Zobrazeno 1 - 10
of 1 651
pro vyhledávání: '"Low serum ceruloplasmin"'
Publikováno v:
Zeitschrift für Gastroenterologie.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6191cb6d731201e37d0ae11e118f3e41
https://doi.org/10.1055/s-0039-1691921
https://doi.org/10.1055/s-0039-1691921
Autor:
Sezen, Hatice1 haticesezen27@mynet.com, Savik, Emin1, Kaymaz, Ahmet1, Erkus, Musluhittin Emre2, Altiparmak, Ibrahim Halil2, Nurdağ, Abdullah3, İlter, Abdusselam4, Aksoy, Nurten1
Publikováno v:
Journal of Harran University Medical Faculty / Harran Üniversitesi Tıp Fakültesi Dergisi. 2015, Vol. 12 Issue 2, p200-205. 6p.
Autor:
Merle, Uta1 uta_merle@med.uni-heidelberg.de, Weiss, Karl Heinz1, Eisenbach, Christoph1, Tuma, Sabine1, Ferenci, Peter2, Stremmel, Wolfgang1
Publikováno v:
Annals of Gastroenterology & Hepatology. 2010, Vol. 8 Issue 87, p1-6. 6p.
Akademický článek
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Autor:
E. D’Acunto, H. Freeze, A. Di Nuzzi, Pietro Vajro, B.G. Ng, M. Maccarana, K. Zielinska, Claudia Mandato, Marco Poeta, E. Ecklund, Luca Pierri
Publikováno v:
Digestive and Liver Disease. 49:e249
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b3e71dc9573dd5a3ff34e52f655f0e2
https://doi.org/10.1016/j.dld.2017.09.021
https://doi.org/10.1016/j.dld.2017.09.021
Publikováno v:
BMC Gastroenterology, Vol 10, Iss 1, p 8 (2010)
Abstract Background Mutations in the gene ATP7B cause Wilson disease, a copper storage disorder with a high phenotypic and genetic heterogeneity. We aimed to evaluate whether 'severe' protein-truncating ATP7B mutations (SMs) are associated with low s
Externí odkaz:
https://doaj.org/article/b4db353d6a0e4185bf864d64a423c6c5
Publikováno v:
Irish medical journal. 109(1)
The first step in screening for potential Wilson disease is serum ceruloplasmin testing, whereby a level of less than 0.2g/L is suggestive of the disease. We aimed to determine what proportion of an Irish population had a low ceruloplasmin level, whe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b0eae4382dcdbf1d1d238486aea7c0a
https://pubmed.ncbi.nlm.nih.gov/26904791
https://pubmed.ncbi.nlm.nih.gov/26904791
Autor:
Poeta, M., Zielinska, K., Maccarana, M., Mandato, C., Ng, B.G., Di Nuzzi, A., D’Acunto, E., Pierri, L., Ecklund, E., Freeze, H., Vajro, P.
Publikováno v:
In Digestive and Liver Disease October 2017 49(4) Supplement:e249-e249
Autor:
SEZEN, Hatice, SAVİK, Emin, KAYMAZ, Ahmet, ERKUS, Musluhittin Emre, ALTİPARMAK, İbrahim Halil, NURDAĞ, Abdullah, İLTER, Abdusselam, AKSOY, Nurten
Publikováno v:
Volume: 12, Issue: 2 200-205
Harran Üniversitesi Tıp Fakültesi Dergisi
Harran Üniversitesi Tıp Fakültesi Dergisi
GirişDaha önceki çalışmalarda serum seruloplazmin (Cp) seviyesi ile aterosklerotik kalp hastalığı arasında ilişkibulunmuş ancak bu ilişkinin iskemi mi yoksa ateroskleroz mu kaynaklı olduğu araştırılmamıştır. Buçalışmanın amac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::ed98af7943d66d798281fb0967dec38b
https://dergipark.org.tr/tr/pub/hutfd/issue/39898/473736
https://dergipark.org.tr/tr/pub/hutfd/issue/39898/473736
Publikováno v:
BMC Gastroenterology
BMC Gastroenterology, Vol 10, Iss 1, p 8 (2010)
BMC Gastroenterology, Vol 10, Iss 1, p 8 (2010)
Background Mutations in the gene ATP7B cause Wilson disease, a copper storage disorder with a high phenotypic and genetic heterogeneity. We aimed to evaluate whether 'severe' protein-truncating ATP7B mutations (SMs) are associated with low serum ceru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d59873e4ea2d74a75b5b3287dd7d1b00
https://pubmed.ncbi.nlm.nih.gov/20082719
https://pubmed.ncbi.nlm.nih.gov/20082719