Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Fatih KARDAŞ"'
Publikováno v:
Balkan Medical Journal, Vol 40, Iss 5, Pp 312-313 (2023)
Externí odkaz:
https://doaj.org/article/4c690d54aeed487798d90941d90fc732
Publikováno v:
The Journal of Pediatric Academy, Vol 2, Iss 3, Pp 106-110 (2021)
Background: Restless Legs Syndrome (RLS), which may be a missed diagnosis in children, is seen at an important frequency. This study’s aim was to investigate the clinical characteristics of patients with RLS and to show the effect of RLS on school
Externí odkaz:
https://doaj.org/article/03f4add7eb6a4f5ea58b513860f02010
Publikováno v:
The Journal of Pediatric Academy, Vol 2, Iss 2, Pp 59-63 (2021)
Phenylketonuria is treated by either with tetrahydrobiopterin (BH4) or with phenylalanine-restricted diet. Patients on diet group may have a tendency of consume carbohydrate-rich foods and henceforth a risk of developing obesity. In this study, the p
Externí odkaz:
https://doaj.org/article/d412b207a0ee48a1a3fb1925c3196d4d
Autor:
Pembe Soylu Üstkoyuncu, Mustafa Kendirci, Songül Gökay, Fatih Kardaş, Hakan Gümüş, Hüseyin Per, Hatice Gamze Poyrazoğlu, Ayşe Kaçar Bayram, Mehmet Canpolat, Sefer Kumandaş
Publikováno v:
Türk Nöroloji Dergisi, Vol 26, Iss 3, Pp 250-252 (2020)
Argininemia is an autosomal recessive urea cycle disorder caused by the deficiency of arginase. Our first case presented with psychomotor retardation, difficulty of walking, and progressive tiptoeing. Laboratory investigations revealed mildly elevate
Externí odkaz:
https://doaj.org/article/503933fff92c43379d331ccc28772cd4
Autor:
Pembe Soylu Üstkoyuncu, Ahmet Sami Güven, Hatice Gamze Poyrazoğlu, Songül Gökay, Fatih Kardaş, Mustafa Kendirci, İkbal Gökçek, Yasemin Altuner Torun
Publikováno v:
Türk Nöroloji Dergisi, Vol 25, Iss 3, Pp 135-139 (2019)
Objective: To indicate the benefits of the screening of inherited metabolic disorders in patients with epilepsy, global developmental delay, and intellectual disability. Materials and Methods: The medical records of 1100 patients who were investigat
Externí odkaz:
https://doaj.org/article/b88f5d1e5e7140dc96910258ec15826b
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 46, Iss 1, Pp 61-65 (2018)
In recent years, transcatheter aortic valve implantation (TAVI) has been considered a novel option for the management of surgically high-risk patients requiring aortic valve replacement. Presently described is a case of acute coronary syndrome (ACS)
Externí odkaz:
https://doaj.org/article/1fb5b7faae4443aa87f30d8b9627f26d
Publikováno v:
Balkan Medical Journal, Vol 33, Iss 3, Pp 370-372 (2016)
Background: Tyrosinemia type I is an autosomal recessively inherited metabolic disease of tyrosine metabolism due to the deficiency of fumarylacetoacetate hydrolase. Clinical manifestations include hepatic failure, cirrhosis, hepatocellular carcinoma
Externí odkaz:
https://doaj.org/article/4d0d1f177915459383c369ad25f93db9
Publikováno v:
Medicina, Vol 55, Iss 5, p 139 (2019)
Background: The Glasgow prognostic score (GPS), which is obtained from a combination of C-reactive protein (CRP) and serum albumin level, predicts poor prognoses in many cancer types. Systemic inflammation also plays an important role in pathogenesis
Externí odkaz:
https://doaj.org/article/ba9e55f2c88d494abe22634198d244f0
Autor:
Gül Demet Kaya Özçora, Elif Söbü, Mehmet Canpolat, Fatih Kardaş, Mustafa Kendirci, Hakan Gümüş, Hüseyin Per, Sefer Kumandaş
Publikováno v:
Trends in Pediatrics. 3:149-155
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a48820b6886f3f8c15f50bbf137358f0
https://doi.org/10.4274/tp.2022.13008
https://doi.org/10.4274/tp.2022.13008
Autor:
Merve KARACA, Veysel GÖK, Ümmü ALAKUŞ SARI, Mehmet Akif DÜNDAR, Firdevs AYDIN, Alper ÖZCAN, Ebru YILMAZ, Mehmet CANPOLAT, Serdar CEYLANER, Fatih KARDAŞ, Musa KARAKUKCU, Ekrem ÜNAL
Publikováno v:
Journal of Translational and Practical Medicine. 1:65-67
Triosephosphate isomerase deficiency is an autosomal recessive disorder characterized by progressive neuromuscular degeneration, seizure, dystonia, weak muscles, cardiomyopathy, hemolytic anemia, and death in early childhood. In the glycolytic pathwa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e7bdb0941db8b1a975e0da2bf98c3fa
https://doi.org/10.51271/jtpm-0020
https://doi.org/10.51271/jtpm-0020