Opin vísindi
→
Browsing by Subject

Browsing by Subject "Clinical Biochemistry"

Now showing items 1-7 of 7

Copeptin is associated with mortality in elderly people

Smaradottir, Maria Isabel; Andersen, Karl; Gudnason, Vilmundur; Näsman, Per; Rydén, Lars; Mellbin, Linda Garcia (2021-07)

BACKGROUND: Elevated copeptin, a marker for vasopressin release, has been associated with impaired prognosis in acute myocardial infarction (MI). The aim was to investigate whether this association extends beyond the acute phase and whether it is related ...
The effect of sample age on the metabolic information extracted from formalin-fixed and paraffin embedded tissue samples using desorption electrospray ionization mass spectrometry imaging

Ísberg, Ólöf Gerður; Xiang, Yuchen; Böðvarsdóttir, Sigríður Klara; Jónasson, Jón Gunnlaugur; Þorsteinsdóttir, Margrét; Takats, Zoltan (2021-11)

Background: Metabolites, especially lipids, have been shown to be promising therapeutic targets. In conjugation with genes and proteins they can be used to identify phenotypes of disease and support the development of targeted treatments. The majority ...
Fusion transcript analysis reveals slower response kinetics than multiparameter flow cytometry in childhood acute myeloid leukaemia

Karlsson, Lene; Nyvold, Charlotte Guldborg; Soboli, Anastasia; Johansson, Pegah; Palmqvist, Lars; Tierens, Anne; Hasle, Henrik; Lausen, Birgitte; Jónsson, Ólafur Gísli; Jürgensen, Gitte Wulff; Ebbesen, Lene Hyldahl; Abrahamsson, Jonas; Fogelstrand, Linda (2022-12)

Introduction: Analysis of measurable residual disease (MRD) is increasingly being implemented in the clinical care of children and adults with acute myeloid leukaemia (AML). However, MRD methodologies differ and discordances in results lead to difficulties ...
Improving prosthetic selection and predicting BMD from biometric measurements in patients receiving total hip arthroplasty

Ricciardi, Carlo; Jónsson, Halldór; Jacob, Deborah; Improta, Giovanni; Recenti, Marco; Gíslason, Magnús Kjartan; Cesarelli, Giuseppe; Esposito, Luca; Minutolo, Vincenzo; Bifulco, Paolo; Gargiulo, Paolo (2020-10-14)

There are two surgical approaches to performing total hip arthroplasty (THA): a cemented or uncemented type of prosthesis. The choice is usually based on the experience of the orthopaedic surgeon and on parameters such as the age and gender of the ...
Multifocal Neuroblastoma and Central Hypoventilation in An Infant with Germline ALK F1174I Mutation

Djos, Anna; Treis, Diana; Fransson, Susanne; Murkes, Lena Gordon; Wessman, Sandra; Ásmundsson, Jurate; Markstrom, Agneta; Kogner, Per; Martinsson, Tommy (2022-09-19)

A preterm infant with central hypoventilation was diagnosed with multifocal neuroblastoma. Congenital anomalies of the autonomic nervous system in association with neuroblastoma are commonly associated with germline mutations in PHOX2B. Further, the ...
Nicotinamide provides neuroprotection in glaucoma by protecting against mitochondrial and metabolic dysfunction

Tribble, James R.; Otmani, Amin; Sun, Shanshan; Ellis, Sevannah A.; Cimaglia, Gloria; Vohra, Rupali; Jöe, Melissa; Lardner, Emma; Venkataraman, Abinaya P.; Domínguez-Vicent, Alberto; Kokkali, Eirini; Rho, Seungsoo; Jóhannesson, Gauti; Burgess, Robert W.; Fuerst, Peter G.; Brautaset, Rune; Kolko, Miriam; Morgan, James E.; Crowston, Jonathan G.; Votruba, Marcela; Williams, Pete A. (2021-07)

Nicotinamide adenine dinucleotide (NAD) is a REDOX cofactor and metabolite essential for neuronal survival. Glaucoma is a common neurodegenerative disease in which neuronal levels of NAD decline. We assess the effects of nicotinamide (a precursor to ...
Optimization and validation of a UPLC-MS/MS assay for simultaneous quantification of 2,8-dihydroxyadenine, adenine, allopurinol, oxypurinol and febuxostat in human plasma

Thorsteinsdottir, Unnur A; Runólfsdóttir, Hrafnhildur L.; Eiríksson, Finnur Freyr; Ágústsd., Inger María Schweitz; Eðvarðsson, Viðar Örn; Pálsson, Runólfur; Þorsteinsdóttir, Margrét (2024-03-01)

Adenine phosphoribosyltransferase (APRT) deficiency is a rare , hereditary disorder characterized by renal excretion of 2,8-dihydroxyadenine (DHA), leading to kidney stone formation and chronic kidney disease (CKD). Treatment with a xanthine oxidoreductase ...

Now showing items 1-7 of 7

Search Opin vísindi

Browse

All of Opin vísindi
- Communities & Collections
- Authors
- Titles
- Subjects
- Departments
- School
- DOI
- Journal title

Browsing by Subject "Clinical Biochemistry"

Browsing by Subject "Clinical Biochemistry"

Search Opin vísindi

Browse

All of Opin vísindi

About

My Account