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Sleep disorders in Wilson disease: a systematic review and meta-analysis.
Xu J, Deng Q, Qin Q, Vgontzas AN, Basta M, Xie C, Li Y. Xu J, et al. J Clin Sleep Med. 2020 Feb 15;16(2):219-230. doi: 10.5664/jcsm.8170. Epub 2020 Jan 13. J Clin Sleep Med. 2020. PMID: 31992405 Free PMC article.
STUDY OBJECTIVES: Wilson disease (WD) is an autosomal recessive inherited disorder of copper metabolism resulting in pathologic accumulation of copper in many organs and tissues. ...
STUDY OBJECTIVES: Wilson disease (WD) is an autosomal recessive inherited disorder of copper metabolism resulting in pathologi …
A Systematic Review and Meta-Analysis of the R778L Mutation in ATP7B With Wilson Disease in China.
Xue Z, Chen H, Yu L, Jiang P. Xue Z, et al. Pediatr Neurol. 2023 Aug;145:135-147. doi: 10.1016/j.pediatrneurol.2023.04.026. Epub 2023 May 8. Pediatr Neurol. 2023. PMID: 37354629
BACKGROUND: Wilson disease (WD) is a hereditary disorder of copper metabolism, caused by mutations in the ATP7B gene. ...We then conducted a systematic review and meta-analysis in databases, using the keywords Wilson disease and R778L mutation. RESULTS …
BACKGROUND: Wilson disease (WD) is a hereditary disorder of copper metabolism, caused by mutations in the ATP7B gene. ...We th …
Systematic review: clinical efficacy of chelator agents and zinc in the initial treatment of Wilson disease.
Wiggelinkhuizen M, Tilanus ME, Bollen CW, Houwen RH. Wiggelinkhuizen M, et al. Aliment Pharmacol Ther. 2009 May 1;29(9):947-58. doi: 10.1111/j.1365-2036.2009.03959.x. Aliment Pharmacol Ther. 2009. PMID: 19210288 Free article. Review.
BACKGROUND: No consensus is available on the optimal initial treatment in Wilson disease. AIM: To assess systematically the available literature of treatment in newly presenting patients with a presymptomatic, hepatic or neurological presentation of Wilson …
BACKGROUND: No consensus is available on the optimal initial treatment in Wilson disease. AIM: To assess systematically the av …
Cognitive and psychiatric phenotypes of movement disorders in children: a systematic review.
Ben-Pazi H, Jaworowski S, Shalev RS. Ben-Pazi H, et al. Dev Med Child Neurol. 2011 Dec;53(12):1077-84. doi: 10.1111/j.1469-8749.2011.04134.x. Epub 2011 Sep 27. Dev Med Child Neurol. 2011. PMID: 21950517 Free article. Review.
Symptoms of depression and anxiety were more frequent in individuals with idiopathic dystonia. Affective disorders were suggestive of Wilson disease. Cognitive decline was common in children with juvenile Huntington disease. ...
Symptoms of depression and anxiety were more frequent in individuals with idiopathic dystonia. Affective disorders were suggestive of Wil …
Serum glial fibrillary acidic protein is a body fluid biomarker: A valuable prognostic for neurological disease - A systematic review.
Heimfarth L, Passos FRS, Monteiro BS, Araújo AAS, Quintans Júnior LJ, Quintans JSS. Heimfarth L, et al. Int Immunopharmacol. 2022 Jun;107:108624. doi: 10.1016/j.intimp.2022.108624. Epub 2022 Mar 4. Int Immunopharmacol. 2022. PMID: 35255304 Review.
A total of16 different neurological disorders that have plasmatic GFAP levels as a possible biomarker for the disease were described in the articles, being: multiple sclerosis, frontotemporal lobar degeneration, Alzheimer's disease, Parkinson disease, COVID-19, epileptic seizures …
A total of16 different neurological disorders that have plasmatic GFAP levels as a possible biomarker for the disease were described in the …
Comparative effectiveness of common therapies for Wilson disease: A systematic review and meta-analysis of controlled studies.
Appenzeller-Herzog C, Mathes T, Heeres MLS, Weiss KH, Houwen RHJ, Ewald H. Appenzeller-Herzog C, et al. Liver Int. 2019 Nov;39(11):2136-2152. doi: 10.1111/liv.14179. Epub 2019 Jul 10. Liver Int. 2019. PMID: 31206982
BACKGROUND & AIMS: Wilson disease (WD) is a rare disorder of copper metabolism. The objective of this systematic review was to determine the comparative effectiveness and safety of common treatments of WD. ...
BACKGROUND & AIMS: Wilson disease (WD) is a rare disorder of copper metabolism. The objective of this systematic review wa …
The copper radioisotopes: a systematic review with special interest to 64Cu.
Niccoli Asabella A, Cascini GL, Altini C, Paparella D, Notaristefano A, Rubini G. Niccoli Asabella A, et al. Biomed Res Int. 2014;2014:786463. doi: 10.1155/2014/786463. Epub 2014 May 7. Biomed Res Int. 2014. PMID: 24895611 Free PMC article. Retracted. Review.
In recent years, Cu isotopes have been linked to antibodies, proteins, peptides, and nanoparticles for preclinical and clinical research; pathological conditions that influence Cu metabolism such as Menkes syndrome, Wilson disease, inflammation, tumor growth, metast …
In recent years, Cu isotopes have been linked to antibodies, proteins, peptides, and nanoparticles for preclinical and clinical research; pa …
Diagnostic and treatment implications of psychosis secondary to treatable metabolic disorders in adults: a systematic review.
Bonnot O, Klünemann HH, Sedel F, Tordjman S, Cohen D, Walterfang M. Bonnot O, et al. Orphanet J Rare Dis. 2014 Apr 28;9:65. doi: 10.1186/1750-1172-9-65. Orphanet J Rare Dis. 2014. PMID: 24775716 Free PMC article. Review.
DATA SOURCES: Published literature on MEDLINE was assessed regarding diseases of homocysteine metabolism (DHM; cystathionine beta-synthase deficiency [CbS-D] and homocysteinemia due to methyltetrahydrofolate reductase deficiency [MTHFR-D]), urea cycle disorders (UCD), acute porph …
DATA SOURCES: Published literature on MEDLINE was assessed regarding diseases of homocysteine metabolism (DHM; cystathionine beta-synthase d …
Elastosis perforans serpiginosa: causes and associated disorders.
Montesu MA, Onnis G, Gunnella S, Lissia A, Satta R. Montesu MA, et al. Eur J Dermatol. 2018 Aug 1;28(4):476-481. doi: 10.1684/ejd.2018.3355. Eur J Dermatol. 2018. PMID: 30129530
Herein, we report a systematic review of the literature, as well as a case of a 41-year-old woman with Wilson disease treated with penicillamine (PCM), who developed EPS after 11 years of drug intake. ...
Herein, we report a systematic review of the literature, as well as a case of a 41-year-old woman with Wilson disease treated …