Výsledky vyhledávání - "Serçin Güven"

Akademický článek

Magnesium and Anti-phosphate Treatment with Bisphosphonates for Generalised Arterial Calcification of Infancy: A Case Report

Autor: Fatma Dursun, Tülay Atasoy Öztürk, Serçin Güven, Heves Kırmızıbekmez, Gülcan Seymen Karabulut, Sevinç Kalın, Betül Sözeri

Publikováno v: JCRPE, Vol 11, Iss 3, Pp 311-318 (2019)

Generalized arterial calcification of infancy (GACI) is a rare autosomal-recessive disorder, characterized by calcification of the internal elastic lamina, fibrotic myointimal proliferation of muscular arteries and resultant arterial stenosis. Treatm

Externí odkaz: https://doaj.org/article/bf2de6bfe7c344f6a7ccac7ab57ff98f

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Akademický článek

Changes in Bacterial Resistance Patterns of Pediatric Urinary Tract Infections and Rationale for Empirical Antibiotic Therapy

Autor: İbrahim Gökçe, Neslihan Çiçek, Serçin Güven, Ülger Altuntaş, Neşe Bıyıklı, Nurdan Yıldız, Harika Alpay

Publikováno v: Balkan Medical Journal, Vol 34, Iss 5, Pp 432-435 (2017)

Background: The causative agent spectrum and resistance patterns of urinary tract infections in children are affected by many factors. Aims: To demonstrate antibiotic resistance in urinary tract infections and changing ratio in antibiotic resistance

Externí odkaz: https://doaj.org/article/4e03dccbecf8457a8d64500dbb8c5e7a

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Molecular Aspects of Distal Kidney Tubular Acidosis in Children, Its Long-Term Outcome, and Relationship with Hyperammonemia

Autor: Serçin, Güven, İbrahim, Gökçe, Ceren, Alavanda, Burcu, Öztürk Hişmi, Neslihan, Çiçek, Ece, Bodur Demirci, Mehtap, Sak, Nurdan, Yıldız, Pınar, Ata, Harika, Alpay

Publikováno v: Turkish Archives of Pediatrics. 57:432-440

Objective: We aimed to present the characteristics, genetic analysis results, long-term prognosis of our patients with distal kidney tubular acidosis, and the relationship between hyperammonemia and distal kidney tubular acidosis. Materials and Metho

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b993de48c7c0c0f565b748829581f534
https://doi.org/10.5152/turkarchpediatr.2022.21362

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Assessment of the oral health status of children with chronic kidney disease

Autor: Berkant Sezer, Remziye Kaya, Nur Kodaman Dokumacıgil, Duygu Sıddıkoğlu, Serçin Güven, Nurdan Yıldız, Harika Alpay, Betül Kargül

Publikováno v: Pediatric Nephrology. 38:269-277

There are various oral symptoms related to the disease and its management in individuals with chronic kidney disease (CKD). The aim of the study was to investigate the oral health status of children with different stages of CKD, kidney transplant rec

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a096646deffe6b9e5f38983a041f92d
https://doi.org/10.1007/s00467-022-05590-6

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Differential diagnosis of classical Bartter syndrome and Gitelman syndrome: Do we need genetic analysis?

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

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

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Phenotypic and genotypic characteristics of children with Bartter syndrome

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

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Catastrophic antiphospholipid syndrome accompanied by complement regulatory gene mutation

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

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