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1820 3
1821 2
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1828 2
1829 5
1830 1
1837 1
1838 2
1841 5
1842 11
1843 5
1844 5
1845 2
1846 2
1849 3
1851 2
1852 2
1853 6
1854 4
1855 11
1856 10
1858 1
1859 1
1860 1
1861 2
1862 3
1863 1
1864 3
1865 5
1866 5
1867 3
1869 3
1870 3
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1872 10
1874 4
1875 2
1876 2
1877 4
1878 10
1879 11
1880 11
1881 6
1882 10
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1885 3
1886 5
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1889 12
1890 7
1891 5
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1897 10
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1899 19
1900 10
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1902 12
1903 6
1904 5
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1907 15
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1909 14
1910 13
1911 13
1912 11
1913 22
1914 13
1915 42
1916 45
1917 33
1918 26
1919 23
1920 28
1921 23
1922 15
1923 22
1924 34
1925 36
1926 27
1927 35
1928 26
1929 17
1930 26
1931 29
1932 21
1933 30
1934 24
1935 33
1936 34
1937 23
1938 18
1939 29
1940 17
1941 26
1942 28
1943 27
1944 12
1945 64
1946 200
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1950 224
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1953 256
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1955 219
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149,226 results

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Page 1
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 …
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 …
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 …
Sleep Disorders in Wilson's Disease.
Cochen De Cock V, Woimant F, Poujois A. Cochen De Cock V, et al. Curr Neurol Neurosci Rep. 2019 Nov 13;19(11):84. doi: 10.1007/s11910-019-1001-4. Curr Neurol Neurosci Rep. 2019. PMID: 31720864 Review.
PURPOSE OF REVIEW: We aimed to review the sleep disorders described in Wilson's disease (WD), focusing on their mechanisms and treatments. RECENT FINDINGS: REM sleep behavior disorder or sleepiness can be warning signs of future WD. ...
PURPOSE OF REVIEW: We aimed to review the sleep disorders described in Wilson's disease (WD), focusing on their mechanisms and …
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 …
Neurologic Wilson's disease.
Lorincz MT. Lorincz MT. Ann N Y Acad Sci. 2010 Jan;1184:173-87. doi: 10.1111/j.1749-6632.2009.05109.x. Ann N Y Acad Sci. 2010. PMID: 20146697 Free article. Review.
Despite a long history, Wilson's disease, an autosomal recessive disease caused by mutations in the ATP7B gene, remains a commonly misdiagnosed import disease. ...This review focuses on the neurologic features of Wilson's disease, its diagnosis, and tr …
Despite a long history, Wilson's disease, an autosomal recessive disease caused by mutations in the ATP7B gene, remains a comm …
Wilson's Disease: A Review for the General Pediatrician.
Capone K, Azzam RK. Capone K, et al. Pediatr Ann. 2018 Nov 1;47(11):e440-e444. doi: 10.3928/19382359-20181026-01. Pediatr Ann. 2018. PMID: 30423186 Review.
Wilson's disease, also known as hepatolenticular degeneration, is an autosomal recessive genetic disorder due to a mutation of the ATP7B gene resulting in impaired hepatic copper excretion and copper accumulation in various tissues. ...The general pediatrician may b …
Wilson's disease, also known as hepatolenticular degeneration, is an autosomal recessive genetic disorder due to a mutation of …
149,226 results
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