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    <title>DSpace Collection: 1-54</title>
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    <dc:date>2026-04-08T23:00:33Z</dc:date>
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  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/11846">
    <title>Navigating the 2024 revised guidelines for Undergraduate Competency Based Medical Education (CBME) curriculum: Newer insights and implications for biochemistry education</title>
    <link>http://localhost:8080/xmlui/handle/123456789/11846</link>
    <description>Title: Navigating the 2024 revised guidelines for Undergraduate Competency Based Medical Education (CBME) curriculum: Newer insights and implications for biochemistry education
Authors: Mohan Surapaneni, Krishna
Abstract: The recent release of the 2024 revised guidelines for the Competency Based Medical Education (CBME) curriculum&#xD;
by the National Medical Commission (NMC) marks a pivotal moment in the evolution of medical education in India.&#xD;
Building upon the foundation established in 2019, this revised curriculum introduces critical advancements designed&#xD;
to align medical training with contemporary global standards. These updates not only enhance the educational experience&#xD;
but also ensure that future medical professionals are equipped with the knowledge, skills, and competencies necessary&#xD;
to thrive in modern healthcare environments. This article focuses on the significant changes within the biochemistry&#xD;
curriculum, highlighting its importance and the shift towards integrating clinical relevance, innovative teaching&#xD;
methodologies, and robust assessment strategies. Educators are encouraged to prioritize tailoring their teaching approaches&#xD;
according to these expected standards. The article also provides strategies for incorporating these changes&#xD;
into teaching methodologies, offering educators evidence-informed guidance.&#xD;
Keywords: Assessment strategies, biochemistry curriculum, clinical relevance, Competency Based Medical Education&#xD;
(CBME), teaching methods</description>
    <dc:date>2025-01-01T00:00:00Z</dc:date>
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  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/11845">
    <title>Investigation of a number of rare deletional mutations in the alpha globin gene cluster</title>
    <link>http://localhost:8080/xmlui/handle/123456789/11845</link>
    <description>Title: Investigation of a number of rare deletional mutations in the alpha globin gene cluster
Authors: Arash, Majid
Abstract: Alpha thalassemia is one of the most common genetic diseases in the world. This disease is prevalent in various parts&#xD;
of the world, such as India, the Middle East, Africa, and many other countries. Several clinical conditions can result&#xD;
from mutations. In the condition where only one of the alpha globin genes is expressed, hemoglobin H disease (Hb H)&#xD;
occurs. Alpha thalassemia trait and silent carrier are milder forms of the disease, caused by the deletion of one and two&#xD;
alpha globin genes, respectively. Several mutations result in the deletion of alpha-globin. Seven common deletional&#xD;
mutations include -α4.2, -α3.7, -(α)20.5, --MED, --SEA, --Fil, and --THAI. The deletional mutations -α4.2 and -α3.7 remove only one of&#xD;
the alpha globin genes, while others remove both α1 and α2 globin genes from the gene cluster. Nowadays, laboratories&#xD;
identify these mutations using the Gap PCR method and other advanced methods. In addition to these mutations,&#xD;
some deletional mutations are found only in certain families or certain regions.&#xD;
Keywords: Alpha thalassemia, deletional mutation, globin, hydrops fetalis</description>
    <dc:date>2025-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/11844">
    <title>Evaluation of the hemolysis threshold for the measurement of serum lipase on Roche Cobas systems</title>
    <link>http://localhost:8080/xmlui/handle/123456789/11844</link>
    <description>Title: Evaluation of the hemolysis threshold for the measurement of serum lipase on Roche Cobas systems
Authors: Ilardo, Claudio; Al Muhanna, Batricia
Abstract: Objectives: Following the release of an informational bulletin, Roche Diagnostics adopted a more restrictive hemolysis&#xD;
index (100 HI) for the release of serum lipase results on all Cobas systems. This study aimed to evaluate the interference&#xD;
threshold for serum lipase hemolysis on Cobas C501/311/701/Integra 400 systems using a total allowable error set by&#xD;
the Royal College of Pathologists of Australasia (RCPA).&#xD;
Methods: To assess the influence of hemolysis on lipase, the parameter was quantified in serum pools spiked with&#xD;
escalating concentrations of a hemolysis interferent. The lipase assay was performed using the colorimetric lipase&#xD;
method (LIPC), and the HI was determined by absorbance measurements of diluted samples in accordance with the&#xD;
system protocol.&#xD;
Results: The Cobas Integra 400 and Cobas C311 showed the greatest interference of lipase with hemolysis (≤300 HI).&#xD;
The Cobas C501 and C701 demonstrated less sensitivity to hemolysis (≤1300 HI).&#xD;
Conclusion: The results of this study demonstrate that interference limits may vary between different Roche systems,&#xD;
even when the same reagent is used. Our study indicated that the lipase hemolysis threshold (100 HI) currently set by&#xD;
the manufacturer was excessively restrictive. This finding highlights the necessity of verifying manufacturers' information&#xD;
bulletins to provide better medical care.&#xD;
Keywords: Hemolysis, interference, lipase, threshold</description>
    <dc:date>2025-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/11843">
    <title>Diagnostic accuracy of the combination of fecal calprotectin and occult blood tests in inflammatory bowel disease</title>
    <link>http://localhost:8080/xmlui/handle/123456789/11843</link>
    <description>Title: Diagnostic accuracy of the combination of fecal calprotectin and occult blood tests in inflammatory bowel disease
Authors: Unal, Kubranur; Karatas, Ali; Gulbahar, Ozlem; Ozbas, Cansu
Abstract: Objectives: This study aimed to assess the diagnostic accuracy of the fecal occult blood test (FOBT), fecal calprotectin&#xD;
(FC), and the combination of these markers in patients with suspected inflammatory bowel disease (IBD). Additionally,&#xD;
FC levels were compared between patients monitored for IBD and those newly diagnosed with IBD.&#xD;
Methods: Conducted at Gazi University Application and Research Hospital, this retrospective study reviewed demographic,&#xD;
clinical, colonoscopy reports, and laboratory data (FC and FOBT) of IBD patients. The final analysis included 153&#xD;
patients with suspected IBD to evaluate the diagnostic accuracy of FOBT, FC, and their combination. FC was analyzed&#xD;
using the Quantum Blue® fCAL extended test. The ROC curve was drawn to determine the diagnostic ability of FC, and the&#xD;
area under the curve (AUC) was calculated. Sensitivity, specificity, and predictive values were determined for FC and FOBT.&#xD;
Results: The AUC was determined as 0.827 (95% CI:0.742–0.913) for FC (p&lt;0.001). FC showed a sensitivity of 85.7%,&#xD;
specificity of 62.4%, positive predictive value (PPV) of 30.6%, and negative predictive value (NPV) of 95.8%. FOBT had a&#xD;
sensitivity of 81.3%, specificity of 78.1%, PPV of 30.2%, and NPV of 97.3%. The combination of FOBT and FC, with positivity&#xD;
in at least one of the tests, had a sensitivity of 93.8%, specificity of 63.5%, PPV of 23.1%, and NPV of 98.9%. The&#xD;
combined use of FOBT and FC demonstrated higher diagnostic accuracy than either test alone.&#xD;
Conclusion: The combination of FOBT and FC provides superior diagnostic accuracy for identifying suspected IBD&#xD;
patients compared to each test alone. This combined approach could serve as a cost-effective strategy to avoid unnecessary&#xD;
invasive procedures.&#xD;
Keywords: Diagnostic accuracy, fecal calprotectin, fecal occult blood test, inflammatory bowel diseases</description>
    <dc:date>2025-01-01T00:00:00Z</dc:date>
  </item>
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