Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Serim Pul"'
Autor:
Neslihan Cicek, Ceren Alavanda, Ece Bodur Demirci, Serçin Güven, Ibrahim Gökce, Nurdan Yildiz, Harika Alpay, Mehtap Sak, Pinar Ata, Özde Nisa Türkkan, Serim Pul
Publikováno v:
Volume: 34, Issue: 3 254-259
Marmara Medical Journal
Marmara Medical Journal
Objective: Classical Bartter syndrome (cBS) and Gitelman syndrome (GS) are genotypically distinct, but there is a phenotypic overlapamong these two diseases, which can complicate the accurate diagnosis without genetic analysis. This study aimed to ev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::faff3f8b302a865addf6725e2f2cdd7f
https://doi.org/10.5472/marumj.1012351
https://doi.org/10.5472/marumj.1012351
Autor:
Neslihan Cicek, Harika Alpay, Sercin Guven, Ceren Alavanda, Özde Nisa Türkkan, Serim Pul, Ece Demirci, Nurdan Yıldız, Pınar Ata, Ibrahim Gokce
Background Cubilin is one of the receptor proteins responsible for reabsorption of albumin in proximal tubules and is encoded by the CUBN gene. We aimed to evaluate clinical and genetic characterization of six patients with proteinuria who had CUBN m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ff7d4207b6ae4185f5e5025a3963e48
https://hdl.handle.net/11424/281728
https://hdl.handle.net/11424/281728
Autor:
Serçin Güven, İbrahim Gökçe, Ceren Alavanda, Neslihan Çiçek, Ece Bodur Demirci, Mehtap Sak, Serim Pul, Özde Nisa Türkkan, Nurdan Yıldız, Pınar Ata, Harika Alpay
Publikováno v:
Web of Science
Introduction. Bartter syndrome (BS) is a group of autosomal-recessive tubular disorders and it is classified into five genetic subtypes. BS can also be classified by phenotype (antenatal, classic). Patients with mutations in the same gene can present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28558ebd3f92bd7f22e117848f9bf0d4
https://hdl.handle.net/11424/282848
https://hdl.handle.net/11424/282848
Autor:
Serim Pul, İbrahim Gökçe, Ece Demirci Bodur, Serçin Güven, Neslihan Çiçek, Mehtap Sak, Özde Nisa Türkkan, Deniz Filinte, Cemile Pehlivanoğlu, Betül Sözeri, Harika Alpay
Publikováno v:
The Turkish Journal of Pediatrics. 65:330
Background. Antiphospholipid syndrome (APS), particularly the catastrophic antiphospholipid syndrome (CAPS), is one of the rare causes of thrombotic microangiopathy (TMA). CAPS is the most severe form of APS, especially when accompanied by complement
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bdac6080a74e6cbb63b4b4d17e77e04
https://doi.org/10.24953/turkjped.2022.288
https://doi.org/10.24953/turkjped.2022.288
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