Menkes and Wilson diseases. by Monaco, A, Chelly, J

Postpartum Diagnosed Wilsons Disease by Serpil Aydogmus, Serenat Eris, Secil Kurtulmus, Huseyin Aydogmus, Emre Ekmekci, Fatih Demir, Sefa Kelekci

Subjects: “…wilsons disease…”
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Wilsons Disease: Diagnostic Approach by Hakan Gelincik, Filiz Koc

Subjects: “…Wilson's disease…”
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Wilson's Disease Presenting With Pancytopenia by Can Acıpayam, Ali Altunay, Nilüfer İlhan, Nesrin Atçı

“…Pancytopenia is a rare initial symptom of Wilson Disease. An 11-year-old female presented with pancytopenia. …”
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Monitoring of Copper in Wilson Disease by Grażyna Gromadzka, Marta Grycan, Adam M. Przybyłkowski

Subjects: “…Wilson disease…”
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Haplotype studies in Wilson disease. by Thomas, G, Bull, P, Roberts, E, Walshe, J, Cox, D

“…In 51 families with Wilson disease, we have studied DNA haplotypes of dinucleotide repeat polymorphisms (CA repeats) in the 13q14.3 region, to examine these markers for association with the Wilson disease gene (WND). …”

Cloning the Wilson disease gene. by Chelly, J, Monaco, A

Wilson's disease presenting with rapidly progressive visual loss: another neurologic manifestation of Wilson's disease? by Gow, P, Peacock, SE, Chapman, R

“…Wilson's disease (WD) is a rare autosomal recessive disorder of copper metabolism resulting in copper-induced tissue damage that primarily involves the liver and central nervous system. …”

Schizophrenia-like disorder in Wilson's disease by I. D. Spirina, E. S. Fawzy, Yu. N. Shevchenko, A. V. Shornikov, A. V. Smolianova, A. N. Nikolaychik

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Wilson's Disease update: An Indian perspective by Niraj Kumar, L K Prashant, Vinay Goyal

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Management of wilson disease: The quest continues by Gautam Kamila, Biswaroop Chakrabarty

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Kayser–Fleischer rings: The pathognomonic for Wilson's disease by Priyanka Singh, Bachaspati Subedi, Devraj Mahato, Mitesh Karn

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New developments in the management of Wilson's disease in children by Tudor Lucian Pop, Alina Grama

Subjects: “…Wilson's disease…”
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Construction of diagnostic prediction model for Wilson's disease by Yao Wang, Yao Wang, Yulian Li, Linting Xun, Zhengji Song

“…BackgroundWilson's disease, also known as hepatolenticular degeneration, is a rare human autosomal recessive inherited disorder of copper metabolism. …”
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“Face of the Giant Panda” Sign in Wilson Disease by Mehmet Atalar, Nisa Başpınar

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HAPLOTYPES IN WILSON DISEASE - IMPLICATIONS FOR MUTATIONAL ANALYSIS by Thomas, G, Roberts, E, Bull, P, Cox, D

Structural and Functional Cardiac Changes in Children with Wilson Disease by Magd A. Kotb, Fatma Al Zahraa Mostafa, Ahmed M. Badr, Aya S. Hegazy, Mohamed S. Eid, Nahla I. Sabry, Radwa Shamma

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Resistance Training in Wilson Disease: A Case Study by Zahra Chakeri, Saeed Talebian

Subjects: “…Wilson disease…”
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Psychosis in Wilson's disease: A rare case presentation by Kota Raga Sumedha, Anitha Rayirala, Rajshekhar Bipeta

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P198: Mutation spectrum of Wilson disease in Taiwan by Yu-Hsuan Huang, Chin-Hsien Lin, Ni-Chung Lee, Yin-Hsiu Chien, Huey-Ling Chen, Wuh-Liang Hwu, Yen-Hsuan Ni

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