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Biomarkers of residual risk and all-cause mortality after acute coronary syndrome.
Published 2025-03-01Subjects: Get full text
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162
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163
Maternal erythrocytosis as a risk factor for small for gestational age at term in high altitude
Published 2025-02-01Subjects: Get full text
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164
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165
Cerebral tissue oxygen desaturations and increased fractional oxygen extraction events vary by gestational age in preterm infants
Published 2025-01-01Subjects: Get full text
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166
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The prognostic significance of malnutrition in older adult patients with acute ischemic stroke
Published 2025-01-01Subjects: Get full text
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168
Detection of Hemoglobinopathies in Cuban Pregnant Women from the Program: Sickle Cell Anemias in Cuba
Published 2024-01-01“…The research meth-od was hemoglobin electrophoresis in agarose gels at alkaline pH. …”
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169
Prevention of Cyclophosphamide-Induced Immunosuppression in Mice with the Antimicrobial Peptide Sublancin
Published 2018-01-01“…In cyclophosphamide-treated mice, oral sublancin administration accelerated the recovery of peripheral white blood cells, red blood cells, hemoglobins, and platelets and enhanced the macrophage phagocytic activity. …”
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170
Principles of Medical Biochemistry /
Published 2017Table of Contents: “…Introduction to biomolecules -- Introduction to protein structure -- Oxygen-binding proteins : hemoglobin and myoglobin -- Enzymatic reactions -- Coenzymes -- DNA, RNA, and protein synthesis -- The human genome -- Protein targeting and proteostasis -- Introduction to genetic diseases -- Viruses -- DNA technology -- Biological membranes -- The cytoskeleton -- The extracellular matrix -- Extracellular messengers -- Intracellular messengers -- Plasma proteins -- Defense mechanisms -- Cellular growth control and cancer -- Digestive enzymes -- Introduction to metabolic pathways -- Glycolysis, tricarboxylic acid cycle, and oxidative phosphorylation -- Oxygen deficiency and oxygen toxicity -- Carbohydrate metabolism -- The metabolism of fatty acids and triglycerides -- The metabolism of membrane lipids -- Lipid transport -- Amino acid metabolism -- Metabolism of iron and heme -- The metabolism of purines and pyrimidines -- Micronutrients -- Integration of metabolism.…”
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171
Clinical Chemistry : fundamentals and laboratory techniques /
Published 2017Table of Contents: “…Overview of clinical chemistry / Jean Brickell, Wendy Arenson, and Diana Mass -- Quality assessment / Margaret Crellin, Marian Cavagnaro, and Wendy Arneson -- Laboratory techniques and instrumentation / Wendy Arenson and Jean Brickell -- Diabetes and other carbohydrate disorders / Jean Brickell, Vicki Freeman, and Wendy Arneson -- Hemoglobin production disorders and testing / Vicki Freeman and Wendy Arneson -- Assessment of renal function / Wendy Arneson and Jean Brickell -- Assessment of liver function / Wendy Arneson and Jean Brickell -- Assessment of cardiovascular disorders / Linda S. …”
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172
Hemoprotein dalam Tubuh Manusia
Published 2012-07-01“…Struktur hem pada pigmen fotosintesis (klorofil) tumbuhan sama dengan hemoglobin pada manusia, tetapi ion logam pada klorofil adalah magnesium (Mg) sedangkan pada hemoglobin adalah besi (Fe). …”
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173
Elevated Circulating Angiogenic Progenitors and White Blood Cells Are Associated with Hypoxia-Inducible Angiogenic Growth Factors in Children with Sickle Cell Disease
Published 2012-01-01“…We studied the number and function of angiogenic progenitor cells and growth factors in children aged 5–18 years without acute illness, 43 with Hemoglobin SS and 68 with normal hemoglobin. Hemoglobin SS subjects had at least twice as many mononuclear cell colonies and more circulating progenitor cell than Control subjects. …”
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174
EF Bart’s Disease with Coinheritance of Gγ-XmnI and Aγ-Globin Polymorphisms: A Case of Nontransfusion-Dependant Thalassemia
Published 2020-01-01“…EF Bart’s disease is a rare form of nontransfusion-dependant thalassemia (NTDT) due to the coinheritance of homozygous hemoglobin E (βE/βE) genotype with hemoglobin H disease. …”
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175
Sickle Cell Anemia, the First Molecular Disease: Overview of Molecular Etiology, Pathophysiology, and Therapeutic Approaches
Published 2008-01-01“…The root cause of sickle cell disease is a single β-globin gene mutation coding for the sickle β-hemoglobin chain. Sickle hemoglobin tetramers polymerize when deoxygenated, damaging the sickle erythrocyte. …”
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176
Infusion of Autologous Retrodifferentiated Stem Cells into Patients with Beta-Thalassemia
Published 2006-01-01“…This was always accompanied by an increase in mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), and mean corpuscular hemoglobin concentration (MCHC) in such patients. …”
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177
One Year Obstetric Experience with Extreme Complications in a Tertiary Center in Somalia
Published 2022-12-01“…All maternal demographic data, prenatal hemoglobin levels, serological markers, and complications were recorded. …”
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178
Effects of a New Patient Safety-Driven Oxytocin Dosing Protocol on Postpartum Hemorrhage
Published 2014-01-01“…Retrospective cohort study comparing 8 months before to 8 months after the change. PP day 1 hemoglobin was subtracted from admission hemoglobin. …”
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179
Renal Anemia Control in Lithuania: Influence of Local Conditions and Local Guidelines
Published 2013-01-01“…Although hemoglobin variability was common in Lithuanian hemodialysis patients, we did not find the association between hemoglobin variability and all-cause mortality in our study.…”
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180
The effect of blood transfusion on serum hepcidin levels in chronically transfused patients of β-thalassemia major: An observational study in a tertiary care centre in Western Maha...
Published 2024-01-01“…RESULTS: Posttransfusion levels of hemoglobin, serum ferritin, and serum hepcidin increased. …”
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