., Schiffmann, Raphael

    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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  11. 11

    Analysis of hospital-based stroke registry in a neurological centre in Kolkata by Banerjee, Tapas K, Choudhury, Debashis, Das, Ashis, Sekhar, Alakendu, Roy, Deepa, Sen, Suman

    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. 12

    Analysis of dystrophin gene deletions by multiplex PCR in eastern India by Basak, Jayasri, Dasgupta, Uma B, Banerjee, Tapas K, Senapati, Asit K, Das, Shyamal K, Mukherjee, Subhash C

    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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  13. 13

    The burden of neurological disorders across the states of India: the Global Burden of Disease Study 1990–2019 by Singh, Gagandeep, Sharma, Meenakshi, Kumar, G Anil, Rao, N Girish, Prasad, Kameshwar, Mathur, Prashant, Pandian, Jeyaraj D, Steinmetz, Jaimie D, Biswas, Atanu, Pal, Pramod K, Prakash, Sanjay, Sylaja, P N, Nichols, Emma, Dua, Tarun, Kaur, Harkiran, Alladi, Suvarna, Agarwal, Vivek, Aggarwal, Sumit, Ambekar, Atul, Bagepally, Bhavani S, Banerjee, Tapas K, Bender, Rose G, Bhagwat, Sadhana, Bhargava, Stuti, Bhatia, Rohit, Chakma, Joy K, Chowdhary, Neerja, Dey, Subhojit, Dirac, M Ashworth, Feigin, Valery L, Ganguli, Atreyi, Golechha, Mahaveer J, Gourie-Devi, M, Goyal, Vinay, Gupta, Gaurav, Gupta, Prakash C, Gupta, Rajeev, Gururaj, Gopalkrishna, Hemalatha, Rajkumar, Jeemon, Panniyammakal, Johnson, Catherine O, Joshi, Pradeep, Kant, Rajni, Kataki, Amal C, Khurana, Dheeraj, Krishnankutty, Rinu P, Kyu, Hmwe H, Lim, Stephen S, Lodha, Rakesh, Ma, Rui, Malhotra, Rajesh, Malhotra, Ridhima, Mathai, Matthews, Mehrotra, Ravi, Misra, Usha K, Mutreja, Parul, Naghavi, Mohsen, Naik, Nitish, Nguyen, Minh, Pandey, Anamika, Parmar, Priya, Perianayagam, Arokiasamy, Prabhakaran, Dorairaj, Rath, Goura K, Reinig, Nickolas, Roth, Gregory A, Sagar, Rajesh, Sankar, Mari J, Shaji, K S, Sharma, R S, Sharma, Shweta, Singh, Ravinder, Srivastava, M V Padma, Stark, Benjamin A, Tandon, Nikhil, Thakur, J S, ThekkePurakkal, Akhil S, Thomas, Sanjeev V, Tripathi, Manjari, Vongpradith, Avina, Wunrow, Han Y, Xavier, Denis, Shukla, D K, Reddy, K Srinath, Panda, Samiran, Dandona, Rakhi, Murray, Christopher J L, Vos, Theo, Dhaliwal, R S, Dandona, Lalit

    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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    Severe Hyponatremia with Hypouricemia in a Patient with Medullary Hemorrhage: A Case Report by Chakraborty, Sutirtha, Banerjee, Tapas K

    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 by GRABOWSKI, G. A, BARTON, N. W, PASTORES, G, DAMBROSIA, J. M, BANERJEE, T. K, MCKEE, M. A, PARKER, C, SCHIFFMANN, R, HILL, S. C, BRADY, R. O

    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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  17. 17

    Oligomerization of Vibrio cholerae Hemolysin Induces CXCR3 Upregulation and Activation of B-1a Cell by Mukherjee, Gayatri, Banerjee, Kalyan K, Biswas, Tapas

    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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  18. 18

    Prospective study of neurological responses to treatment with macrophage-targeted glucocerebrosidase in patients with type 3 Gaucher's disease by Schiffmann, R, Heyes, M P, Aerts, J M, Dambrosia, J M, Patterson, M C, DeGraba, T, Parker, C C, Zirzow, G C, Oliver, K, Tedeschi, G, Brady, R O, Barton, N W

    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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  19. 19

    Brief Report - Analysis of dystrophin gene deletions by multiplex PCR in eastern India by Basak Jayasri, Dasgupta Uma B, Banerjee Tapas K, Senapati Asit K, Das Shyamal K, Mukherjee Subhash C

    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…”
    Get full text
    Journal Article
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