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Items: 1 to 20 of 43

1.

Author Response: Small Fiber Neuropathy and Wilson Disease.

Midena E.

Invest Ophthalmol Vis Sci. 2015 Aug;56(9):5331. doi: 10.1167/iovs.15-17504. No abstract available.

PMID:
26275130
2.

Small Fiber Neuropathy and Wilson Disease.

Gondim Fde A, Gurgel Filha JH.

Invest Ophthalmol Vis Sci. 2015 Aug;56(9):5330. doi: 10.1167/iovs.15-17241. No abstract available.

PMID:
26275129
3.

Liver: A new copper cut-off value for diagnosis of Wilson disease?

Stremmel W, Merle U.

Nat Rev Gastroenterol Hepatol. 2015 Sep;12(9):493-4. doi: 10.1038/nrgastro.2015.132. Epub 2015 Aug 11. No abstract available.

PMID:
26260373
4.

Understanding and Reducing Ceruloplasmin Overuse with a Decision Support Intervention for Liver Disease Evaluation.

Tapper EB, Sengupta N, Lai M, Horowitz G.

Am J Med. 2016 Jan;129(1):115.e17-22. doi: 10.1016/j.amjmed.2015.07.019. Epub 2015 Aug 4.

PMID:
26254122
5.

Coagulation Parameters in Wilson Disease.

Schaefer M, Weber L, Gotthardt D, Seessle J, Stremmel W, Pfeiffenberger J, Weiss KH.

J Gastrointestin Liver Dis. 2015 Jun;24(2):183-8. doi: 10.15403/jgld.2014.1121.242.wls.

6.

Influence of Liver Transplantation on Neuropsychiatric Manifestations of Wilson Disease.

Yagci MA, Tardu A, Karagul S, Ertugrul I, Ince V, Kirmizi S, Unal B, Isik B, Kayaalp C, Yilmaz S.

Transplant Proc. 2015 Jun;47(5):1469-73. doi: 10.1016/j.transproceed.2015.04.017.

PMID:
26093745
7.

Functional characterization of new mutations in Wilson disease gene (ATP7B) using the yeast model.

Papur OS, Terzioglu O, Koc A.

J Trace Elem Med Biol. 2015;31:33-6. doi: 10.1016/j.jtemb.2015.02.006. Epub 2015 Mar 5.

PMID:
26004889
8.

MRI and oxidative stress markers in neurological worsening of Wilson disease following penicillamine.

Ranjan A, Kalita J, Kumar V, Misra UK.

Neurotoxicology. 2015 Jul;49:45-9. doi: 10.1016/j.neuro.2015.05.004. Epub 2015 May 21.

PMID:
26004675
9.

Spectrum of mutations in the ATP binding domain of ATP7B gene of Wilson Disease in a regional Indian cohort.

Guggilla SR, Senagari JR, Rao PN, Madireddi S.

Gene. 2015 Sep 10;569(1):83-7. doi: 10.1016/j.gene.2015.05.031. Epub 2015 May 14.

PMID:
25982861
10.

Haemolytic anaemia as first manifestation of Wilson's disease: a report of two cases.

Santra G, Paul R, Choudhury PS, Ghosh SK, De D, Das S.

J Assoc Physicians India. 2014 Oct;62(10):55-7.

PMID:
25906525
11.

Clinical zinc deficiency as early presentation of Wilson disease.

Van Biervliet S, Küry S, De Bruyne R, Vanakker OM, Schmitt S, Vande Velde S, Blouin E, Bézieau S.

J Pediatr Gastroenterol Nutr. 2015 Apr;60(4):457-9. doi: 10.1097/MPG.0000000000000628.

PMID:
25825851
12.

Hepatic steatosis in Wilson disease--Role of copper and PNPLA3 mutations.

Stättermayer AF, Traussnigg S, Dienes HP, Aigner E, Stauber R, Lackner K, Hofer H, Stift J, Wrba F, Stadlmayr A, Datz C, Strasser M, Maieron A, Trauner M, Ferenci P.

J Hepatol. 2015 Jul;63(1):156-63. doi: 10.1016/j.jhep.2015.01.034. Epub 2015 Feb 9.

PMID:
25678388
13.

Wilson disease with thrombocytopenia (case report).

Zhvania M, Gogberashvili K, Gagoshidze M, Uberi E.

Georgian Med News. 2014 Dec;(237):61-4.

PMID:
25617103
14.

Small fiber peripheral neuropathy in Wilson disease: an in vivo documentation by corneal confocal microscopy.

Sturniolo GC, Lazzarini D, Bartolo O, Berton M, Leonardi A, Fregona IA, Parrozzani R, Midena E.

Invest Ophthalmol Vis Sci. 2015 Jan 22;56(2):1390-5. doi: 10.1167/iovs.14-15004.

PMID:
25613947
15.

Wilson disease: a matter of copper, but also of zinc.

Iorio R, Ranucci G.

J Pediatr Gastroenterol Nutr. 2015 Apr;60(4):423-4. doi: 10.1097/MPG.0000000000000725. No abstract available.

PMID:
25611032
16.

Prospective pilot study of a single daily dosage of trientine for the treatment of Wilson disease.

Ala A, Aliu E, Schilsky ML.

Dig Dis Sci. 2015 May;60(5):1433-9. doi: 10.1007/s10620-014-3495-6. Epub 2015 Jan 21.

17.

Is it necessary to re-evaluate diagnostic criteria for Wilson disease in children?

Sezer OB, Perk P, Hoşnut FÖ, Köse SK, Özcay F.

Turk J Gastroenterol. 2014 Dec;25(6):690-5. doi: 10.5152/tjg.2014.7787.

18.

Myocardial integrated ultrasonic backscatter for early detection of cardiac involvement in patients with Wilson disease.

Arat N, Kaçar S, Gölbaşı Z, Akdoğan M, Kuran S.

Turk J Gastroenterol. 2014 Dec;25(6):678-84. doi: 10.5152/tjg.2014.5949.

19.

Most frequent mutation c.3402delC (p.Ala1135GlnfsX13) among Wilson disease patients in Venezuela has a wide distribution and two old origins.

Paradisi I, De Freitas L, Arias S.

Eur J Med Genet. 2015 Feb;58(2):59-65. doi: 10.1016/j.ejmg.2014.12.007. Epub 2014 Dec 12.

PMID:
25497208
20.

Gene mutations in Wilson disease in Egyptian children: report on two novel mutations.

El-Mougy FA, Sharaf SA, Elsharkawy MM, Mandour IA, El-Essawy RA, Eldin AM, Helmy HM, Soliman DH, Selim LH, Sharafeldin HM, Mogahed EA, El-Karaksy HM.

Arab J Gastroenterol. 2014 Sep-Dec;15(3-4):114-8. doi: 10.1016/j.ajg.2014.10.005. Epub 2014 Nov 21.

PMID:
25465132
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