Zobrazeno 1 - 10
of 328
pro vyhledávání: '"Serum ceruloplasmin"'
Autor:
Kalyan Bhattacharya, Bindu Thankappan
Publikováno v:
Annals of Indian Academy of Neurology, Vol 25, Iss 1, Pp 43-53 (2022)
Wilson's disease (WD) is an autosomal recessive disorder due to ATP7B gene mutation, resulting in defective copper metabolism, with liver and brain being primarily affected. Being a treatable disorder, early diagnosis and proper management of WD may
Externí odkaz:
https://doaj.org/article/91740fa06431426ba53655ad9c338e34
Autor:
Yue Yang, Wenjie Hao, Taohua Wei, LuLu Tang, Nannan Qian, Yulong Yang, Hu Xi, Shijie Zhang, Wenming Yang
Publikováno v:
Frontiers in Neurology, Vol 13 (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). However, the lower reference limit varies with assay methodologies and the individuals
Externí odkaz:
https://doaj.org/article/57179efece804dc880f0820886935826
Abnormalities in Copper Status Associated with an Elevated Risk of Parkinson’s Phenotype Development
Autor:
Marina N. Karpenko, Zamira M. Muruzheva, Ekaterina Yu. Ilyechova, Polina S. Babich, Ludmila V. Puchkova
Publikováno v:
Antioxidants, Vol 12, Iss 9, p 1654 (2023)
In the last 15 years, among the many reasons given for the development of idiopathic forms of Parkinson’s disease (PD), copper imbalance has been identified as a factor, and PD is often referred to as a copper-mediated disorder. More than 640 paper
Externí odkaz:
https://doaj.org/article/652c5c090b284081947f06d6171d95d1
Publikováno v:
Egyptian Liver Journal, Vol 11, Iss 1, Pp 1-4 (2021)
Abstract Background Wilson’s disease is a multisystem disorder with predominant clinical symptoms depending on the site of copper deposition in the body. Hepatic presentation is usually seen in the younger age group. And pancreatitis is rarely asso
Externí odkaz:
https://doaj.org/article/09e00ed92b794771a23d88c2bdb38785
Publikováno v:
Zanco Journal of Medical Sciences, Vol 25, Iss 1, Pp 480-485 (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. This study aimed to evaluate the se
Externí odkaz:
https://doaj.org/article/d4ba8f35a8ce4769a736cf6f1bce6ea7
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 5, Pp 652-663 (2021)
Wilson's disease (WD) is an autosomal recessive disorder due to ATP7B gene mutation, resulting in defective copper metabolism, with the liver and brain being primarily affected. WD being a treatable disorder, early diagnosis and proper management may
Externí odkaz:
https://doaj.org/article/61d0de273be946338168886d64dcd1f9
Publikováno v:
Perspectives In Medical Research, Vol 8, Iss 3, Pp 70-73 (2020)
Background : Psoriasis is one of the common diseases diagnosed in dermatology clinics. It is characterized by erythematous and sharply demarcated papules covered by silvery micaceous scales. Although, etiology is an unclear genetic predisposition
Externí odkaz:
https://doaj.org/article/8892065015574ff3a15dd86e7f03ba5c
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 13, Iss 3, Pp OD08-OD10 (2019)
Human Parvovirus infection is a rare condition causing encephalitis as well as pancytopenia. Similarly patient of Wilson disease presenting as hepatic encephalopathy as an initial manifestation is also a rare phenomenon. A previously healthy 20-year-
Externí odkaz:
https://doaj.org/article/d2b2ea1ba7074be480c7fe65092a0a82
Autor:
MI Khan, K Prashant
Publikováno v:
Perspectives In Medical Research, Vol 8, Iss 3, Pp 70-73 (2020)
Background : Psoriasis is one of the common diseases diagnosed in dermatology clinics. It is characterized by erythematous and sharply demarcated papules covered by silvery micaceous scales. Although, etiology is an unclear genetic predisposition see
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fb72392633d86b1cea65fe79fde269b
https://doi.org/10.47799/pimr.0803.15
https://doi.org/10.47799/pimr.0803.15
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