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Journal of Mental Deficiency Research|February 1, 1988
Carpal tunnel syndrome in children with mucopolysaccharidoses: needs for surgical tendons and median nerve releaseE Pronicka, A Tylki-Szymanska, O Kwast, et al.Acta Anthropogenetica|January 1, 1985
A case of Menkes disease cell culture examination and elastic cartilage electronmicroscopyH Kulczycka, M Rodo, E Czarnowska, et al.Klinische Padiatrie|April 29, 2005
[Lectin-reactive alpha-fetoprotein in tyrosinaemia type I]U Baumann, V Duhme, I Knerr, et al.Journal of Applied Genetics|October 18, 2003
X-linked hypophosphatemia in Polish patients. 1. Mutations in the PHEX geneE Popowska, E Pronicka, A Sułek, et al.Journal of Applied Genetics|October 18, 2003
SURF1 gene mutations in Polish patients with COX-deficient Leigh syndromeD Piekutowska-Abramczuk, E Popowska, E Pronicka, et al.Materia Medica Polona. Polish Journal of Medicine and Pharmacy|April 1, 1991
Urinary succinylacetone presence and delta-aminolaevulinic acid excretion in patients with type I tyrosinaemia during treatmentE Pronicka, Z Mielniczuk, E Rowińska, et al.Materia Medica Polona. Polish Journal of Medicine and Pharmacy|April 1, 1990
The surgical approach to hyperinsulinism and hypoglycemia in childrenW Kamiński, A Cedro, E Pronicka, et al.Journal of Inherited Metabolic Disease|January 24, 2002
Compulsory hyperventilation and hypocapnia of patients with Leigh syndrome associated with SURF1 gene mutations as a cause of low serum bicarbonatesE Pronicka, D H Piekutowska-Abramczuk, E Popowska, et al.Journal of Inherited Metabolic Disease|November 20, 2008
Hypoxanthine-guanine phosphoribosylotransferase deficiency--the spectrum of Polish mutationsA Jurecka, E Popowska, A Tylki-Szymanska, et al.Biochemical and Biophysical Research Communications|May 9, 2001
Abnormal calcium homeostasis in fibroblasts from patients with Leigh diseaseM Wasniewska, E Karczmarewicz, M Pronicki, et al.Pageof 5