List of works - Grzegorz Chabik

Clinical features of hemolysis, elevated liver enzymes, and low platelet count syndrome in undiagnosed Wilson disease: report of two cases.

scientific article published on 19 April 2009

Concordance rates of Wilson's disease phenotype among siblings.

scientific article published on 18 June 2013

Early neurological worsening in patients with Wilson's disease.

scientific article published on 7 June 2015

Erratum to: Concordance rates of Wilson’s disease phenotype among siblings.

scientific article published on 5 March 2014

Erratum to: Treatment with d-penicillamine or zinc sulphate affects copper metabolism and improves but not normalizes antioxidant capacity parameters in Wilson disease.

scientific article published on 21 January 2014

Families with Wilson's disease in subsequent generations: clinical and genetic analysis

scientific article published on 18 October 2014

Frequencies of initial gait disturbances and falls in 100 Wilson's disease patients.

scientific article published on 14 September 2015

Gene variants encoding proteins involved in antioxidant defense system and the clinical expression of Wilson disease

scientific article published on 07 March 2014

Genetic variability in the methylenetetrahydrofolate reductase gene (MTHFR) affects clinical expression of Wilson's disease

scientific article published on 18 February 2011

Liver cirrhosis in patients newly diagnosed with neurological phenotype of Wilson's disease

scientific article

Measurement of urinary copper excretion after 48-h d-penicillamine cessation as a compliance assessment in Wilson's disease

scientific article published on October 2015

Monozygotic female twins discordant for phenotype of Wilson's disease

scientific article published in May 2009

Persistence with treatment in patients with Wilson disease

scientific article

Treatment with D-penicillamine or zinc sulphate affects copper metabolism and improves but not normalizes antioxidant capacity parameters in Wilson disease

scientific article published on 25 December 2013

Wilson disease: neurologic features.

scientific article published in January 2017

Wilson's disease - a case report

scientific article

p.H1069Q mutation in ATP7B and biochemical parameters of copper metabolism and clinical manifestation of Wilson's disease.

scientific article published in February 2006

List of works by Grzegorz Chabik

Clinical features of hemolysis, elevated liver enzymes, and low platelet count syndrome in undiagnosed Wilson disease: report of two cases.

Concordance rates of Wilson's disease phenotype among siblings.

Early neurological worsening in patients with Wilson's disease.

Erratum to: Concordance rates of Wilson’s disease phenotype among siblings.

Erratum to: Treatment with d-penicillamine or zinc sulphate affects copper metabolism and improves but not normalizes antioxidant capacity parameters in Wilson disease.

Families with Wilson's disease in subsequent generations: clinical and genetic analysis

Frequencies of initial gait disturbances and falls in 100 Wilson's disease patients.

Gene variants encoding proteins involved in antioxidant defense system and the clinical expression of Wilson disease

Genetic variability in the methylenetetrahydrofolate reductase gene (MTHFR) affects clinical expression of Wilson's disease

Liver cirrhosis in patients newly diagnosed with neurological phenotype of Wilson's disease

Measurement of urinary copper excretion after 48-h d-penicillamine cessation as a compliance assessment in Wilson's disease

Monozygotic female twins discordant for phenotype of Wilson's disease

Persistence with treatment in patients with Wilson disease

Treatment with D-penicillamine or zinc sulphate affects copper metabolism and improves but not normalizes antioxidant capacity parameters in Wilson disease

Wilson disease: neurologic features.

Wilson's disease - a case report

p.H1069Q mutation in ATP7B and biochemical parameters of copper metabolism and clinical manifestation of Wilson's disease.