Výsledky vyhledávání - "Belde Kasap-Demir"

Akademický článek

Known But Forgotten Disease: A Ten-year-old Scurvy Case

Autor: Özlem ÜZÜM, İnci Türkan YILMAZ, Ceyda TANRIVERDİ, Fatma Ceren SARIOĞLU, Gülberat İNCE, Belde KASAP-DEMİR, Ali KANIK

Publikováno v: Forbes Tıp Dergisi, Vol 5, Iss 1, Pp 71-75 (2024)

In this case report, the symptoms, diagnosis, and treatment process of a ten-year-old male patient with cerebral palsy diagnosed with scurvy due to vitamin C deficiency are presented. A 10-year-old male patient with a diagnosis of cerebral palsy and

Externí odkaz: https://doaj.org/article/b9de4a078ef04b50b99b8bad6fa1e950

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Akademický článek

The Effect of 'Unclassified' Blood Pressure Phenotypes on Left Ventricular Hypertrophy

Autor: Belde Kasap-Demir, Cemaliye Başaran, Tülay Demircan, Gökçen Erfidan, Özgür Özdemir-Şimşek, Seçil Arslansoyu-Çamlar, Demet Alaygut, Fatma Mutlubaş, Cem Karadeniz

Publikováno v: Turkish Archives of Pediatrics, Vol 59, Iss 1, Pp 43-48 (2024)

Objective: We aimed to evaluate the clinical significance of the “unclassified” blood pressure phenotypes on left ventricular hypertrophy in children. Materials and Methods: All children evaluated with ambulatory blood pressure monitoring in t

Externí odkaz: https://doaj.org/article/f06ca360f35d4527aa57b88c0190f3f1

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Akademický článek

Pulse Wave Analysis in Obese Children with and without Metabolic Syndrome

Autor: Cemaliye Başaran, Gökçen Erfidan, Özgür Özdemir-Şimşek, Seçil Arslansoyu-Çamlar, Demet Alaygut, Fatma Mutlubaş, Cem Karadeniz, Bumin Nuri Dündar, Belde Kasap-Demir

Publikováno v: JCRPE, Vol 15, Iss 4, Pp 397-405 (2023)

INTRODUCTION: To compare pulse wave analysis (PWA) of obese children with and without metabolic syndrome (MS) with healthy, non-obese children and to evaluate the association between PWA findings and additional risk factors present in children with M

Externí odkaz: https://doaj.org/article/e68a8ae45e9549da8ff95d78d4ad6b7c

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Akademický článek

Approaches of Pediatric Nephrologists to Hypertensive Patients in Turkey (Turkish Pediatric Hypertension Working Group Study)

Autor: Belde Kasap-Demir, Mehmet Taşdemir, Duygu Övünç-Hacıhamdioğlu, İlknur Girişgen, Hasan Dursun, Mahmut Çivilibal, Meryem Benzer, Neşe Karaaslan-Bıyıklı, Neşe Özkayın, Ferah Sönmez

Publikováno v: Turkish Journal of Nephrology, Vol 31, Iss 2, Pp 110-115 (2022)

Externí odkaz: https://doaj.org/article/545d5d63db44490da0f1e81bb485427e

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Akademický článek

Cardiovascular risk assessment in children and adolescents with congenital solitary kidneys

Autor: Belde Kasap‐Demir, Eren Soyaltın, Seçil Arslansoyu‐Çamlar, Caner Alparslan, Demet Alaygut, Önder Yavaşcan, Tülay Demircan, Fatma Mutlubaş, Cem Karadeniz

Publikováno v: The Journal of Clinical Hypertension, Vol 23, Iss 2, Pp 245-252 (2021)

Abstract Patients with solitary kidneys (SKs) are at risk of hypertension (HT) and associated end‐organ damage. The authors aimed to evaluate whether children with congenital SKs (CSKs) have higher office, ambulatory, or central blood pressure (BP)

Externí odkaz: https://doaj.org/article/85b53ed923d746058dc610ac8e7cdc58

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Akademický článek

Protracted Febrile Myalgia Associated with Fever of Unknown Origin

Autor: Özlem Üzüm, Hayrullah Manyas, Kerem Yıldız, Abbasqulu Baghırov, Belde Kasap-Demir

Publikováno v: Forbes Tıp Dergisi, Vol 1, Iss 3, Pp 101-104 (2020)

Fever of unknown origin (FUO) is considered in children as fever >38.3°C (101°F) at least once a day for 8 days and more without any apparent diagnosis. There are lots of underlying factors for fever of unknown origin and the three most common etio

Externí odkaz: https://doaj.org/article/db026a9e26244b898fe5bee82dc4efc8

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Akademický článek

New Features for Child Metrics: Further Growth References and Blood Pressure Calculations

Autor: Korcan Demir, Ergun Konakçı, Güven Özkaya, Belde Kasap Demir, Samim Özen, Murat Aydın, Feyza Darendeliler

Publikováno v: JCRPE, Vol 12, Iss 2, Pp 125-129 (2020)

Many new features have recently been incorporated to ÇEDD Çözüm/Child Metrics, an online and freely accessible scientific toolset. Various auxological assessments can now be made with data of children with genetic diseases (Prader Willi syndrome,

Externí odkaz: https://doaj.org/article/bff0e5242e09408cbfb09eb815a4195a

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