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1829 5
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1853 6
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1855 11
1856 10
1858 1
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1862 3
1863 1
1864 3
1865 5
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1867 3
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1878 10
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1900 10
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1913 22
1914 13
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1917 33
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1920 28
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1922 15
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1924 34
1925 36
1926 27
1927 35
1928 26
1929 17
1930 26
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1932 21
1933 30
1934 24
1935 33
1936 34
1937 23
1938 18
1939 29
1940 17
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1944 12
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149,993 results

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Page 1
Wilson's disease and other neurological copper disorders.
Bandmann O, Weiss KH, Kaler SG. Bandmann O, et al. Lancet Neurol. 2015 Jan;14(1):103-13. doi: 10.1016/S1474-4422(14)70190-5. Lancet Neurol. 2015. PMID: 25496901 Free PMC article. Review.
The copper metabolism disorder Wilson's disease was first defined in 1912. Wilson's disease can present with hepatic and neurological deficits, including dystonia and parkinsonism. ...Furthermore, Wilson's disease needs to be differentiat …
The copper metabolism disorder Wilson's disease was first defined in 1912. Wilson's disease can present with hep …
Wilson's disease: update on pathogenesis, biomarkers and treatments.
Shribman S, Poujois A, Bandmann O, Czlonkowska A, Warner TT. Shribman S, et al. J Neurol Neurosurg Psychiatry. 2021 Oct;92(10):1053-1061. doi: 10.1136/jnnp-2021-326123. Epub 2021 Aug 2. J Neurol Neurosurg Psychiatry. 2021. PMID: 34341141 Review.
Wilson's disease is an autosomal-recessive disorder of copper metabolism caused by mutations in ATP7B and associated with neurological, psychiatric, ophthalmological and hepatic manifestations. ...Finally, we cover the use of established and novel chelating agents, …
Wilson's disease is an autosomal-recessive disorder of copper metabolism caused by mutations in ATP7B and associated with neur …
A genetic study of Wilson's disease in the United Kingdom.
Coffey AJ, Durkie M, Hague S, McLay K, Emmerson J, Lo C, Klaffke S, Joyce CJ, Dhawan A, Hadzic N, Mieli-Vergani G, Kirk R, Elizabeth Allen K, Nicholl D, Wong S, Griffiths W, Smithson S, Giffin N, Taha A, Connolly S, Gillett GT, Tanner S, Bonham J, Sharrack B, Palotie A, Rattray M, Dalton A, Bandmann O. Coffey AJ, et al. Brain. 2013 May;136(Pt 5):1476-87. doi: 10.1093/brain/awt035. Epub 2013 Mar 21. Brain. 2013. PMID: 23518715 Free PMC article.
The likelihood of mutations in genes other than ATP7B causing a Wilson's disease phenotype is therefore very low. We report the first cases with Wilson's disease due to segmental uniparental isodisomy as well as three patients with three ATP7B mutation …
The likelihood of mutations in genes other than ATP7B causing a Wilson's disease phenotype is therefore very low. We report th …
EASL Clinical Practice Guidelines: Wilson's disease.
European Association for Study of Liver. European Association for Study of Liver. J Hepatol. 2012 Mar;56(3):671-85. doi: 10.1016/j.jhep.2011.11.007. J Hepatol. 2012. PMID: 22340672 Free article.
This Clinical Practice Guideline (CPG) has been developed to assist physicians and other healthcare providers in the diagnosis and management of patients with Wilson's disease. The goal is to describe a number of generally accepted approaches for diagnosis, preventi …
This Clinical Practice Guideline (CPG) has been developed to assist physicians and other healthcare providers in the diagnosis and managemen …
Wilson's disease.
Pfeiffer RF. Pfeiffer RF. Handb Clin Neurol. 2011;100:681-709. doi: 10.1016/B978-0-444-52014-2.00049-5. Handb Clin Neurol. 2011. PMID: 21496616 Review.
In the almost 100 years since Wilson's description of the illness that now bears his name, tremendous advances have been made in our understanding of this disorder. ...In this chapter, the clinical manifestations, diagnostic evaluation, and treatment approaches for …
In the almost 100 years since Wilson's description of the illness that now bears his name, tremendous advances have been made …
Wilson's disease.
Ferenci P. Ferenci P. Clin Liver Dis. 1998 Feb;2(1):31-49, v-vi. doi: 10.1016/s1089-3261(05)70362-7. Clin Liver Dis. 1998. PMID: 15560044 Review.
The Wilson's disease gene on chromosome 13 codes for a copper transporting P-type ATPase-ATP7B. ...Orthotopic liver transplantation is indicated in advanced cases with hepatic decompensation or in patients with fulminant Wilson's disease....
The Wilson's disease gene on chromosome 13 codes for a copper transporting P-type ATPase-ATP7B. ...Orthotopic liver transplant …
Wilson's disease: Food therapy out of trace elements.
Li WJ, Chen HL, Wang B, Yao L, Wang XP. Li WJ, et al. Front Cell Dev Biol. 2022 Dec 21;10:1091580. doi: 10.3389/fcell.2022.1091580. eCollection 2022. Front Cell Dev Biol. 2022. PMID: 36619859 Free PMC article. Review.
Hepatolenticular degeneration, also known as Wilson's disease (WD), is an autosomal recessive inheritance nervous disorder of copper metabolism. ...
Hepatolenticular degeneration, also known as Wilson's disease (WD), is an autosomal recessive inheritance nervous disorder of …
Neurological Wilson's Disease Signs-Hepatic Encephalopathy or Copper Toxicosis?
Jopowicz A, Tarnacka B. Jopowicz A, et al. Diagnostics (Basel). 2023 Feb 27;13(5):893. doi: 10.3390/diagnostics13050893. Diagnostics (Basel). 2023. PMID: 36900037 Free PMC article. Review.
Wilson's disease (WD) is a rare autosomal recessive (AR) disorder resulting from mutations in the ATP7B gene, which is responsible for the encryption of transmembrane copper transporting ATPase. ...While disease presentation is most often asymptomatic, it could also …
Wilson's disease (WD) is a rare autosomal recessive (AR) disorder resulting from mutations in the ATP7B gene, which is respons …
Elastography of the Liver in Wilson's Disease.
Nehring P, Szeligowska J, Przybyłkowski A. Nehring P, et al. Diagnostics (Basel). 2023 May 29;13(11):1898. doi: 10.3390/diagnostics13111898. Diagnostics (Basel). 2023. PMID: 37296749 Free PMC article. Review.
Staging of liver fibrosis is of special significance in Wilson's disease as it determines the patient's prognosis and treatment. Histopathological examination is a standard method for fibrosis assessment; however, non-invasive methods like transient elastography and …
Staging of liver fibrosis is of special significance in Wilson's disease as it determines the patient's prognosis and treatmen …
149,993 results
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