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The American Journal of Clinical Nutrition|March 1, 1991
Extremely low serum pyridoxal 5'-phosphate in children with familial hypophosphatemic ricketsR D Reynolds, R S Lorenc, E Wieczorek, et al.Endokrynologia Polska|January 1, 1992
Growth rate in children with vitamin-D-dependent rickets in relation to 1-alpha-hydroxyvitamin D3 dosageE Pronicka, E Rowińska, K Buczeń, et al.Neurologia I Neurochirurgia Polska|March 1, 1987
[Role of the parathyroid glands in the pathogenesis of intracerebral calcifications]J Kulczycki, E Pronicka, E Rowińska, et al.Neurologia I Neurochirurgia Polska|March 1, 1986
[Suspected pyruvate carboxylase deficiency in 4 children with Leigh disease]E Pronicka, H Kulczycka, J Chmielik, et al.Pediatric Radiology|January 9, 1999
Dominantly inherited isolated hyperparathyroidism: a syndromic association?K Kozlowski, A Czerminska-Kowalska, H Kulczycka, et al.Journal of Pharmaceutical and Biomedical Analysis|August 8, 2001
13C NMR spectroscopy: a convenient tool for detection of argininosuccinic aciduriaH Krawczyk, A Gryff-Keller, W Gradowska, et al.Pediatric Research|November 1, 1996
Inhibition of phosphomannose isomerase by fructose 1-phosphate: an explanation for defective N-glycosylation in hereditary fructose intoleranceJ Jaeken, M Pirard, M Adamowicz, et al.Pediatric Nephrology (Berlin, Germany)|February 1, 1997
Persistent hypercalciuria and elevated 25-hydroxyvitamin D3 in children with infantile hypercalcaemiaE Pronicka, E Rowińska, H Kulczycka, et al.The Journal of Pediatrics|June 1, 1995
Pancreatic glucagon levels in infants and children with hyperinsulinemiaE Pronicka, B Gruszczyńska, B Woźniewicz, et al.Journal of Inherited Metabolic Disease|January 26, 2006
Trial of erythropoietin treatment in a boy with glutathione synthetase deficiencyJ Sykut-Cegielska, A Jurecka, J Taybert, et al.Pageof 5