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     <title><![CDATA[NUST Institutions Library Catalogue Search for 'kw,wrdl: (su-br:&quot;Synchronization.&quot;)']]></title>
     <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?idx=kw&amp;q=%28su-br%3A%22Synchronization.%22%29&amp;format=rss</link>
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     <description><![CDATA[ Search results for 'kw,wrdl: (su-br:&quot;Synchronization.&quot;)' at NUST Institutions Library Catalogue]]></description>
     <opensearch:totalResults>7</opensearch:totalResults>
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     <item>
       <title>
    Advances in 3G enhanced technologies for wireless communications 






</title>
       <dc:identifier>ISBN:1580533027</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=8391</link>
        
       <description><![CDATA[









	   <p>
	   Boston, MA : Artech House, 2002
                        . xv, 350 p. :
                        , Based on selected papers from the Fourth IEEE Workshop on Emerging Technologies in Circuits and Systems--Third Generation (3G) Mobile Technologies and Applications, held Nov. 29-Dec. 1, 2000, in Hong Kong.
                         24 cm.. 
                         1580533027
       </p>

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						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=8391</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
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     <item>
       <title>
    Software simulation of discrete multitone modem /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=182753</link>
        
       <description><![CDATA[









	   <p>By Khan , NC Hassan Talha  (TCC-11). 
	   Rawalpindi MCS (NUST) 2003
                        . 144  p.;
                        
                        
                        
       </p>

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						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=182753</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
     <opensearch:Query role="request" searchTerms="" startPage="" />
     <item>
       <title>
    Recent Advances in Biomedical Engineering (E-Book)






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=192329</link>
        
       <description><![CDATA[









	   <p>By Dr Ganesh R Naik. 
	   India In-Teh 2009
                        . xii,660 P;
                        
                        
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=192329">Place Hold on <em>Recent Advances in Biomedical Engineering (E-Book)</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=192329</guid>
     </item>
	 
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     <item>
       <title>
    Mathematical Control Theory  :


    An Interoduction/





</title>
       <dc:identifier>ISBN:9780817647322</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=593988</link>
        
       <description><![CDATA[









	   <p>
	   
                        . 260p.
                        
                        
                         9780817647322
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=593988">Place Hold on <em>Mathematical Control Theory  :</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=593988</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
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     <item>
       <title>
    Identifying Neurophysiological Correlates of Frontotemporal Dementia: Resting State EEG and Phase Synchronization Analysis /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=610274</link>
        
       <description><![CDATA[









	   <p>By Ali, Salwa . 
	   
                        . 123p.
                        , The need to develop more efficient neuropsychological biomarkers is paramount in the
identification of neurodegenerative diseases, tracking the efficiency of treatment and in an
effort to avoid the huge financial cost required. While previous research utilizing
neuroimaging techniques has pinpointed changes in functional connectivity (FC) as
promising biomarkers for frontotemporal dementia (FTD), the constraints of cost and
availability of neuroimaging equipment underscore the necessity for accessible
alternatives. Electroencephalography (EEG) has emerged as a viable option due to its
increasing robustness, wider usage, and affordability.
To this end, the research focuses on a resting-state EEG data created from AD, FTD, and
HC groups. Here ground data were obtained from nineteen leads using a clinical EEG
device when the subjects were in a resting state and their eyes were closed. Another
challenge was to follow strict standards for data quality and quality management for data
quality to enhance consistency. It is a cross-sectional study, including data from MiniMental State Examination conducted on each participant, and tapes recorded from 20 AD
patients, 20 FTD patients, and 20 HC. The Neuroimaging Data Structure (BIDS) format
was utilized to present both preprocessed and raw EEG data.
The foremost aim was to determine the Feasibility, Sensitivity, and Specificity of the
preprocessed, feature extracted, time-efficient, and artifact reduced EEG-derived FC
patterns as markers in FTD. Phase-lock values (PLVs) were computed among nineteen
pairs of electrodes across five frequency bands using MATLAB and the Hilbert transform.
Significant variations in brain connectivity were identified through statistical analyses.
The study revealed significant differences in alpha and beta frequency patterns among the
control, Alzheimer's, and FTD groups, particularly in frontal and temporal regions. These
differences suggest alterations in neural activity associated with cognitive processing,
potentially serving as biomarkers for distinguishing between the three groups.
Alterations in beta frequency PLV were noted across various EEG pairs, indicating
disruptions in neural communication and coordination. These alterations suggest
xvi
compensatory mechanisms or hyperactivity in frontal and prefrontal regions, alongside
potential cognitive and motor deficits due to decreased PLV in central and temporal
regions.
While no statistically significant differences were observed in delta and theta frequency
synchronization between groups, trends suggest potential regions of interest for further
research, aligning with existing literature exploring neural oscillations in
neurodegenerative diseases. Similarly, no significant differences were observed in gamma
frequency synchronization between groups, indicating relatively preserved neural
synchronization in this frequency range across control, Alzheimer's, and FTD patients.
In summary, both Alzheimer's and FTD demonstrate significant reductions in alpha and
beta frequency values, particularly in frontal and temporal regions, compared to healthy
controls. These findings underscore the altered functional network topology in AD and
FTD, offering valuable insights into the neural mechanisms underlying these conditions.
The study's results contribute to the development of electrophysiological markers,
potentially enhancing the clinical diagnosis and understanding of AD and FTD. The
specificity and sensitivity of EEG-derived FC patterns highlight their potential as costeffective, accessible biomarkers for neurodegenerative disease.
                         30cm. 
                        
       </p>

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						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=610274</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
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     <item>
       <title>
    Therapeutic Potential of Light Flicker for Schizophrenia - A Comparative Study






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=613798</link>
        
       <description><![CDATA[









	   <p>By  Ihsan ,Faryal. 
	   
                        . 93p. ;
                        , Schizophrenia is a serious neuropsychiatric condition that affects cognition, perception, and
behavior. Current pharmacological treatments are successful in treating symptoms but can have
serious adverse effects, especially in susceptible populations such as children and the elderly.
These negative consequences, which range from metabolic problems to cognitive impairment,
underline the critical need for alternate, non-invasive therapeutic techniques. One promising
approach is neuromodulation by gamma entrainment with sensory stimulation, which uses an
external stimulus to restore broken neuronal synchronization. This study looks at the combined
effects of Clozapine and light flicker therapy in a ketamine-induced schizophrenia mouse model,
with the hypothesis that their synergistic action will lead to improved recovery. Mice were
classified into five groups: control, diseased, Clozapine-treated, light flicker-treated, and
combination therapy. Behavioral examinations, such as the open field test, elevated plus maze,
forced swim test, tail suspension test, novel object recognition, and Y-maze, demonstrated that
combination therapy improved cognitive and affective deficiencies the most significantly.
Histological analysis with hematoxylin and eosin staining of the cortex and hippocampus (CA1
and CA3) revealed severe neuronal disorganization in the diseased group, partial restoration in
the individual treatment groups, and near-control level preservation in the combination therapy
group. RT-PCR analysis using Pvalb and BDNF primers indicated abnormalities in PV
interneurons and neuroplasticity markers, which corroborated the histological and behavioral
findings. Our approach to schizophrenia combines neuroscience and psychology. Restoring
gamma oscillations with light flicker improves PV interneuron function, BDNF production, and
cognitive stability. This neuronal synchronization minimizes ego fragmentation, improves self perception, and promotes cognitive integration for a more comprehensive treatment.
                         30cm.. 
                        
       </p>

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						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=613798</guid>
     </item>
	 
     <atom:link rel="search" type="application/opensearchdescription+xml" href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-search.pl?&amp;sort_by=&amp;format=opensearchdescription"/>
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     <item>
       <title>
    Therapeutic Effects of Sound-Mediated Stimulation in a Mouse Model of Depression - A Comparative Study /






</title>
       <dc:identifier>ISBN:</dc:identifier>
        
        <link>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=615203</link>
        
       <description><![CDATA[









	   <p>By Reemaz, Tooba . 
	   
                        . 90p.
                        , Depression is a prevalent neuropsychiatric disorder characterized by mood disturbances, cognitive
impairment, and behavioral deficits. While pharmacological treatments such as Fluoxetine are
widely used, they often represent limitations including delayed onset of action and side effects,
highlighting the need for alternative, non-invasive therapeutic strategies. One promising approach
is neuromodulation through gamma entrainment using auditory stimulation, aimed at restoring
disrupted neuronal synchronization. This study evaluates the effects of 40 Hz sound stimulation
compared to fluoxetine in a chronic restraint stress-induced mouse model of depression,
hypothesizing that sound therapy will yield superior recovery outcomes. Mice were divided into
control, depressed, fluoxetine-treated, and sound stimulation-treated groups. Behavioral
assessments, including the Tail Suspension Test, Forced Swim Test, Social Interaction Test,
Sucrose Preference Test, Open Field Test, and Light-Dark Box Test, revealed that 40 Hz sound
therapy significantly alleviated depressive-like behaviors, often outperforming fluoxetine.
Histopathological analysis focused on the hippocampus and prefrontal cortex showed that sound
stimulation preventing neuronal loss and parvalbumin-expressing interneurons, which are crucial
for inhibitory circuit function and gamma oscillatory activity. Molecular evaluation through qPCR
for pavlb and brain-derived neurotrophic factor; BDNF supported these findings, displaying
increased expression levels indicating enhanced interneuron integrity and neuroplasticity. This
neuromodulatory treatment encourages the molecular and functional repair of brain circuitry
implicated in depression. The findings demonstrated 40 Hz sound entrainment's ability to change
brain oscillations and ameliorate cellular and behavioral deficiencies linked to depression,
indicating that it may be a novel supplement or substitute for traditional antidepressant treatments.
                         30cm. 
                        
       </p>

<p><a href="http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-reserve.pl?biblionumber=615203">Place Hold on <em>Therapeutic Effects of Sound-Mediated Stimulation in a Mouse Model of Depression - A Comparative Study /</em></a></p>

						]]></description>
       <guid>http://catalogue.nust.edu.pk:8081/cgi-bin/koha/opac-detail.pl?biblionumber=615203</guid>
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