Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Carin M. L. Van Dael"'
Autor:
Rene Scheenstra, Egbert Sieders, Willem S. Lexmond, Martin Kömhoff, Patrick F. van Rheenen, Henkjan J. Verkade, Carin M. L. Van Dael, Joanne F. Goorhuis
Publikováno v:
Liver Transplantation, 21(3), 369-380. Wiley
Liver Transplantation, 21(3), 369-380. Wiley-Blackwell
Liver Transplantation, 21(3), 369-380. Wiley-Blackwell
For more than 10 years, children at our national center for pediatric liver transplantation (LT) have been treated with Molecular Adsorbent Recirculating System (MARS) liver dialysis as a bridging therapy to high-urgency LT. Treatment was reserved fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8d0c61b61823abfbf61b9b3e3305cc8
https://doi.org/10.1002/lt.24037
https://doi.org/10.1002/lt.24037
Autor:
Carin M. L. van Dael, Arend Karrenbeld, Magdalena R. Golachowska, Edmond H. H. M. Rings, Dick Hoekstra, Marc A. Benninga, Sven C.D. van IJzendoorn, Carolien F. M. Gijsbers, Hilda M. Keuning
Publikováno v:
Journal of pediatric gastroenterology and nutrition, 54(4), 491-498. Lippincott Williams and Wilkins
Journal of Pediatric Gastroenterology and Nutrition, 54(4), 491-498. Lippincott Williams and Wilkins
Journal of Pediatric Gastroenterology and Nutrition, 54(4), 491-498. LIPPINCOTT WILLIAMS & WILKINS
Journal of Pediatric Gastroenterology and Nutrition, 54(4), 491-498. Lippincott Williams and Wilkins
Journal of Pediatric Gastroenterology and Nutrition, 54(4), 491-498. LIPPINCOTT WILLIAMS & WILKINS
Microvillus inclusion disease (MVID) is a rare congenital enteropathy associated with brush border atrophy and reduced expression of enzymes at the enterocytes' apical surface. MVID is associated with mutations in the MYO5B gene, which is expressed i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70c55c958b6bfb4d3dfd8987f953e9f5
https://pure.amc.nl/en/publications/myo5b-mutations-in-patients-with-microvillus-inclusion-disease-presenting-with-transient-renal-fanconi-syndrome(5230065f-0be9-4af0-9e3c-13ef04d8c478).html
https://pure.amc.nl/en/publications/myo5b-mutations-in-patients-with-microvillus-inclusion-disease-presenting-with-transient-renal-fanconi-syndrome(5230065f-0be9-4af0-9e3c-13ef04d8c478).html
Publikováno v:
Nephrology Dialysis Transplantation, 20(2), 472-472. Oxford University Press
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f02b1b3eb210dcc4b166a37130420464
https://research.rug.nl/en/publications/24129416-7ec7-4560-bc9b-0871d5dd250d
https://research.rug.nl/en/publications/24129416-7ec7-4560-bc9b-0871d5dd250d
Publikováno v:
Nephrology Dialysis Transplantation; Feb2005, Vol. 20 Issue 2, p472-472, 1p