Zobrazeno 1 - 10 of 253 pro vyhledávání: '"GS Salomons"'
1
Enteral inulin does not affect epithelial gene expression and cell turnover within the ileoanal pouch
Autor: GS Salomons, Jan Dekker, Hans A. Büller, H. P. Meijer, Erik Heineman, Cfm Welters, Alexandra W. C. Einerhand
Publikováno v: Diseases of the Colon & Rectum. 43:1427-1434
PURPOSE: This study evaluates the effects of enteral inulin on ileoanal pouch functioning by studying epithelial gene expression, cell turnover, and mucosal morphology. METHODS: Twenty patients with an ileoanal pouch received 24 g of inulin daily for
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::af90d89971d40856226265e5bdd79e7c
https://doi.org/10.1007/bf02236640
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5
Alexander disease - astrogliopathy considered as leukodystrophy - experience of an institution
Autor: Mierzewska H, Mierzewska-Schmidt M, Gs, Salomons, Dudzińska M, Elżbieta Szczepanik
Publikováno v: ResearcherID
Scopus-Elsevier
Europe PubMed Central
Developmental period medicine, 20(2), 110-117. Instytut Matki i Dziecka
Mierzewska, H, Mierzewska-Schmidt, M, Salomons, G S, Dudzińska, M & Szczepanik, E 2016, ' Alexander disease-astrogliopathy considered as leukodystrophy-experience of an institution ', Developmental period medicine, vol. 20, no. 2, pp. 110-117 .
Alexander Disease (ALXDRD) is an autosomal dominant leukodystrophy caused by mutation in one allele of GFAP gene, encoding glial fibrillary acidic protein (GFAP). Most cases occur due to de novo. There are three clinical subtypes of ALXDRD: infantile
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0ecc9ae9b68983f5ca337e90d5deb460
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=MEDLINE&KeyUT=MEDLINE:27442695&KeyUID=MEDLINE:27442695
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7
Mild hemolytic anemia, progressive neuromotor retardation and fatal outcome: a disorder of glycolysis, triose- phosphate isomerase deficiency
Autor: Sarper N, Zengin E, Jakobs C, Gs, Salomons, Mc Wamelink M, Markus Ralser, Kurt K, Kara B
Publikováno v: Europe PubMed Central
Turkish Journal of Pediatrics, 55(2), 198-202. Turkish Journal of Pediatrics
Sarper, N, Zengin, E, Jakobs, C A J M, Salomons, G S, Wamelink, M M C, Ralser, M, Kurt, K & Kara, B 2013, ' Mild hemolytic anemia, progressive neuromotor retardation and fatal outcome: a disorder of glycolysis, triose-phosphate isomerase deficiency ', Turkish Journal of Pediatrics, vol. 55, no. 2, pp. 198-202 .
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::487873addf724f6c433fe4edf868fe76
http://europepmc.org/abstract/med/24192681
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8
Akademický článek
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9
Akademický článek
Sulfate: a neglected (but potentially highly relevant) anion.
Autor: den Bakker E; Department of Pediatric Nephrology, Emma Childrens Hospital, Amsterdam UMC, Amsterdam, the Netherlands., Smith DEC; Department of Metabolic Diseases, Amsterdam UMC, Amsterdam, the Netherlands., Finken MJJ; Department of Pediatric Endocrinology, Emma Childrens Hospital, Amsterdam UMC, Amsterdam, the Netherlands., Wamelink MMC; Department of Metabolic Diseases, Amsterdam UMC, Amsterdam, the Netherlands., Salomons GS; Department of Metabolic Diseases, Amsterdam UMC, Amsterdam, the Netherlands.; Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam UMC, Amsterdam, the Netherlands., van de Kamp JM; Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam UMC, Amsterdam, the Netherlands.; Amsterdam Reproduction and Development, Amsterdam UMC, Amsterdam, the Netherlands.; Department of Human Genetics, Amsterdam UMC, Amsterdam, the Netherlands., Bökenkamp A; Department of Pediatric Nephrology, Emma Childrens Hospital, Amsterdam UMC, Amsterdam, the Netherlands.
Publikováno v: Essays in biochemistry [Essays Biochem] 2024 Dec 04; Vol. 68 (4), pp. 391-399.
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10
Akademický článek
Plasma triacylglycerol length and saturation level mark healthy aging groups in humans.
Autor: Li W; Amsterdam UMC Location University of Amsterdam, Laboratory Genetic Metabolic Diseases, Amsterdam, The Netherlands.; Amsterdam Gastroenterology, Endocrinology and Metabolism Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands., Schomakers BV; Amsterdam UMC Location University of Amsterdam, Laboratory Genetic Metabolic Diseases, Amsterdam, The Netherlands.; Core Facility Metabolomics, Amsterdam UMC Location University of Amsterdam, 1105 AZ, Amsterdam, The Netherlands., van Weeghel M; Amsterdam UMC Location University of Amsterdam, Laboratory Genetic Metabolic Diseases, Amsterdam, The Netherlands.; Amsterdam Gastroenterology, Endocrinology and Metabolism Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.; Core Facility Metabolomics, Amsterdam UMC Location University of Amsterdam, 1105 AZ, Amsterdam, The Netherlands., Grevendonk L; Department of Nutrition and Movement Sciences, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, 6200 MD, Maastricht, The Netherlands., Vaz FM; Amsterdam UMC Location University of Amsterdam, Laboratory Genetic Metabolic Diseases, Amsterdam, The Netherlands.; Amsterdam Gastroenterology, Endocrinology and Metabolism Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.; Core Facility Metabolomics, Amsterdam UMC Location University of Amsterdam, 1105 AZ, Amsterdam, The Netherlands., Salomons GS; Amsterdam UMC Location University of Amsterdam, Laboratory Genetic Metabolic Diseases, Amsterdam, The Netherlands.; Amsterdam Gastroenterology, Endocrinology and Metabolism Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.; Core Facility Metabolomics, Amsterdam UMC Location University of Amsterdam, 1105 AZ, Amsterdam, The Netherlands., Schrauwen P; Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands.; Institute for Clinical Diabetology, German Diabetes Center, Leibniz Institute for Diabetes Research at Heinrich Heine University Düsseldorf, Düsseldorf, Germany., Hoeks J; Department of Nutrition and Movement Sciences, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, 6200 MD, Maastricht, The Netherlands., Gao AW; Amsterdam UMC Location University of Amsterdam, Laboratory Genetic Metabolic Diseases, Amsterdam, The Netherlands.; Amsterdam Gastroenterology, Endocrinology and Metabolism Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands., Houtkooper RH; Amsterdam UMC Location University of Amsterdam, Laboratory Genetic Metabolic Diseases, Amsterdam, The Netherlands.; Amsterdam Gastroenterology, Endocrinology and Metabolism Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.; Amsterdam Cardiovascular Sciences, Amsterdam, The Netherlands., Janssens GE; Amsterdam UMC Location University of Amsterdam, Laboratory Genetic Metabolic Diseases, Amsterdam, The Netherlands. g.e.janssens@amsterdamumc.nl.; Amsterdam Gastroenterology, Endocrinology and Metabolism Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands. g.e.janssens@amsterdamumc.nl.
Publikováno v: GeroScience [Geroscience] 2024 Nov 27. Date of Electronic Publication: 2024 Nov 27.
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