Journal
Galactosylation of serum immunoglobulin G in myasthenia gravis with different autoantibodies
Volume 83, Issue 5, September 2023, Page 348-355.
Variation of eGFR reporting and CKD equations used in the United Kingdom
Annals of Clinical Biochemistry, Ahead of Print. BackgroundUK Clinical laboratories have been routinely reporting an estimated glomerular filtration rate (eGFR) based on creatinine measurements using an eGFR equation since the early 2000s. Though there…
SUMO specific peptidase 1 decreases after induction treatment, and its reduction predicts lower disease risk, better treatment response, longer survival of acute myeloid leukemia
Volume 83, Issue 5, September 2023, Page 283-289.
Standardising the biochemical confirmation of adult male hypogonadism; a joint position statement by the Society for Endocrinology and Association of Clinical Biochemistry and Laboratory Medicine*
Annals of Clinical Biochemistry, Volume 60, Issue 4, Page 223-227, July 2023. Background: Inter-assay variation between different immunoassays and different mass spectrometry methods hampers the biochemical confirmation of male hypogonadism. Furthermor…
Serum cortisol assay performance following the 1 mg overnight dexamethasone suppression test
Annals of Clinical Biochemistry, Ahead of Print. BackgroundThe 1 mg overnight dexamethasone suppression test (ONDST) is recommended for the differential diagnosis of Cushing’s syndrome and the investigation of adrenal incidentalomas. Despite documented…
Normalized TSH strategy can improve the initial assessment of thyroid nodules
Volume 83, Issue 5, September 2023, Page 318-322.
Cardiohepatic syndrome and its prognostic predictive ability in patients with pulmonary arterial hypertension
Volume 83, Issue 5, September 2023, Page 290-298.
Validation of an indirect ELISA assay for assessment of autoantibodies against full-length TRIM21 and its individual domains
Volume 83, Issue 5, September 2023, Page 309-317.
First case of very late-onset FHL2 in Spain with two variants in the PRF1 gene
Annals of Clinical Biochemistry, Ahead of Print. Hemophagocytic lymphohistiocytosis (HLH) is a rare but fatal disorder characterized by the proliferation and infiltration of macrophages and hyperactivated T lymphocytes that escape from the physiologica…