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Pediatria Polska|February 1, 1995
[Arterial hypertension as a complication of homocystinuria in a 14-year old boy]E Cichocka, J KubalskaKlinika Oczna|December 1, 1990
[Metabolic cataract among the children from the Children's Health Center]J Juszko, J Kubalska, M SzreterKlinika Oczna|June 1, 1994
[Ocular problems in children with homocystinuria]J Juszko, J Kubalska, K KanigowskaActa Anthropogenetica|January 1, 1985
Disturbances in histidine metabolism in children with speech abnormalitiesD Pieniazek, J Kubalska, E Pronicka, et al.Human Genetics|July 8, 1998
LDL-R and Apo-B-100 gene mutations in Polish familial hypercholesterolemiasB Górski, J Kubalska, M Naruszewicz, et al.European Journal of Endocrinology|November 4, 2011
Reproductive function in men affected by X-linked adrenoleukodystrophy/adrenomyeloneuropathyT J Stradomska, J Kubalska, R Janas, et al.Klinische Padiatrie|March 1, 1984
9p-syndrome: two new observationsJ Szymańska, A Gutkowska, J Kubalska, et al.Human Genetics|January 1, 1984
Prenatal diagnosis of Sanfilippo disease type BW J Kleijer, J G Huijmans, W Blom, 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.Journal of Inherited Metabolic Disease|March 27, 2009
Maternal tetrahydrobiopterin deficiency: the course of two pregnancies and follow-up of two children in a mother with 6-pyruvoyl-tetrahydropterin synthase deficiencyM Giżewska, G Hnatyszyn, L Sagan, et al.Pageof 2