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

Fiber supplementation leads to increased expression of Bax, a regulator of apoptosis, within the ileoanal pouch

Autor: Cfm Welters, GS Salomons, E. Heineman, A.W.C. Einerhand, Hans A. Büller, Jan P. Dekker, HP Meijer

Publikováno v: Gastroenterology. 114:A397

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::863031eb748d9ac2aeb2bea374bd1d19
https://doi.org/10.1016/s0016-5085(98)81608-9

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

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

Therapeutic potential of living donor liver transplantation from heterozygous carrier donors in children with propionic acidemia.

Autor: Zeng, Zhi-Gui^1,2 (AUTHOR), Zhou, Guang-Peng^1,2 (AUTHOR), Wei, Lin^1,2 (AUTHOR), Qu, Wei^1,2 (AUTHOR), Liu, Ying^1,2,3 (AUTHOR), Tan, Yu-Le^1,2 (AUTHOR), Wang, Jun^1,2 (AUTHOR), Sun, Li-Ying^1,2,3 (AUTHOR) sunxlx@outlook.com, Zhu, Zhi-Jun^1,2 (AUTHOR) zhu-zhijun@outlook.com

Publikováno v: Orphanet Journal of Rare Diseases. 2/21/2022, Vol. 17 Issue 1, p1-14. 14p.