Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Melis Köse"'
Autor:
Ayşe Ergül Bozacı, Emine Göksoy, Aysel Tekmenuray Ünal, Hatice Mutlu Albayrak, İbrahim Taş, Berat Kanar, Mehmet Nuri Özbek, Melis Köse
Publikováno v:
Journal of Pediatric Research, Vol 10, Iss 3, Pp 182-194 (2023)
Aim:Urea cycle disorders (UCD) still have poor neurological outcomes despite early diagnosis and treatment. We aimed to present the neurological outcomes of UCD patients and to determine the main simple and accessible factors affecting these outcomes
Externí odkaz:
https://doaj.org/article/e3748e19c3c44e969f25d57aa5af3721
Publikováno v:
Journal of Pediatric Research, Vol 8, Iss 2, Pp 155-160 (2021)
Aim:Screening of dyslipidemia in childhood has been controversial. While some guidelines recommend screening for dyslipidemia in children, others emphasize that there is insufficient evidence for screening for dyslipidemia in those less than 20 years
Externí odkaz:
https://doaj.org/article/30faac4c4e4c4a58a387bbf23808752b
Autor:
Ferit Kulalı, Melis Köse, Tuğçe Candan Çelik, Ezgi Yangın Ergon, Oğuz Han Kalkanlı, Rüya Çolak, Meral Yıldız, Senem Alkan Özdemir, Tülin Gökmen Yıldırım, Şebnem Çalkavur
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 9, Iss 2, Pp 143-148 (2019)
INTRODUCTION: The deficiency or absence of an enzyme or cofactor in the metabolic pathway leads to the formation or accumulation of a specific metabolite resulting in inborn errors of metabolism (IEM).The neonate who is, usually, born healthy at birt
Externí odkaz:
https://doaj.org/article/2d3cf77c07b54f45b089d09de1b20adb
Autor:
Ebru Canda, Melis Köse, Mehtap Kağnıcı, Meral Dondurmacı, Sema Kalkan Uçar, Eser Sözmen, Reşit Ertürk Levent, Mahmut Çöker
Publikováno v:
Journal of Pediatric Research, Vol 6, Iss 2, Pp 121-127 (2019)
Aim:Cardiovascular involvement is common in patients with mucopolysaccharidoses (MPS). In this study, we investigated the effects of the markers involved in vascular endothelial injury pathogenesis [transforming growth factor β- (TGF-β)], interleuk
Externí odkaz:
https://doaj.org/article/ded71b00331b4eb4900d1363c422fb05
Autor:
Ebru Canda, Melis Köse, Havva Yazıcı, Esra Er, Cenk Eraslan, Ferda Özkınay, Mahmut Çoker, Sema Kalkan Uçar, Sara Habif, Emin Karaca, Hüseyin Onay
Publikováno v:
Journal of Pediatric Research, Vol 5, Iss 1, Pp 39-43 (2018)
Aim:L-2-hydroxyglutaric aciduria (L2HGA) is a rare autosomal recessive encephalopathy caused by mutations in the L-2-hydroxyglutarate dehydrogenase gene.Materials and Methods:Here we discuss the clinical and molecular characteristics in patients with
Externí odkaz:
https://doaj.org/article/f28b0eb585b54012802d2b794144d65e
Publikováno v:
Case Reports in Pediatrics, Vol 2017 (2017)
In treatment of metabolic imbalances caused by maple syrup urine disease (MSUD), peritoneal dialysis, and hemofiltration, pharmacological treatments for elimination of toxic metabolites can be used in addition to basic dietary modifications. Therapy
Externí odkaz:
https://doaj.org/article/a62f515662ed463a875a7ca46b55fb02
Publikováno v:
Pediatric Nephrology. 37:1033-1039
Autor:
Humay MEHDİYEVA, Esra IŞIK, Melis KÖSE, Bilçağ AKGÜN, Başak DURMUŞ, Araz ALPAY, Kaan KAVAKLI, Melike Sezgin EVİM, Namık Yaşar ÖZBEK, Hüseyin ONAY, Ferda OZKINAY, Tahir ATIK
Publikováno v:
Turkiye Klinikleri Journal of Medical Sciences. 42:159-163
Publikováno v:
Pediatrics International. 63:1175-1179
BACKGROUND In parallel with the increase in the number of children with life-limiting or life-threatening diseases, the need for and right to pediatric palliative care is also increasing. This study aimed to examine the metabolic diseases, evaluate t
Publikováno v:
Journal of Pediatric Research, Vol 8, Iss 2, Pp 155-160 (2021)
Aim:Screening of dyslipidemia in childhood has been controversial. While some guidelines recommend screening for dyslipidemia in children, others emphasize that there is insufficient evidence for screening for dyslipidemia in those less than 20 years