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Acta Neurologica Scandinavica|March 12, 2002
Dynamics of LDL oxidation in ischemic stroke patientsD Ryglewicz, M Rodo, M Roszczynko, et al.
Dementia and Geriatric Cognitive Disorders|March 8, 2000
Apolipoprotein E genotype and lipid and lipoprotein levels in dementiaH Wehr, T Parnowski, S Puzyński, et al.
Problemy Medycyny Wieku Rozwojowego|January 1, 1990
[Further steps in regional localization of the gene coding for human arylsulfatase B (ARSB): gene assignment to the section q11-qter of chromosome 5]E Fidziańska, T Abramowicz, B Czartoryska, et al.
Neurologia I Neurochirurgia Polska|January 1, 1996
[The alpha-fetoprotein level analysis in open neural tube defects and chromosomal aberrations in the fetus]A Ilnicka, B Pawłowska, J Czyzewska, et al.
Clinical Genetics|November 15, 2005
Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's diseaseG Gromadzka, H H-J Schmidt, J Genschel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2005
p.H1069Q mutation in ATP7B and biochemical parameters of copper metabolism and clinical manifestation of Wilson's diseaseGraznya Gromadzka, Harmut H J Schmidt, Janine Genschel, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
Familial defective apolipoprotein B-100 in a group of hypercholesterolaemic patients in Poland. Identification of a new mutation Thr3492Ile in the apolipoprotein B geneM Bednarska-Makaruk, M Bisko, M F Pulawska, et al.
Dementia and Geriatric Cognitive Disorders|April 29, 2006
Differences in risk factors for dementia with neurodegenerative traits and for vascular dementiaH Wehr, M Bednarska-Makaruk, W Łojkowska, et al.
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