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Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|August 1, 1986
The behavior of hepatic phosphorylase b kinase, phosphorylase a and b after administration of glucagon to patients with glycogen storage disease type VIaD Pieniazek, E Pronicka, J PawłowskaNeurologia I Neurochirurgia Polska|March 1, 1989
[Idiopathic juvenile osteoporosis with the symptoms suggesting nervous system damage]B Badurska, B Ryniewicz, E Pronicka, et al.Materia Medica Polona. Polish Journal of Medicine and Pharmacy|July 1, 1991
A case of vitamin B12--independent methylmalonic aciduriaB Gruszczyńska, Z Mielniczuk, B Katyńska, et al.Klinische Padiatrie|July 1, 1981
Three cases of beta-galactosidase deficiencyE Pronicka, A Tylki, B Czartoryska, et al.Klinische Padiatrie|July 1, 1979
The child with chromosome ring 15L Wiśniewski, E Pronicka, H Lech, et al.Klinische Padiatrie|March 1, 1991
Primary hyperparathyroidism in infants. Diagnostic and therapeutic difficultiesH Kulczycka, W Kamiński, B Woźniewicz, et al.Acta Anthropogenetica|January 1, 1985
Disturbances in histidine metabolism in children with speech abnormalitiesD Pieniazek, J Kubalska, E Pronicka, et al.Journal of Neurology|January 1, 1988
Abolished phosphaturic response to parathormone in adult patients with Fahr disease and its restoration after propranolol administrationE Pronicka, J Kulczycki, E Rowińska, et al.Materia Medica Polona. Polish Journal of Medicine and Pharmacy|October 1, 1991
A case of organic aciduria--suspected 3-hydroxy-3-methylglutaric aciduriaH Kulczycka, Z Mielniczuk, H Kamińska, et al.Materia Medica Polona. Polish Journal of Medicine and Pharmacy|July 1, 1991
Congenital lactic acidosis in children--differential diagnosis in 44 casesE Pronicka, B Gruszczyńska, B Badurska, et al.Pageof 5