Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Heybet, Tüzün"'
Autor:
Belma Haliloglu, Avni Kaya, Mehmet Nuri Ozbek, Heybet Tüzün, Sarah E. Flanagan, Muhittin Çelik, Sian Ellard
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Sirolimus has been reported to be effective in the treatment of the diffuse form of congenital hyperinsulinism (CHI), unresponsive to diazoxide and octreotide, without causing severe side effects. Two newborns with CHI due to homozygous ABCC8 gene mu
Autor:
Merve Emecan, Muhittin Çelik, Mehmet Şah İpek, Heybet Tüzün, Osman Akdeniz, Mücahit Fidan, Fatma Tuba Eminoğlu, Nezir Ozgun
Publikováno v:
The Turkish journal of pediatrics. 60(5)
Celik M, Ozgun N, Akdeniz O, Fidan M, Tuzun H, Ipek MS, Emecan M, Eminoglu FT. Folate deficiency in patients with classical galactosemia: A novel finding that needs to be considered for dietary treatments. Turk J Pediatr 2018; 60: 540-546. The object
Publikováno v:
Türk Pediatri Arşivi. 50:158-162
In this study, it was aimed to determine the problems of the neonates who were diagnosed with congenital heart disease requiring early intervention in our hospital.The files of the newborn babies with congenital heart disease requiring early interven
Publikováno v:
Iranian Journal of Pediatrics. 28
Objectives: To analyze the clinical and laboratory data of neonates diagnosed with Zellweger syndrome and to estimate the incidence of the syndrome. Methods: The databases of four institutions that admitted newborns diagnosed with Zellweger syndrome
Autor:
Riza Taner Baran, Melek Akar, Tijen Tanyalçın, Mehmet Nuri Ozbek, Heybet Tüzün, Bedri Aldudak, Çiğdem Seher Kasapkara
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 28
Biotinidase deficiency is an autosomal recessive inborn error of biotin metabolism. Children with biotinidase deficiency cannot cleave biocytin and, therefore, cannot recycle biotin. Untreated individuals become secondarily biotin deficient, which in
Autor:
Melek, Akar, Bedri, Aldudak, Ciğdem Seher, Kasapkara, Heybet, Tüzün, Sertaç, Hanedan Onan, Berat, Kanar, Veysiye Hülya, Uzel
Publikováno v:
Anadolu kardiyoloji dergisi : AKD = the Anatolian journal of cardiology. 14(1)
Autor:
Veysiye Hülya Uzel, Melek Akar, Heybet Tüzün, Sertaç Hanedan Onan, Berat Kanar, Çiğdem Seher Kasapkara, Bedri Aldudak
Publikováno v:
Anadolu Kardiyoloji Dergisi/The Anatolian Journal of Cardiology.
Autor:
Melek Akar, Zeynep Nagehan Yürük Yıldırım, Mehmet Nuri Ozbek, Çiğdem Seher Kasapkara, Berat Kanar, Heybet Tüzün
Publikováno v:
Renal failure. 36(3)
Neonatal-onset propionic acidemia (PA), the most common form, is characterized by poor feeding, vomiting, and somnolence in the first days of life in a previously healthy infant, followed by lethargy, seizures, and can progress to coma if not identif
Autor:
Berat Kanar, Mehmet Nuri Ozbek, Heybet Tüzün, Melek Akar, Çiğdem Seher Kasapkara, Bedri Aldudak
Publikováno v:
Renal Failure. 36:951-952
Haloperidol is commonly used in the treatment of psychiatric disorders. Data from animal experiments indicate haloperidol is not teratogenic, but is embryotoxic in high doses. For the first time, we report a neonate with transient nephrogenic diabete
Autor:
Hussain Parappil, Ugur Dilmen, Khalid Hassan, Melek Akar, Mehmet Yekta Oncel, Abdurrahman Evli, Moghis Rahman, Rohana Jaafar, Mohammad Tagin, Sajjad Ur Rahman, Mohammed Khashaba, Fuat Emre Canpolat, Lucy Chai, Zekai Tahir, Lai Yin Key, Anis Siham, Mohammed Rijims, Jasim Anabrees, Aiman Rahmani, Lina Haboub, Heybet Tüzün, Islam Ayman Noor, See Lum
Publikováno v:
Journal of Clinical Neonatology. 4:158
Background: Therapeutic hypothermia provides up to 30% neuroprotection in moderate to severe hypoxic ischemic encephalopathy (HIE). Additional neuroprotection may be achieved by using concomitant pharmacologic neuroprotective agents. Aim: The aim was