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pro vyhledávání: '"Teresa J, Stradomska"'
Autor:
Teresa J Stradomska
Publikováno v:
Pediatria Polska. 85:148-155
Peroksysomy to wielofunkcyjne organelle, które spełniają kluczową rolę w licznych procesach biochemicznych dostosowując się dynamicznie do aktualnych wymogów fizjologicznych komórki. Zaburzenie struktury peroksysomów na skutek mutacji i dys
Publikováno v:
Folia neuropathologica. 52(2)
X-linked adrenoleukodystrophy is a rare, neurodegenerative peroxisomal disorder connected with mutation in the ABCD1 gene, causing impairment of the peroxisomal β-oxidation process and in consequence, accumulation of very long-chain fatty acids (VLC
Autor:
Teresa J, Stradomska
Publikováno v:
Postepy biochemii. 57(2)
Peroxisomes, classical compartments of eucaryotic cells have significant functions in cellular metabolism, which beta-oxidation fatty acids and detoxification of H2O2 are the most important biochemical process. Defects in genes encoding for peroxisom
Publikováno v:
Postepy biochemii. 57(2)
Two previously unreported inborn errors of metabolism occur in the reversible part of the pentose phosphate pathway. Deficiency of ribose-5-phosphate isomerase has been described in one patient who suffered from a progressive leukoencephalopathy and
Autor:
Małgorzata Syczewska, Zbigniew Mielniczuk, Dorota Sobielarska, Dorota Jagiełłowicz, Danuta Dzierzanowska, Teresa J. Stradomska
Publikováno v:
Journal of medical microbiology. 59(Pt 12)
A non-invasive, non-culture-based method of determining urinary d-/l-arabinitol (d-/l-ARA) ratios was investigated as a tool for the diagnosis of invasive candidiasis in nosocomial paediatric infection cases. The study encompassed 138 children aged 4
Autor:
Justyna, Paprocka, Ewa, Jamroz, Dariusz, Adamek, Teresa J, Stradomska, Ewa, Głuszkiewicz, Urszula, Grzybowska-Chlebowczyk, Elzbieta, Marszał
Publikováno v:
Folia neuropathologica. 45(4)
Peroxisomal diseases are a heterogeneous group of genetic metabolic disorders which are caused by incorrect biogenesis of peroxisomes or a defect in activity of particular enzymes located in those organelles.D-bifunctional protein (D-BP) deficiency b
Autor:
Paprocka, J., Jamroz, E., Adamek, D., Teresa J Stradomska, Głuszkiewicz, E., Grzybowska-Chlebowczyk, U., Marszał, E.
Publikováno v:
Scopus-Elsevier
Peroxisomal diseases are a heterogeneous group of genetic metabolic disorders which are caused by incorrect biogenesis of peroxisomes or a defect in activity of particular enzymes located in those organelles. D-bifunctional protein (D-BP) deficiency
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1c78eb0218712a12c82351e94c4a8279
https://ruj.uj.edu.pl/xmlui/handle/item/156562
https://ruj.uj.edu.pl/xmlui/handle/item/156562
Autor:
Danuta Dzierzanowska, Maria Dabkowska, Bogumila Bobula-Milewska, Anna Bauer, Teresa J. Stradomska, Małgorzata Syczewska, Zbigniew Mielniczuk
Publikováno v:
Journal of clinical microbiology. 43(10)
Long-term antibiotic therapy is one of the main risk factors for mycosis. The urinary d -arabinitol/ l -arabinitol ( d -/ l -ARA) ratio (a biomarker of several Candida species) was determined by gas chromatography with an electron capture detector in
Publikováno v:
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 773(2)
The D-/L-arabinitol enantiomers ratio (a marker of disseminated candidiasis of Candida species) in urine was determined by gas chromatography (GC) in 198 healthy Polish children ranging in age from 0 to 18 years. The urine samples were dry and triflu
Autor:
Stradomska TJ; Teresa J. Stradomska, Department of Biochemistry, Radioimmunology and Experimental Medicine, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland, fax: +48 22 815 13 13, e-mail: jstradomska@op.pl, j.de.stradomska@gmail.com., Drabko K, Moszczyńska E, Tylki-Szymańska A
Publikováno v:
Folia neuropathologica [Folia Neuropathol] 2014; Vol. 52 (2), pp. 159-63.