Results 41 to 50 of about 1,024,802 (210)

Evaluation of systemic consequences of brachycephalic obstructive airway syndrome in dogs

open access: yesVeterinary Record, EarlyView.
Abstract Background Brachycephalic obstructive airway syndrome (BOAS) results from upper airway anatomical abnormalities and may cause systemic effects depending on severity. Methods A prospective, case‒control and observational study was conducted.
Andréia Coutinho Facin   +11 more
wiley   +1 more source

Functional relevance of ceruloplasmin mutations in Parkinson's disease.

open access: yes, 2005
peer reviewedIncreased iron levels of the substantia nigra and the discovery of ceruloplasmin mutations in patients with Parkinson's disease (PD) imply impaired iron metabolism in this neurodegenerative disorder.
Behnke, Stefanie   +8 more
core   +1 more source

Evaluation of salivary ceruloplasmin for the diagnosis of Wilson’s disease

open access: yesScientific Reports
The serum ceruloplasmin assay is the most commonly used test for diagnosing Wilson’s disease (WD). Despite the utility of non-invasive tests for diagnosing WD, no such tests have been developed.
Nian Zhang   +10 more
doaj   +1 more source

Serum Ceruloplasmin in Pre-eclampsia: A Case–Control Study in a Tertiary Health Centre in Southwest Nigeria

open access: yesNigerian Postgraduate Medical Journal
Background: Pre-eclampsia is a pregnancy disorder linked with increased maternal and perinatal complications. An imbalance between free radical-induced lipid peroxidation and the antioxidant system may contribute to its pathogenesis.
Joy Onyinyechi Chionuma   +4 more
doaj   +1 more source

Cardiometabolic Protein Profile Changes During Gender‐Affirming Hormone Therapy: A Prospective Clinical Study

open access: yesClinical Endocrinology, EarlyView.
ABSTRACT Objective Cardiovascular disease (CVD) risk is elevated in transgender individuals during gender‐affirming hormone therapy (GAHT) with expected different mechanisms between T‐ and E2‐based GAHT. We investigated prospective changes in cardiometabolic proteins relating to complement, inflammation, and transport during GAHT.
Emilie Bukh Madsen   +12 more
wiley   +1 more source

Serum ceruloplasmin levels for early detection of oral precancer and oral cancer—a systematic review and meta-analysis

open access: yesJournal of Oral Medicine and Oral Surgery
Introduction: Oral squamous cell carcinoma (OSCC) is the most prevalent malignancy of the head and neck region. It frequently develops from oral potentially malignant disorders such as leukoplakia and oral submucous fibrosis, both of which carry a ...
Joseph Marina, Naik Veena V.
doaj   +1 more source

A Study of some biochemical parameters in patients with - thalassemia

open access: yesمجلة بغداد للعلوم, 2008
Serum levels of iron,copper,ceruloplasmin and transferrine were estimated in three groups of patients with ?- thalassemia: 24 patients have splenectomy thalassemia major, 29 patients have non splenectomy thalassemia major and 19 patients have thalassemia
Baghdad Science Journal
doaj   +1 more source

TMEM199-Congenital Disorder of Glycosylation With Novel Phenotype and Genotype in a Chinese Boy

open access: yesFrontiers in Genetics, 2022
Background: TMEM199-congenital disorder of glycosylation (TMEM199-CDG) is a rare autosomal recessive inherited disease characterized by chronically elevated serum transaminase, decreased serum ceruloplasmin, steatosis and/or fibrosis, TMEM199 mutation ...
Yuan Fang   +5 more
doaj   +1 more source

CLINICAL AND EXPERIMENTAL STUDIES OF SERUM CERULOPLASMIN I

open access: yesNihon Naika Gakkai Zasshi, 1965
中福神経と銅代謝の関係が問題にされ,間脳の刺激により血清銅の増減が報告されている.著者は血清銅の大部分を占めるceruloplasmin(CPと略す)の変動に自律神経系が関与しているものと考えられるので,自律神経毒薬物としてadrenalin, insulin, pilocarpinの皮下注射および髄腔内空気注入の方法でヒトおよび家兎の血清CPの変動を調べた. adrenalin, insulinの皮下注射でヒトおよび家兎の血清CPは増加したが, pilocarpinの皮下注射では家兎の血清CPの変動をみなかつた、髄腔内空気注入によつてはCPの増加を認め, adrenalin, insulinによる刺激に比して前値に戻る時間が延長していた.
openaire   +3 more sources

A De Novo ATP1A3 p.Arg995His Variant in a Patient With an Adult‐Onset Primary Lateral Sclerosis‐Like Syndrome

open access: yesClinical Genetics, EarlyView.
A 43‐year‐old woman developed a progressive adult‐onset upper motor neuron syndrome fulfilling the clinical criteria for primary lateral sclerosis (PLS), with mild cerebellar involvement. Genetic testing identified a de novo ATP1A3 p.Arg995His variant affecting a highly conserved residue within the transmembrane M8 domain.
Pablo Hernandez‐Vitorique   +4 more
wiley   +1 more source

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