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International Journal of Neuroscience Volume 121, 2011 - Issue 1
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Research Article

Influence of IL-1RN Intron 2 Variable Number of Tandem Repeats (VNTR) Polymorphism on the Age at Onset of Neuropsychiatric Symptoms in Wilson's Disease

Grażyna GromadzkaInstitute of Psychiatry and Neurology, Second Department of Neurology, Warsaw, Poland, and Medical University, Department of Experimental and Clinical Pharmacology, Warsaw, Poland
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Anna CzłonkowskaInstitute of Psychiatry and Neurology, Second Department of Neurology, Warsaw, Poland, and Medical University, Department of Experimental and Clinical Pharmacology, Warsaw, PolandCorrespondence[email protected]
Pages 8-15 | Received 22 Jul 2010, Published online: 20 Jan 2011

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Grażyna Gromadzka, Diana Weronika Wierzbicka, Adam Przybyłkowski & Tomasz Litwin. (2022) Effect of homeostatic iron regulator protein gene mutation on Wilson's disease clinical manifestation: original data and literature review. International Journal of Neuroscience 132:9, pages 894-900.
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Articles from other publishers (18)

Grażyna Gromadzka, Maria Bendykowska & Adam Przybyłkowski. (2023) Wilson’s Disease—Genetic Puzzles with Diagnostic Implications. Diagnostics 13:7, pages 1287.
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Hui Wang, Li-San Wang, Gerard Schellenberg & Wan-Ping Lee. (2023) The role of structural variations in Alzheimer’s disease and other neurodegenerative diseases. Frontiers in Aging Neuroscience 14.
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Ümit Özkan, Firdevs Ulutaş, Emre Tepeli & Veli Çobankara. (2022) Interleukin-1 gene (IL-1) polymorphism in patients with Behçet’s Disease, and its relationship with disease manifestations. European Journal of Inflammation 20, pages 1721727X2211166.
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Grażyna Gromadzka, Diana Wierzbicka, Tomasz Litwin & Adam Przybyłkowski. (2021) Iron metabolism is disturbed and anti-copper treatment improves but does not normalize iron metabolism in Wilson’s disease. BioMetals 34:2, pages 407-414.
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Grażyna Gromadzka, Beata Tarnacka, Anna Flaga & Agata Adamczyk. (2020) Copper Dyshomeostasis in Neurodegenerative Diseases—Therapeutic Implications. International Journal of Molecular Sciences 21:23, pages 9259.
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Grażyna Gromadzka, Diana Wierzbicka, Tomasz Litwin & Adam Przybyłkowski. (2020) Difference in iron metabolism may partly explain sex-related variability in the manifestation of Wilson’s disease. Journal of Trace Elements in Medicine and Biology 62, pages 126637.
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Anna Kluska, Maria Kulecka, Tomasz Litwin, Karolina Dziezyc, Aneta Balabas, Magdalena Piatkowska, Agnieszka Paziewska, Michalina Dabrowska, Michal Mikula, Diana Kaminska, Anna Wiernicka, Piotr Socha, Anna Czlonkowska & Jerzy Ostrowski. (2019) Whole-exome sequencing identifies novel pathogenic variants across the ATP7B gene and some modifiers of Wilson's disease phenotype . Liver International 39:1, pages 177-186.
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France Woimant, Pascal Chaine & Aurélia Poujois. 2018. Neurometabolic Hereditary Diseases of Adults. Neurometabolic Hereditary Diseases of Adults 147 168 .
Xiaoyan Wu, Peter Leegwater & Hille Fieten. (2016) Canine Models for Copper Homeostasis Disorders. International Journal of Molecular Sciences 17:2, pages 196.
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Chen Chen, Bo Shen, Jia-Jia Xiao, Rong Wu, Sarah Jane Duff Canning & Xiao-Ping Wang. (2015) Currently Clinical Views on Genetics of Wilson's Disease. Chinese Medical Journal 128:13, pages 1826-1830.
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Grażyna Gromadzka, Monika Kruszyńska, Diana Wierzbicka, Tomasz Litwin, Karolina Dzieżyc, Agata Wierzchowska-Ciok, Grzegorz Chabik & Anna Członkowska. (2015) Gene variants encoding proteins involved in antioxidant defense system and the clinical expression of Wilson disease. Liver International 35:1, pages 215-222.
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Vasiliki A. Galani, Sofia Markoula, Leandros Lazaros, Paris Ladias & Ioannis Georgiou. 2015. Genomic Elements in Health, Disease and Evolution. Genomic Elements in Health, Disease and Evolution 155 193 .
Karolina Dzie?yc, Tomasz Litwin, Grzegorz Chabik, Karolina Gramza & Anna Cz?onkowska. (2014) Families with Wilson's disease in subsequent generations: Clinical and genetic analysis. Movement Disorders 29:14, pages 1828-1832.
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Adam Przyby?kowski, Gra?yna Gromadzka & Anna Cz?onkowska. (2014) Polymorphisms of metal transporter genes DMT1 and ATP7A in Wilson's disease. Journal of Trace Elements in Medicine and Biology 28:1, pages 8-12.
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Grzegorz Chabik, Tomasz Litwin & Anna Cz?onkowska. (2013) Concordance rates of Wilson?s disease phenotype among siblings. Journal of Inherited Metabolic Disease 37:1, pages 131-135.
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Tomasz Litwin & Anna Członkowska. (2013) Choroba Wilsona – czynniki wpływające na obraz kliniczny. Neurologia i Neurochirurgia Polska 47:2, pages 161-169.
Crossref
T. Litwin, G. Gromadzka & A. Członkowska. (2012) Apolipoprotein E gene (APOE) genotype in Wilson’s disease: Impact on clinical presentation. Parkinsonism & Related Disorders 18:4, pages 367-369.
Crossref
T. Litwin, G. Gromadzka, J. Samochowiec, A. Grzywacz, A. Członkowski & A. Członkowska. 2013. JIMD Reports - Case and Research Reports, 2012/5. JIMD Reports - Case and Research Reports, 2012/5 73 80 .

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