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  1. Wilson’s Disease

    Reference work entry 2024
  2. Assessment and factors affecting quality of life among patients with Wilson’s disease

    Wilson’s disease is caused by abnormal copper metabolism resulting in deposition in various organs, including the brain, liver, and cornea, thus...

    Tingting Zhan, Yuxiang Guan, ... **ang Li in Scientific Reports
    Article Open access 15 April 2024
  3. Wilson’s Disease

    Wilson’s disease is a potentially treatable autosomal recessive disorder of copper metabolism that can manifest in various cognitive, psychiatric,...
    Chapter 2022
  4. Wilson’s Disease

    Wilson’s disease is an autosomal recessive disorder of copper metabolism. Copper accumulation in the liver, brain, and other organs results from...
    Chapter 2022
  5. Wilson’s Disease

    Wilson’s disease (WD) is an autosomal recessive metabolic disorder of impaired copper transport and excretion. Copper overload leads to tissue...
    Chapter 2022
  6. Assessment of sleep disturbance in patients with Wilson’s disease

    Background

    Wilson’s disease (WD) is frequently manifested with anxiety, depression and sleep disturbance; this investigation aimed to elucidate these...

    Zhengyang Wang, ZhiFei You in BMC Psychiatry
    Article Open access 13 March 2024
  7. Wilson’s Disease

    Wilson’s disease (WD) is a monogenetic, autosomal recessive disease caused by mutations in the ATP7B gene, which codes for the transmembrane...
    Nora V. Bergasa in Clinical Cases in Hepatology
    Chapter 2022
  8. Clinical profile of adult and pediatric patients with hepatic Wilson’s disease

    Background

    The clinical profile varies in patients with Wilson’s disease (WD). There is paucity of data regarding adult and pediatric patients with...

    Sanjay Kumar, Mohd Irtaza, ... Akash Shukla in Indian Journal of Gastroenterology
    Article 01 April 2024
  9. A case of Wilson’s disease combined with intracranial lipoma and dysplasia of the corpus callosum with review of the literature

    Background

    Wilson’s disease (WD) is an inherited disorder of copper metabolism. Agenesis of the corpus callosum is the complete or partial absence of...

    Liangjie Zhang, Ling Zhu, ... Xun Wang in BMC Neurology
    Article Open access 25 January 2024
  10. Membranous nephropathy caused by dimercaptosuccinic acid in a patient with Wilson’s disease: a case report and literature review

    Background

    Dimercaptosuccinic acid (DMSA) therapy is a kind of chelation therapy for patients with Wilson ‘s disease (WD). While there have been...

    **ang Li, Feng**n Hu, Gaosi Xu in BMC Nephrology
    Article Open access 26 May 2023
  11. Correlation between neuroimaging, neurological phenotype, and functional outcomes in Wilson’s disease

    Introduction

    Wilson’s disease (WD) is associated with a variety of movement disorders and progressive neurological dysfunction. The aim of this study...

    João Moura, Catarina Pinto, ... Marina Magalhães in Neurological Sciences
    Article 31 January 2024
  12. Rare co-occurrence of multiple sclerosis and Wilson’s disease – case report

    Background

    Wilson’s disease is a hereditary disorder of copper metabolism resulting mainly in hepatic, neurological, and psychiatric symptoms....

    Katalin Despotov, Péter Klivényi, ... Cecília Rajda in BMC Neurology
    Article Open access 16 May 2022
  13. Early neurological deterioration in Wilson’s disease: a systematic literature review and meta-analysis

    Introduction

    Neurological deterioration, soon after anti-copper treatment initiation, is problematic in the management of Wilson’s disease (WD) and...

    Agnieszka Antos, Anna Członkowska, ... Tomasz Litwin in Neurological Sciences
    Article Open access 14 June 2023
  14. Systemic lupus erythematosus combined with Wilson’s disease: a case report and literature review

    Background

    Systemic lupus erythematosus (SLE) and Wilson’s disease (WD) are both systemic diseases that can affect multiple organs in the body. The...

    Zhenle Yang, Qian Li, ... Shuzhen Sun in BMC Pediatrics
    Article Open access 15 April 2024
  15. Long-term outcome of patients with neurological form of Wilson’s disease compliant to the de-coppering treatment

    Background

    A substantial proportion of Wilson’s disease (WD) patients exhibit residual neurological symptoms. Data on the prognostic value of initial...

    Iva Stanković, Čarna Jovanović, ... Vladimir Kostić in Journal of Neurology
    Article 05 April 2023
  16. Serum neurofilament light chain and initial severity of neurological disease predict the early neurological deterioration in Wilson’s disease

    Background

    In Wilson’s disease (WD), early neurological deterioration after treatment initiation is associated with poor outcomes; however, data on...

    Tjalf Ziemssen, Lukasz Smolinski, ... Tomasz Litwin in Acta Neurologica Belgica
    Article Open access 13 September 2022
  17. Construction of a nomogram for predicting compensated cirrhosis with Wilson’s disease based on non-invasive indicators

    Background

    Wilson’s disease (WD) often leads to liver fibrosis and cirrhosis, and early diagnosis of WD cirrhosis is essential. Currently, there are...

    Yan Li, **g ** Wang, **aoli Zhu in BMC Medical Imaging
    Article Open access 16 April 2024
  18. Adherence to medical treatment for Wilson’s disease in children and adolescents: a cohort study from Turkey

    Background

    This study aimed to assess medication adherence and demographic, clinical, and psychopathological parameters such as quality of life,...

    Mehmet Akif Göktaş, Nadir Yalcin in Orphanet Journal of Rare Diseases
    Article Open access 07 March 2024
  19. Sleep disorders in Wilson’s disease: a questionnaire study

    Objective

    To examine the clinical characteristics and influencing factors related to sleep disorders in patients with Wilson’s disease (WD), and...

    Zhifei You, Hui Xu, ... Zhengchen You in Neurological Sciences
    Article 15 September 2022
  20. Normal Ceruloplasmin-Suspected Wilson’s

    Explanation for the finding of a normal ceruloplasmin in a patient with Wilson’s. How to confirm the diagnosis.
    Chapter 2023
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