Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Ozcakar ZB"'
Autor:
Yuksel, S, Gonul, II, Canpolat, N, Gokce, I, Ozlu, SG, Ozcakar, ZB, Ozaltin, F, Soylemezoglu, O
Background The aim of this study was to investigate the histopathological findings in kidney biopsies in children with atypical hemolytic uremic syndrome (aHUS) and to determine whether specific pathological findings in aHUS have a prognostic value.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::bb061880f0c1b6794dd760d4135210a4
Autor:
Ozdemir, G, Gulhan, B, Atayar, E, Saygili, S, Soylemezoglu, O, Ozcakar, ZB, Eroglu, FK, Candan, C, Demir, BK, Soylu, A, Yuksel, S, Alpay, H, Agbas, A, Duzova, A, Hayran, M, Ozaltin, F, Topaloglu, R
Background Alport syndrome (AS) is an inherited glomerular disease caused by mutations in COL4A3, COL4A4, or COL4A5. Associations between clinical manifestations and genotype are not yet well defined. Our study aimed to define clinical and genetic ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::7b0cf339d48fa8b58d350d919adad602
Autor:
OZCAKAR, ZB, OZALTIN, F, HAYRAN, KADİR MUTLU, KORKMAZ, E, GULHAN, B, SÖYLEMEZOĞLU, HÜSNÜ OĞUZ, BESBAS, N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10046::f8a37cdbae5edd7398a0cf7643028e44
https://avesis.gazi.edu.tr/publication/details/3b75c4cb-bb39-4d58-9114-be86023dbfc4/oai
https://avesis.gazi.edu.tr/publication/details/3b75c4cb-bb39-4d58-9114-be86023dbfc4/oai
Studies relating to first-line, early, and long-term eculizumab treatment and outcomes in children with atypical hemolytic uremic syndrome (aHUS) are scarce and unclear. The aim of this case-series study was to evaluate the outcomes of first-line, ea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::960fde15ad78c894505f0a407091a1b7
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/22873
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/22873
Urofacial syndrome (UFS) (or Ochoa syndrome) is an autosomal-recessive disease characterized by congenital urinary bladder dysfunction, associated with a significant risk of kidney failure, and an abnormal facial expression upon smiling, laughing, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2295::9c68427d582e2c74b36f82524843b75a
http://www.manchester.ac.uk/escholar/uk-ac-man-scw:262860
http://www.manchester.ac.uk/escholar/uk-ac-man-scw:262860
Familial Mediterranean fever (FMF) is an autosomal recessive disease characterized by recurrent self-limited attacks of fever and polyserositis. Reactive amyloid A amyloidosis is the most devastating complication of FMF, and amyloidosis continues to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::470fab9e1553687d899f41ed4fd86c26
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/20860
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/20860
It is well known that the serum procalcitonin (PCT) levels increase in severe bacterial infections. However, there is little information about the levels of PCT in diverse diseases except mainly the infectious diseases. The aim of this study was to i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2ba12fae35394132afaa4f0869dd7dc5
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/13684
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/13684
WOS: 000228988300032 PubMed ID: 15895911 …
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9491::0dcba902546f63db39867f5fa5d4f361
https://hdl.handle.net/20.500.12605/7824
https://hdl.handle.net/20.500.12605/7824
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