Exploring the potential of trientine tetrahydrochloride in the treatment of Wilson disease by Nikita Sharma, Debashree Debasish Das, Pooja A Chawla

Subjects: “…Wilson disease…”
Get full text

Benefits and drawbacks of current copper chelators in Wilson disease by Ioan-Cristian Lupescu, Maria Speranta Iacob, Razvan Iacob, Daniela Anghel, Octavia Adriana Dulamea, Crisanda Vilciu, Liliana Gheorghe

Subjects: “…wilson disease…”
Get full text

Research progress in stem cell therapy for Wilson disease by Xianlang Xiong, Ce Gao, Xiangying Meng, Aihui Liu, Xin Gong, Yi Sun

Subjects: Get full text

Insomnia as a rare neuropsychiatric presentation of Wilson disease by Pang, Nicholas Tze Ping, Mat Rosly, Mohamed S

Get full text
Get full text

The spectrum of liver presentation in wilson's disease: a literature review by Adela TURCANU, Veronica CUMPATA

Subjects: “…wilson disease…”
Get full text

Clinical, biochemical and molecular characterization of Wilson's disease in Moroccan patients by Karima Lafhal, Es-said Sabir, Abdelmalek Hakmaoui, Miloud Hammoud, Abdelmohcine Aimrane, Samira Najeh, Imane Assiri, Abdelaati Berrachid, Najwa Imad, Chaima Ait Boujemaa, Faissal Aziz, Fatima Zahra El Hanafi, Abdessamad Lalaoui, Hasna Aamri, Iryna Boyko, Ana Sánchez-Monteagudo, Carmen Espinós, Imane Ait Sab, Nisrine Aboussair, Aicha Bourrahouat, Naima Fdil

Subjects: “…Wilson disease…”
Get full text

Low Copper Diet—A Therapeutic Option for Wilson Disease? by Ulrike Teufel-Schäfer, Christine Forster, Nikolaus Schaefer

Get full text

The mutation spectrum and ethnic distribution of Wilson disease, a review by Zahra Beyzaei, Arman Mehrzadeh, Niko Hashemi, Bita Geramizadeh

“…Wilson's disease is a complicated medical condition caused by the accumulation of copper, mostly in the liver and brain. …”
Get full text

Successful Treatment of Hypersplenism in Wilson's Disease by Partial Splenic Embolization by Liang-Yong Li, Huai-Zhen Chen, Yuan-Cheng Bao, Qing-Sheng Yu, Wen-Ming Yang

Subjects: Get full text

Management and Outcomes of Wilson Disease in Pregnancy: A Case Report by Zahra Moaazeni, Danial Soltani, Mahnaz Boroumand Rezazadeh, Mohammad Reza Rouhbakhsh Zahmatkesh, Neda Davaryari

Subjects: Get full text

Serum fetuin-A is decreased in cirrhotic patients with Wilson's disease. by Krisztián Vörös, Bernadett Márkus, Klára Atzél, Ferenc Szalay, László Gráf, Dániel Németh, Tamás Masszi, Péter Torzsa, László Kalabay

“…<h4>Introduction</h4>Wilson's disease may lead to cirrhosis, but timely medical treatment could slow down its progression. …”
Get full text

Diagnosis of Wilson Disease and Its Phenotypes by Using Artificial Intelligence by Valentina Medici, Anna Czlonkowska, Tomasz Litwin, Cecilia Giulivi

Subjects: “…Wilson disease…”
Get full text

Genomic studies of gene expression: regulation of the Wilson disease gene. by Bochukova, E, Jefferson, A, Francis, M, Monaco, A

“…We describe the utilization of a BAC construct to study gene regulation in a tissue culture-based system, using a 170-kb clone containing the entire Wilson disease (WND) locus as a model. A second BAC construct that lacked a putative negatively regulating promoter sequence was created. …”

REGIONAL LOCALIZATION OF CHROMOSOME-13 CLONES AND THEIR APPLICATION TO WILSON DISEASE by Bull, P, Barwell, J, Pautler, S, Lalande, M, Cox, D

Generalized Dystonia as Presenting Feature of Wilson Disease: A Case Report by Akansha Anushree MBBS, Sudesh Kumar MD, Piyali Bhattacharya MD, Siddharth Tripathi MBBS, Nandita Chattopadhyay DNB

“…MRI brain showed B/L putamen hyperintensity and panda sign suggestive of Wilson disease. After the diagnosis of Wilson disease was made, patient was treated with penicillamine and zinc. …”
Get full text

Status epilepticus in a case with wilson's disease during Dpencillamine treatment by A Kocer, R Alp, M Gümüs, M Gümüs, Börü Türk

Subjects: Get full text

Machine learning for detecting Wilson's disease by amplitude of low-frequency fluctuation by Bing Zhang, Jingjing Peng, Hong Chen, Wenbin Hu

Subjects: “…Wilson's disease…”
Get full text

Structures of the human Wilson disease copper transporter ATP7B by Guo-Min Yang, Lingyi Xu, Rou-Min Wang, Xin Tao, Zi-Wei Zheng, Shenghai Chang, Demin Ma, Cheng Zhao, Yi Dong, Shan Wu, Jiangtao Guo, Zhi-Ying Wu

“…Mutants of ATP7B cause Wilson disease (WD), an autosomal recessive disorder of copper metabolism. …”
Get full text

Wilson disease and Menkes disease: new handles on heavy-metal transport. by Bull, P, Cox, D

“…Recently, however, two human diseases that disrupt copper transport, Menkes disease and Wilson disease, were found to be caused by mutations in two closely related genes, MNK and WND, which encode proteins belonging to the P-type ATPase family of cation transporters. …”

Mapping of the mouse homologue of the Wilson disease gene to mouse chromosome 8. by Reed, V, Williamson, P, Bull, P, Cox, D, Boyd, Y

“…ATP7B, the gene altered in Wilson disease (WD) patients, lies in a block of homology shared between human chromosome 13q14 and the central region of mouse chromosome 14. …”