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
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.
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
Case Report on Acquired Hepatocerebral Degeneration
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
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
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
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
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
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
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

