Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mehmet Arda Kilinc"'
Autor:
Sanem Eren Akarcan, Neslihan Karaca, Guzide Aksu, Halil Bozkaya, Mehmet Fatih Ayik, Yasemin Ozdemir Sahan, Mehmet Arda Kilinc, Zafer Dokumcu, Cenk Eraslan, Emre Divarci, Hudaver Alper, Necil Kutukculer
Publikováno v:
Case Reports in Immunology, Vol 2017 (2017)
Chronic granulomatous disease (CGD) is a primary immune deficiency causing predisposition to infections with specific microorganisms, Aspergillus species and Staphylococcus aureus being the most common ones. A 16-year-old boy with a mutation in CYBB
Externí odkaz:
https://doaj.org/article/24d93c2176d04286a3a9f9ed8b080c6c
Publikováno v:
Journal of Pediatric Research, Vol 4, Iss 4, Pp 191-194 (2017)
Superior mesenteric artery syndrome is a rare condition in patients who have oral feeding intolerance. Due to decreased fat tissue around the duodenum, the angle between the superior mesenteric artery and duodenum also decrease. Despite normal perist
Externí odkaz:
https://doaj.org/article/2aaed4f76f944bc187d1f8b0d2fa5517
Autor:
Havva Yazıcı, Ebru Canda, Esra Er, Mehmet Arda Kılınç, Sema Kalkan Uçar, Bülent Karapınar, Mahmut Çoker
Publikováno v:
Journal of Pediatric Research, Vol 5, Iss 1, Pp 57-59 (2018)
Hereditary tyrosinemia Type I (HTI) is an autosomal recessive disorder due to a deficiency of the enzyme fumarylacetoacetate hydrolase. The liver is the primary organ that is affected and comorbidities with renal and neurologic systems and hepatocell
Externí odkaz:
https://doaj.org/article/226a842c64434368b84cfc31667e0204