Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mehmet Arda Kılınç"'
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
Simetrik periferal kangren; büyük ven tıkanıklığı olmaksızın iki ya da daha fazla bölgenin iskemisidir. Bu durum sepsisin nadir görülen ancak mortalitesi yüksek bir komplikasyonudur. Olguların yaklaşık yarısında ampütasyona gidiş
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9436::2b5f4562756079445c00a61250e86d61
https://hdl.handle.net/11454/10202
https://hdl.handle.net/11454/10202
Autor:
Zeliha Şafak Taviloğlu, Ercan Sivasli, Mehmet Almacıoğlu, Mehmet Arda Kılınç, Onur Balci, Ahmet Fatih Yılmaz, Celal Varan, Mehmet Enes Coşkun
Publikováno v:
Gaziantep Medical Journal. 18:81
With the neighboring cities, our university hospital provides service to a wide area, and in this study we aimed to expose the incidence, and distribution of the congenital anomalies of the newborns that hospitalized in the period of September 2009 a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f640de04ded161428369db472276fd3
https://doi.org/10.5455/gmj-30-2012-90
https://doi.org/10.5455/gmj-30-2012-90
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