Search Results - "Jaiswal, Preeti"

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  1. 1

    Guillain Barré Syndrome and its variants as a manifestation of COVID-19: A systematic review of case reports and case series by Sriwastava, Shitiz, Kataria, Saurabh, Tandon, Medha, Patel, Jenil, Patel, Riddhi, Jowkar, Abbas, Daimee, Maha, Bernitsas, Evanthia, Jaiswal, Preeti, Lisak, Robert P.

    Published in Journal of the neurological sciences (15-01-2021)
    “…The COVID-19 pandemic caused by SARS-COV-2 began in Wuhan, China in December 2019. Reports of COVID-19 with central (CNS) and peripheral nervous (PNS) system…”
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    Journal Article
  2. 2

    Association of Dopamine Transporter Gene with Heroin Dependence in an Indian Subpopulation from Manipur by Koijam, Arunkumar Singh, Hijam, Aruna Chanu, Singh, Asem Surindro, Jaiswal, Preeti, Mukhopadhyay, Kanchan, Rajamma, Usha, Haobam, Reena

    Published in Journal of molecular neuroscience (2021)
    “…Dopamine transporter (DAT) or solute carrier family 6 member 3 (SLC6A3) is a transmembrane protein regulating dopaminergic neurotransmission. It has been…”
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    Journal Article
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    Synthesis and Excited-State Properties of Donor–Acceptor Azahelical Coumarins by Jana, Kanyashree, Sarkar, Debarghya, Jaiswal, Preeti, Moorthy, Jarugu Narasimha

    Published in Journal of organic chemistry (02-06-2023)
    “…A set of three donor–acceptor azahelical coumarins (DA-AHCs), namely, H-AHC, Me-AHC, and Ph-AHC, were rationally designed and synthesized, and their…”
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    Journal Article
  5. 5

    Serotonin mediated immunoregulation and neural functions: Complicity in the aetiology of autism spectrum disorders by Jaiswal, Preeti, Mohanakumar, Kochupurackal P, Rajamma, Usha

    Published in Neuroscience and biobehavioral reviews (01-08-2015)
    “…Serotonergic system has long been implicated in the aetiology of autism spectrum disorders (ASD), since platelet hyperserotonemia is consistently observed in a…”
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    Genetic defects in Indian Wilson disease patients and genotype–phenotype correlation by Mukherjee, Shashwata, Dutta, Shruti, Majumdar, Sulagna, Biswas, Tamoghna, Jaiswal, Preeti, Sengupta, Mainak, Bhattacharya, Abhisek, Gangopadhyay, Prasanta K, Bavdekar, Ashish, Das, Shyamal K, Ray, Kunal

    Published in Parkinsonism & related disorders (01-01-2014)
    “…Abstract Wilson disease (WD) is caused by defects in ATP7B gene due to impairment of normal function of the copper transporting P-type ATPase. This study…”
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    Journal Article