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Familial Hypercholesterolemia: Genetics, Symptoms, Diagnosis and Treatment - A Literature Overview
Published 2025-02-01Get full text
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Identification of Interactive Genetic Loci Linked to Insulin Resistance in Metabolic Syndrome—An Update
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Non-Invasive Cancer Detection Using Blood Test and Predictive Modeling Approach
Published 2025-01-01“…The HGB model showed improved performance on the dataset.Conclusion: After investigating a number of machine learning methods, an efficient screening platform for non-invasive cancer detection is provided by the integration of haematological indicators with proper analytical data. …”
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Hereditary Xerocytosis due to Mutations in PIEZO1 Gene Associated with Heterozygous Pyruvate Kinase Deficiency and Beta-Thalassemia Trait in Two Unrelated Families
Published 2017-01-01“…We report the clinical, haematological, and molecular characteristics of four patients from two unrelated Italian families affected by HX, associated with beta-thalassemia trait and heterozygous pyruvate kinase deficiency, respectively. …”
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Ocular Signs and Ocular Comorbidities in Monoclonal Gammopathy: Analysis of 80 Subjects
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Burden of Antimicrobial Resistance in Adult Hospitalized Patients With Cancer: A Multicenter Analysis
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Protocol for faecal microbiota transplantation in irritable bowel syndrome: the MISCEAT study – a randomised, double-blind cross-over study using mixed microbiota from healthy dono...
Published 2022-06-01“…Food records, dietary questionnaires, anthropometry, bioimpedance, biochemistry and haematology workup will be obtained at study visits during the follow-up period. …”
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Impaired Fibrinolysis in Angiographically Documented Coronary Artery Disease
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Paediatric nephroblastoma at a South African tertiary hospital: A 21-year retrospective analysis
Published 2024-11-01“…This retrospective cross-sectional study included 207 paediatric oncology patients treated for nephroblastoma at the Paediatric Haematology and Oncology Unit at UAHC, Bloemfontein, SA, from January 2000 to December 2020. …”
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Subclinical Inflammatory Status in Rett Syndrome
Published 2014-01-01“…., “pseudo-autistic”) RTT patients by routine haematology/clinical chemistry and proteomic 2-DE/MALDI-TOF analyses as a function of four major MECP2 gene mutation types (R306C, T158M, R168X, and large deletions). …”
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Thromboelastometry-Based Profiling of Haemostatic Alterations in Neonatal Sepsis by Causative Pathogens
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