Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Akif Şirikçi"'
Publikováno v:
Sakarya Tıp Dergisi, Vol 6, Iss 2, Pp 0-0 (2016)
Amaç: Karotis arter stenoz ve oklüzyonlarında altın standart olarak kabul edilen dijital subtraksiyon anjiografiye (DSA) alternatif olabilecek noninvaziv radyolojik modalitelerin etkinliğinin değerlendirilmesi amaçlanmıştır.Yöntem: Renkli
Externí odkaz:
https://doaj.org/article/727b437869884d0ba51aa2b1e4931306
Publikováno v:
Journal of Pediatric Neurology. 17:085-088
Cockayne syndrome is a rare autosomal recessive, neurodegenerative disorder characterized by a broad spectrum of clinical symptoms. Herein, we will describe a patient diagnosed with Cockayne syndrome by genetic testing who was also determined to be h
Publikováno v:
Türk Beyin Damar Hastalıkları Dergisi, Vol 22, Iss 3, Pp 129-132 (2016)
Spinal arteriovenous fistulas (AVF), are rarely seen clinical pathology, have serious morbidity in cases without treatment although spinal AVF are the most common types of spinal arteriovenous malformation. Fifty years old male patient suffered from
Autor:
Akif Şirikçi, Sedat Isikay
Publikováno v:
Journal of Pediatric Neurosciences
Guillain-Barré syndrome (GBS) is an acute inflammatory polyneuropathy. In this report, we present a 3-year-old girl diagnosed with cortical and subcortical hemorrhage during the course of GBS who was treated with intravenous immunoglobulin. To the b
Publikováno v:
Türk Beyin Damar Hastalıkları Dergisi, Vol 20, Iss 3, Pp 106-111 (2014)
Primary central nervous system vasculitis (PCNV) is limited with central nervous system and rare vasculitis that mostly seen in middle-aged men. PCNV vasculitis is usually presented that headache, dementia, stroke and multifocal common neurological s
Publikováno v:
Dicle Medical Journal, Vol 38, Iss 2, Pp 164-169 (2011)
The aim of this study was to investigate the effect of Transarterial Chemoembolization (TAKE) on tumor response survival in patients with hepatocellular carcinoma (HCC) between January 2002 and December 2008.Materials and methods: In 33 unresectable
Autor:
Akif Şirikçi, Sedat Isikay
Publikováno v:
Journal of Pediatric Neurosciences
Muscular dystrophy-dystroglycanopathy is a heterogeneous group of inherited muscular dystrophies caused by glycosylation defects associated with different mutations. The main finding of the disease is disruption of the binding of cellular alpha-dystr