Results 151 to 160 of about 288,978 (228)

Case Report: MRI Diagnosis of Wilson's Disease in a 3-Year-Old Dalmatian. [PDF]

Vet Radiol Ultrasound
Durant N, Paek M, Mai W.
europepmc   +1 more source

Usefulness of the Leipzig Score in the Diagnosis of Wilson's Disease - A Diagnostically Challenging Case Report. [PDF]

Int Med Case Rep J
Basan NM, Sheikh Hassan M, Gökhan Z, Nur Alper S, Yaşar SŞ, Gür T, Köksal A.   +6 more
europepmc   +1 more source

Sixty years of the first studies by Horácio Martins Canelas on Wilson's disease. [PDF]

Arq Neuropsiquiatr
Barbosa ER, Parmera JB, Cury RG, Cançado ELR, Bonilha PÁAM, Teive HAG.   +5 more
europepmc   +1 more source

A clinical study showing the expression characteristics of cuproptosis markers in cases with Wilson disease. [PDF]

Medicine (Baltimore)
Tao Z, Kang S, Liu J, Wang R, Zhou J, Yang W, Wang M.   +6 more
europepmc   +1 more source

Endoscopic ultrasonography-guided cyanoacrylate injection versus endoscopic cyanoacrylate injection for treating isolated gastric varices type 1 bleeding with spontaneous shunts: a randomized controlled trial. [PDF]

Therap Adv Gastroenterol
Li J, Kuai Y, Mei X, Wang Z, Zeng Z, He Y, Kong D.   +6 more
europepmc   +1 more source

A rare presentation of Wilson disease with normal levels of serum ceruloplasmin and copper and MODY: A case report. [PDF]

Medicine (Baltimore)
Han M, Yang Z.
europepmc   +1 more source

Analysis of risk factors for fatty liver disease in children with Wilson's disease. [PDF]

Eur J Gastroenterol Hepatol
Jia SP, Wang MX, Tao Z, Gao YN, Yu GR, Yang WM.   +5 more
europepmc   +1 more source

Spectrum of Pathogenic Variants of the ATP7B Gene and Genotype-Phenotype Correlation in Eastern Eurasian Patient Cohorts with Wilson's Disease. [PDF]

Biomedicines
Garbuz M, Ovchinnikova E, Ovchinnikova A, Vinokurova V, Aristarkhova Y, Kuziakova O, Mashurova M, Kumeiko V.   +7 more
europepmc   +1 more source

Hepatolenticular Degeneration

Definitions, 2013
A rare autosomal recessive inherited disorder caused by mutations in the ATP7B gene. It is characterized by copper accumulation in the tissues, particularly brain and liver. It results in liver failure, neurologic, and psychotic manifestations.
Ashutosh J Barve
openaire   +2 more sources