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J Rujner

Publications and source records attributed to J Rujner.

38 records · Page 3Linked to original sources

[Leigh disease in a 17-year-old boy].

A boy aged 1.5 year with deficient weight and height, retardation of motor development, decreased muscle tonus, finger tremor and periodic tachypnoea without detectable respiratory system changes is presented. Gasometry demonstrated metabolic acidosis with respiratory alkalosis, high concentration of lactic acid in serum and cerebrospinal fluid, increasing metabolic acidosis after glucose load, and lack of hyperglycaemic response after alanine load, and cortical atrophy in CT. On the basis of these changes Leigh's disease was diagnosed.

Alanine↗

[Polymorphism locus Pi (alpha1-antitrypsin) of residents in the Poznan province].

Locus Pi (Pi-protease inhibitor) polymorphism in the Polish population was determined with isoelectrofocusing human blood proteins in super-thin agarose gel. There were 13 phenotypes of alpha 1-antitrypsin in the tested 631 sera collected from blood donors and inhabitants of both Poznań city and Poznań province. An incidence of locus Pi alleles in the Polish population was determined: PiM1 = 0.7464; PiM2 = 0.1656; PiM3 = 0.0570; PiS = 0.0142; PiZ = 0.015; PiVar = 0.0016. Out of rare Pi variants PiI = 0.0008 and PiR = 0.0008 were identified. The obtained results were compared with those for the European populations.

Adolescent↗