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Microbios|January 1, 1990
Small, heat-stable, DNA-binding proteins from Caulobacter crescentusB Paterczyk, A Lugowska, Z KwiatkowskiActa Paediatrica Japonica : Overseas Edition|October 1, 1996
Neuraminidase deficiency presenting as a nephrosialidosis: the first case detected in PolandA Tylki-Szymanska, A Lugowska, B CzartoryskaPediatria Polska|October 1, 1995
[Thin-layer chromatography of urine oligosaccharides in diagnosis of some lysosomal storage disorders]A Lugowska, A Tylki-Szymańska, D Sawnor-KorszyńskaEuropean Neurology|August 7, 1998
Practical suggestions in diagnosing metachromatic leukodystrophy in probands and in testing family membersA T Tylki-Szymańska, B Czartoryska, A LugowskaClinical Biochemistry|June 1, 1997
Elevated sulfatide excretion in compound heterozygotes of metachromatic leukodystrophy and ASA-pseudodeficiency alleleA Lugowska, A Tylki-Szymańska, J Berger, et al.Clinical Genetics|November 1, 1996
Late juvenile metachromatic leukodystrophy (MLD) in three patients with a similar clinical course and identical mutation on one alleleA Tylki-Szymanska, J Berger, B Löschl, et al.European Neurology|June 16, 2005
Assessment of relations between clinical outcome of ischemic stroke and activity of inflammatory processes in the acute phase based on examination of selected parametersW Palasik, U Fiszer, W Lechowicz, et al.Gene|July 4, 2013
Late onset GM2 gangliosidosis mimicking spinal muscular atrophyZ Jamrozik, A Lugowska, M Gołębiowski, et al.Acta Paediatrica Japonica : Overseas Edition|February 3, 1998
Clinical, biochemical and histological analysis of seven patients with cholesteryl ester storage diseaseA Tylki-Szymańska, J Rujner, A Lugowska, et al.American Journal of Medical Genetics|March 31, 1997
Occurrence, distribution, and phenotype of arylsulfatase A mutations in patients with metachromatic leukodystrophyJ Berger, B Löschl, H Bernheimer, et al.Pageof 2