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	61.	[Principles of diagnosis and the clinical course of 8 cases of Gaucher's disease (beta-glucocerebrosidase deficiency)]. [electronic resource] by Tylki-Szymańska, A Maciejko, D Rujner, J Goryluk, B Pronicka, E Producer: 19870828 In: Pediatria polska vol. 62 Availability: No items available. Save to lists Add to cart (remove)
	62.	Epidemiology of dermatomycoses of humans in central Poland. Part IV. Onychomycosis due to dermatophytes. [electronic resource] by Lupa, S Seneczko, F Jeske, J Głowacka, A Ochecka-Szymańska, A Producer: 20000313 In: Mycoses vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	63.	Amniotic tissue transplantation as a trial of treatment in some lysosomal storage diseases. [electronic resource] by Tylki-Szymańska, A Maciejko, D Kidawa, M Jabłońska-Budaj, U Czartoryska, B Producer: 19870304 In: Journal of inherited metabolic disease vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	[Preliminary assessment of occupational exposure to Glutaraldehyde in selected endoscopic workplaces]. [electronic resource] by Małaszuk, J Andrzejak, R Przybylski, M Jurga, M Szymańska, A Leszczyszyn, J Producer: 20001222 In: Medycyna pracy vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	65.	Lipidoses in Poland. [electronic resource] by Czartoryska, B Górska, D Tylki-Szymańska, A Sawnor-Korszyńska, D Zaremba, J Producer: 19970513 In: Neurologia i neurochirurgia polska vol. 30 Suppl 2 Availability: No items available. Save to lists Add to cart (remove)
	66.	Female Hunter syndrome caused by a single mutation and familial XCI skewing: implications for other X-linked disorders. [electronic resource] by Kloska, A Jakóbkiewicz-Banecka, J Tylki-Szymańska, A Czartoryska, B Węgrzyn, G Producer: 20120615 In: Clinical genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	67.	Mucopolysaccharidosis type II (Hunter syndrome): mutation "hot spots" in the iduronate-2-sulfatase gene. [electronic resource] by Rathmann, M Bunge, S Beck, M Kresse, H Tylki-Szymanska, A Gal, A Producer: 19970114 In: American journal of human genetics vol. 59 Availability: No items available. Save to lists Add to cart (remove)
	68.	Carpal tunnel syndrome in children with mucopolysaccharidoses: needs for surgical tendons and median nerve release. [electronic resource] by Pronicka, E Tylki-Szymanska, A Kwast, O Chmielik, J Maciejko, D Cedro, A Producer: 19880602 In: Journal of mental deficiency research vol. 32 ( Pt 1) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	69.	Enzyme replacement therapy for mucopolysaccharidosis II from 3 months of age: a 3-year follow-up. [electronic resource] by Tylki-Szymanska, A Jurecka, A Zuber, Z Rozdzynska, A Marucha, J Czartoryska, B Producer: 20120302 In: Acta paediatrica (Oslo, Norway : 1992) vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	70.	[Diurnal urinary excretion of adenosine cyclic-3',5'-monophosphate as an indirect parameter in evaluating parathyroid function]. [electronic resource] by Bogoniowska, Z Klimaszewski, J Kowalski, A Tylki-Szymańska, A Wieczorek, E Pronicka, E Producer: 19831217 In: Pediatria polska vol. 58 Availability: No items available. Save to lists Add to cart (remove)
	71.	[Comparison of therapeutic results in the treatment of leukemia in children at the Institute of Pediatrics, Pomeranian Medical Academy in Szczecin and at the Department of Immunology and Hematology of the Pediatrics Clinic at the University of Rostock]. [electronic resource] by Starkiewiczowa, J Blau, H J Korycka, A Kruse, H Lacki, L Szymańska, A Producer: 19770917 In: Pediatria polska vol. 52 Availability: No items available. Save to lists Add to cart (remove)
	72.	High prevalence of I179S mutation in patients with late-onset metachromatic leukodystrophy. [electronic resource] by Lugowska, A Berger, J Tylki-Szymañska, A Czartoryska, B Löschl, B Molzer, B Producer: 20020924 In: Clinical genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	73.	Clinical, biochemical and histological analysis of seven patients with cholesteryl ester storage disease. [electronic resource] by Tylki-Szymańska, A Rujner, J Lugowska, A Sawnor-Korszyńska, D Woźniewicz, B Czarnowska, E Producer: 19980408 In: Acta paediatrica Japonica : Overseas edition vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	74.	Hyaluronidase in human somatic tissues and urine: polymorphism and the activity in diseases. [electronic resource] by Fiszer-Szafarz, B Vannier, P Lityńska, A Zou, L Czartoryska, B Tylki-Szymańska, A Producer: 19950928 In: Acta biochimica Polonica vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	75.	The impact of a ketogenic diet and liver dysfunction on serum very long-chain fatty acids levels. [electronic resource] by Stradomska, T J Bachański, M Pawłowska, J Syczewska, M Stolarczyk, A Tylki-Szymańska, A Producer: 20130903 In: Lipids vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	76.	Occurrence, distribution, and phenotype of arylsulfatase A mutations in patients with metachromatic leukodystrophy. [electronic resource] by Berger, J Löschl, B Bernheimer, H Lugowska, A Tylki-Szymanska, A Gieselmann, V Molzer, B Producer: 19970606 In: American journal of medical genetics vol. 69 Availability: No items available. Save to lists Add to cart (remove)
	77.	Outcome of type III Gaucher disease on enzyme replacement therapy: review of 55 cases. [electronic resource] by Davies, E H Erikson, A Collin-Histed, T Mengel, E Tylki-Szymanska, A Vellodi, A Producer: 20080108 In: Journal of inherited metabolic disease vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	78.	Mutations of the iduronate-2-sulfatase gene in 12 Polish patients with mucopolysaccharidosis type II (Hunter syndrome). [electronic resource] by Popowska, E Rathmann, M Tylki-Szymanska, A Bunge, S Steglich, C Schwinger, E Gal, A Producer: 19950530 In: Human mutation vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	79.	Molecular and phenotypic characteristics of metachromatic leukodystrophy patients from Poland. [electronic resource] by Ługowska, A Berger, J Tylki-Szymańska, A Löschl, B Molzer, B Zobel, M Czartoryska, B Producer: 20050921 In: Clinical genetics vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	80.	Prevalence of arylsulfatase A pseudodeficiency allele in metachromatic leukodystrophy patients from Poland. [electronic resource] by Lugowska, A Czartoryska, B Tylki-Szymańska, A Bisko, M Zimowski, J G Berger, J Molzer, B Producer: 20001004 In: European neurology vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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