Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Meral Dondurmaci"'
Publikováno v:
Journal of Pediatric Research, Vol 5, Iss 1, Pp 17-21 (2018)
WOS: 000436882600005
Aim: Recently dried blood spot (DBS) samples have been recommended as a screening test for Lysosomal Storage diseases. Although DBS samples have many advantages including non-invasiveness, cost and transportation, usage of t
Aim: Recently dried blood spot (DBS) samples have been recommended as a screening test for Lysosomal Storage diseases. Although DBS samples have many advantages including non-invasiveness, cost and transportation, usage of t
Autor:
Sema Kalkan Uçar, Meral Dondurmaci, Eser Yıldırım Sözmen, Reşit Ertürk Levent, Mahmut Çoker, Ebru Canda, Melis Köse, Mehtap Kagnici
Publikováno v:
Journal of Pediatric Research, Vol 6, Iss 2, Pp 121-127 (2019)
Aim: Cardiovascular involvement is common in patients with mucopolysaccharidoses (MPS). In this study, we investigated the effects of the markers involved in vascular endothelial injury pathogenesis [transforming growth factor ?- (TGF-?)], interleuki
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a81f54b81f2ad4eed51758bee2517b5a
https://hdl.handle.net/11454/67000
https://hdl.handle.net/11454/67000
Autor:
Ebru Canda, Eser Yıldırım Sözmen, Meral Dondurmaci, Melis Köse, Ferhan Girgin Sagin, Mahmut Çoker, Sema Kalkan Uçar
Publikováno v:
Journal of Clinical and Analytical Medicine (2018)
WOS: 000426502700014
Aim: Gaucher disease is an autosomal recessive lysosomal storage disease caused by insufficient glucocerebrosidase activity resulting in accumulation of glucosylceramide, particularly in macrophages. Multiple myeloma and B c
Aim: Gaucher disease is an autosomal recessive lysosomal storage disease caused by insufficient glucocerebrosidase activity resulting in accumulation of glucosylceramide, particularly in macrophages. Multiple myeloma and B c
Publikováno v:
Molecular Genetics and Metabolism. 120:S126
Publikováno v:
Molecular Genetics and Metabolism. 114:S110
Autor:
Ebru Canda, Melis Köse, Mehtap Kağnıcı, Meral Dondurmacı, Sema Kalkan Uçar, Eser Sözmen, Reşit Ertürk Levent, Mahmut Çöker
Publikováno v:
Journal of Pediatric Research, Vol 6, Iss 2, Pp 121-127 (2019)
Aim:Cardiovascular involvement is common in patients with mucopolysaccharidoses (MPS). In this study, we investigated the effects of the markers involved in vascular endothelial injury pathogenesis [transforming growth factor β- (TGF-β)], interleuk
Externí odkaz:
https://doaj.org/article/ded71b00331b4eb4900d1363c422fb05
Publikováno v:
Journal of Pediatric Research, Vol 5, Iss 1, Pp 17-21 (2018)
Aim:Recently dried blood spot (DBS) samples have been recommended as a screening test for Lysosomal Storage diseases. Although DBS samples have many advantages including non-invasiveness, cost and transportation, usage of these samples is limited by
Externí odkaz:
https://doaj.org/article/3c7c1d2e85bb459ab93b8500084022c4