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Grzegorz Chabik

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Journal of Inherited Metabolic Disease|June 19, 2013
Concordance rates of Wilson's disease phenotype among siblingsGrzegorz Chabik, Tomasz Litwin, Anna Członkowska
Movement Disorders : Official Journal of the Movement Disorder Society|March 24, 2009
Monozygotic female twins discordant for phenotype of Wilson's diseaseAnna Członkowska, Grazyna Gromadzka, Grzegorz Chabik
Handbook of Clinical Neurology|April 24, 2017
Wilson disease: neurologic featuresAnna Członkowska, Tomasz Litwin, Grzegorz Chabik
Neurologia I Neurochirurgia Polska|July 14, 2010
Persistence with treatment in patients with Wilson diseaseWojciech Masełbas, Grzegorz Chabik, Anna Członkowska
Functional Neurology|January 5, 2016
Measurement of urinary copper excretion after 48-h d-penicillamine cessation as a compliance assessment in Wilson's diseaseKarolina Dzieżyc, Tomasz Litwin, Grzegorz Chabik, et al.
Gait & Posture|September 23, 2015
Frequencies of initial gait disturbances and falls in 100 Wilson's disease patientsKarolina Dzieżyc, Tomasz Litwin, Grzegorz Chabik, et al.
Archives of Gynecology and Obstetrics|April 22, 2009
Clinical features of hemolysis, elevated liver enzymes, and low platelet count syndrome in undiagnosed Wilson disease: report of two casesAnna Członkowska, Grażyna Gromadzka, Janine Büttner, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 21, 2014
Families with Wilson's disease in subsequent generations: clinical and genetic analysisKarolina Dzieżyc, Tomasz Litwin, Grzegorz Chabik, et al.
Journal of Hepatology|February 22, 2011
Genetic variability in the methylenetetrahydrofolate reductase gene (MTHFR) affects clinical expression of Wilson's diseaseGrażyna Gromadzka, Magdalena Rudnicka, Grzegorz Chabik, et al.
Functional Neurology|July 12, 2014
Liver cirrhosis in patients newly diagnosed with neurological phenotype of Wilson's diseaseAdam Przybyłkowski, Grażyna Gromadzka, Grzegorz Chabik, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Journal of Inherited Metabolic Disease|June 19, 2013
Concordance rates of Wilson's disease phenotype among siblingsGrzegorz Chabik, Tomasz Litwin, Anna Członkowska
Movement Disorders : Official Journal of the Movement Disorder Society|March 24, 2009
Monozygotic female twins discordant for phenotype of Wilson's diseaseAnna Członkowska, Grazyna Gromadzka, Grzegorz Chabik
Handbook of Clinical Neurology|April 24, 2017
Wilson disease: neurologic featuresAnna Członkowska, Tomasz Litwin, Grzegorz Chabik
Neurologia I Neurochirurgia Polska|July 14, 2010
Persistence with treatment in patients with Wilson diseaseWojciech Masełbas, Grzegorz Chabik, Anna Członkowska
Functional Neurology|January 5, 2016
Measurement of urinary copper excretion after 48-h d-penicillamine cessation as a compliance assessment in Wilson's diseaseKarolina Dzieżyc, Tomasz Litwin, Grzegorz Chabik, et al.
Gait & Posture|September 23, 2015
Frequencies of initial gait disturbances and falls in 100 Wilson's disease patientsKarolina Dzieżyc, Tomasz Litwin, Grzegorz Chabik, et al.
Archives of Gynecology and Obstetrics|April 22, 2009
Clinical features of hemolysis, elevated liver enzymes, and low platelet count syndrome in undiagnosed Wilson disease: report of two casesAnna Członkowska, Grażyna Gromadzka, Janine Büttner, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 21, 2014
Families with Wilson's disease in subsequent generations: clinical and genetic analysisKarolina Dzieżyc, Tomasz Litwin, Grzegorz Chabik, et al.
Journal of Hepatology|February 22, 2011
Genetic variability in the methylenetetrahydrofolate reductase gene (MTHFR) affects clinical expression of Wilson's diseaseGrażyna Gromadzka, Magdalena Rudnicka, Grzegorz Chabik, et al.
Functional Neurology|July 12, 2014
Liver cirrhosis in patients newly diagnosed with neurological phenotype of Wilson's diseaseAdam Przybyłkowski, Grażyna Gromadzka, Grzegorz Chabik, et al.
Pageof 2