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H Kulczycka

Showing results (1-10 of 8) with videos related to

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Klinische Padiatrie|March 1, 1991
Primary hyperparathyroidism in infants. Diagnostic and therapeutic difficultiesH Kulczycka, W Kamiński, B Woźniewicz, et al.
Wiadomosci Lekarskie (Warsaw, Poland : 1960)|September 1, 1990
[Leigh disease in a 17-year-old boy]J Rujner, W T Chruściel, H Kulczycka, 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.
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.
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.
Acta Anthropogenetica|January 1, 1985
A case of Menkes disease cell culture examination and elastic cartilage electronmicroscopyH Kulczycka, M Rodo, E Czarnowska, 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.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Klinische Padiatrie|March 1, 1991
Primary hyperparathyroidism in infants. Diagnostic and therapeutic difficultiesH Kulczycka, W Kamiński, B Woźniewicz, et al.
Wiadomosci Lekarskie (Warsaw, Poland : 1960)|September 1, 1990
[Leigh disease in a 17-year-old boy]J Rujner, W T Chruściel, H Kulczycka, 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.
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.
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.
Acta Anthropogenetica|January 1, 1985
A case of Menkes disease cell culture examination and elastic cartilage electronmicroscopyH Kulczycka, M Rodo, E Czarnowska, 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.
Pageof 1