Results 1 to 10 of about 13,629 (129)

Role of serum ceruloplasmin in the diagnosis of Wilson's disease: A large Chinese study [PDF]

open access: yesFrontiers in Neurology, 2022
BackgroundConventionally, serum ceruloplasmin levels below the lower reference limit (0. 20 g/L) is considered a diagnostic cutoff point for Wilson's disease (WD).
Yue Yang   +9 more
doaj   +4 more sources

Assessment of the diagnostic value of serum ceruloplasmin for Wilson’s disease in children [PDF]

open access: yesBMC Gastroenterology, 2022
Background Serum ceruloplasmin is one of the major diagnostic parameters for Wilson’s disease (WD). Age and gender difference of serum ceruloplasmin remain controversy.
Xinshuo Lu   +12 more
doaj   +2 more sources

Assessing whether serum ceruloplasmin promotes non-alcoholic steatohepatitis via regulating iron metabolism [PDF]

open access: yesJournal of Medical Biochemistry, 2023
Background: Non-alcoholic steatohepatitis (NASH) is a progressive form of non-alcoholic fatty liver disease (NAFLD). The diagnostic gold standard for detecting NASH still relies upon an invasive pathological biopsy.
Xia Ziqiang   +6 more
doaj   +2 more sources

Plasma zinc, copper and serum ceruloplasmin levels of autism spectrum disorder children in Bangladesh [PDF]

open access: yesHeliyon, 2023
Neural and cognitive processes require zinc and copper homeostasis and a normal zinc/copper ratio. Ceruloplasmin, an intrinsic antioxidant protein, maintains copper homeostasis, which might also influence autism spectrum disorder (ASD).
Umme Raihan Siddiqi   +6 more
doaj   +2 more sources

Elevated Serum Ceruloplasmin Levels Are Associated with Higher Impulsivity in People with Parkinson’s Disease [PDF]

open access: yesParkinson's Disease, 2020
Background. Heightened impulsivity has been reported in a subset of people with Parkinson’s disease (PwP) and is considered a risk factor for the development of impulse control disorders (ICDs).
Megan C. Bakeberg   +12 more
doaj   +2 more sources

Pediatric Wilson Disease in Sudan: A Rare Case, Sudan Conflict and Diagnostic Challenges. [PDF]

open access: yesClin Case Rep
ABSTRACT Wilson disease is rarely reported among African children. Wilson disease is due to a mutation in ATP7B on an autosomal recessive pattern, which causes defective copper excretion and copper accumulation in tissues such as liver and brain.
Mohammed AAA   +8 more
europepmc   +2 more sources

Association of serum trace elements with non-invasive fibrosis scores in metabolic dysfunction-associated steatotic liver disease [PDF]

open access: yesScientific Reports
Liver biopsy is not a routine screening tool for detecting fibrosis progression in metabolic dysfunction-associated steatotic liver disease (MASLD). Noninvasive methods based on serum biomarkers are used instead.
Erfan Banisefid   +5 more
doaj   +2 more sources

Study of serum copper and ceruloplasmin levels in Egyptian autistic children

open access: yesEgyptian Journal of Medical Human Genetics, 2018
Background: Autism is a behaviorally defined neurodevelopmental disorder of unknown etiology. Objective: To assess serum copper and ceruloplasmin levels in Egyptian autistic children patients.
Farida El-Baz   +2 more
doaj   +3 more sources

Study of serum ceruloplasmin and zinc in type 2 diabetes mellitus

open access: yesZanco Journal of Medical Sciences, 2021
Background and objective: Ceruloplasmin is the major copper-carrying protein in the blood and plays a role in iron metabolism. Zinc is an essential trace element for human health, which activates about 200 enzymes.
Amanj Zrar Hasan   +2 more
doaj   +1 more source

Serum Ceruloplasmin Level as a Predictor for the Progression of Diabetic Nephropathy in Korean Men with Type 2 Diabetes Mellitus [PDF]

open access: yesDiabetes & Metabolism Journal, 2015
BackgroundOxidative stress is known to be associated with progression of diabetic kidney disease. Ceruloplasmin acts as a pro-oxidant under conditions of severe oxidative stress.
Min Jung Lee   +6 more
doaj   +1 more source

Home - About - Disclaimer - Privacy