Results 61 to 70 of about 1,024,802 (210)

Table_2_Role of serum ceruloplasmin in the diagnosis of Wilson's disease: A large Chinese study.doc

open access: yes, 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 (52715)   +8 more
core   +1 more source

Clinical impact of ceruloplasmin levels at ANCA-associated vasculitis diagnosis.

open access: yesPLoS ONE
ObjectivesCeruloplasmin is an inhibitor of myeloperoxidase (MPO) activity that plays an important role in the pathophysiology of anti-neutrophil cytoplasmic antibody-associated vasculitis (AAV). This study aimed to evaluate the prognostic impact of serum
Louis Camboulive   +10 more
doaj   +1 more source

Aspartate aminotransferase at large—A case of disappearing macro‐aspartate aminotransferase in a child

open access: yes
JPGN Reports, EarlyView.
Aaron Weston   +7 more
wiley   +1 more source

Case Report on Acquired Hepatocerebral Degeneration

open access: yesProgress in Neurology and Psychiatry, Volume 30, Issue 4, November 2026.
ABSTRACT Acquired hepatocerebral degeneration (AHD) is an uncommon neurological manifestation of chronic liver disease, most often associated with portosystemic shunting. The disorder is characterised by a combination of movement abnormalities, cognitive decline, and psychiatric disturbance. Manganese accumulation within the basal ganglia, secondary to
Aamir Khan, Odai Jumma, Taram Nayab
wiley   +1 more source

Image_1_Role of serum ceruloplasmin in the diagnosis of Wilson's disease: A large Chinese study.tif

open access: yes, 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 (52715)   +8 more
core   +1 more source

Determination of Ceruloplasmin Oxidase in Serum

open access: yesExperimental Biology and Medicine, 1960
SummaryA method for determination of ceruloplasmin in serum is presented in which rate of oxidation of p-phenylenediamine is measured spectrophotometrically or photometrically. Correction for catalytic oxidation by free metals present is made by reading the test against a serum blank in which enzymatic activity is inhibited by azide.
R. J. Henry   +3 more
openaire   +1 more source

Progressive Parkinsonism in PPP2R5D‐Related Neurodevelopmental Disorder

open access: yesAnnals of Clinical and Translational Neurology, Volume 13, Issue 10, Page 2161-2165, October 2026.
ABSTRACT PPP2R5D‐related neurodevelopmental disorder (Houge–Janssens syndrome type 1) is a rare autosomal dominant condition characterized by macrocephaly, intellectual disability, and epilepsy. Progressive parkinsonism is an emerging adult phenotype that neurologists should be aware of since timely genetic diagnosis opens the door to disease‐modifying
Katerina Bernardi   +6 more
wiley   +1 more source

Table_1_Role of serum ceruloplasmin in the diagnosis of Wilson's disease: A large Chinese study.doc

open access: yes, 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 (52715)   +8 more
core   +1 more source

Study of copper and ceruloplasmin in hypothyroidism and Grave’s hyperthyroidism as compared to euthyroidism: Hospital-based case–control study

open access: yesMRIMS Journal of Health Sciences
Background: Hypothyroidism was highly prevalent in India, with 10.95% affected patients as compared with only 2% in the United Kingdom and 4·6% in the USA. The prevalence of Hyperthyroidism was found to be 1.6%.
Vinayak Ganesh Bhat   +4 more
doaj   +1 more source

Glymphatic System Dysfunction and its Associated Factors in Wilson's Disease: A DTI–ALPS Study

open access: yesBrain and Behavior, Volume 16, Issue 10, October 2026.
Glymphatic function, assessed by DTI‐ALPS index, was impaired in neurological Wilson's disease compared with hepatic phenotype and controls. Age, AST, and UWDRS‐I score independently predicted dysfunction, linking neurodegeneration, liver injury, and altered glymphatic activity. ABSTRACT Background Wilson's disease (WD) is a genetic disorder of copper (
Ling Zhu   +14 more
wiley   +1 more source

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