Zobrazeno 1 - 10
of 140
pro vyhledávání: '"ilknur Erol"'
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 41, Iss 4, Pp 695-701 (2016)
Purpose: Febrile seizures (FS) are the most common type of seizures in children.The aim of this study was to evaluate the relationship between platelet indices and FS in children. Materials and Methods: This prospective study included 40 children who
Externí odkaz:
https://doaj.org/article/525ef8e513a042dcb5bda4ce30956df1
Publikováno v:
Cukurova Medical Journal, Vol 41, Iss Supplement 1, Pp 56-59 (2016)
Kardiyak tümörler tüm yaş gruplarında çok nadir görülmesine karşın rabdomiyom çocukluk çağında en sık görülen primer kardiyak tümördür. Kardiyak rabdomiyomlar miyositlerden köken alan, çoğunlukla birden çok kitleler şeklinde
Externí odkaz:
https://doaj.org/article/a5f088f9d3dc49ea948242a29ca94153
Publikováno v:
Cukurova Medical Journal, Vol 41, Iss 2, Pp 285-290 (2016)
Purpose: Thrombosis in children is a multifactorial disorder associated with both genetic and acquired factors. Idiopathic thrombosis is a rare condition. This study aimed to examine the etiology and risk factors of thrombosis in pediatric patients f
Externí odkaz:
https://doaj.org/article/dabc95ed2e62485e964d15b0134f9e36
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 41, Iss 2, Pp 285-290 (2016)
Purpose: Thrombosis in children is a multifactorial disorder associated with both genetic and acquired factors. Idiopathic thrombosis is a rare condition. This study aimed to examine the etiology and risk factors of thrombosis in pediatric patients f
Externí odkaz:
https://doaj.org/article/ee0abed3b6f34f1ebdb942904ac935d3
Publikováno v:
Cukurova Medical Journal, Vol 40, Iss 3, Pp 627-631 (2015)
Bu yazıda akut batın nedeni ile opere olan, gastrointestinal cerrahi sonrası dönemde tiamin desteği olmaksızın, total parenteral beslenme alan ve Wernike ensefalopatisi (WE), gelişen olgu sunulmuştur. Cerrahların, çocuk nörologlarının,
Externí odkaz:
https://doaj.org/article/90177ae210bc4da58ebdb242f0ae7079
Publikováno v:
Cukurova Medical Journal, Vol 40, Iss 3, Pp 614-618 (2015)
Chanarin Dorfman Sendromu multisistemik genetik geçişli metabolik hastalık olup konjenital iktiyozis ve çeşitli hücrelerde lipid depolanması ile ilişkilidir. İktiyozisli hastalarda periferik kan yaymasında nötrofillerde lipid vakuollerinin
Externí odkaz:
https://doaj.org/article/47b7dbce30234560aca0a76f8e8c9c38
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 40, Iss 3, Pp 627-631 (2015)
We herein describe a child operated for acute abdomen who developed Wernickes encephalopathy (WE) secondary to prolonged total parenteral nutrition (TPN) that lacked vitamin B1 supplementation. The author concluded that surgeons, child neurologists,
Externí odkaz:
https://doaj.org/article/b74e305c7f794c7a85e0b4e0bedde764
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 40, Iss 3, Pp 614-618 (2015)
Chanarin Dorfman Syndrome is a multisystem inherited metabolic disorder associated with congenital ichthyosis and accumulation of lipid droplets in varios types of cells. Observation of lipid vacuoles in neutrophils (Jordan's anomaly) in peirpheral b
Externí odkaz:
https://doaj.org/article/1b15b0d578534600b718c52f32f67486
Publikováno v:
Cukurova Medical Journal, Vol 40, Iss 1, Pp 169-173 (2015)
Phelan-McDermid sendromu olarak da bilinen 22q13.3 delesyon sendromu, global gelişme geriliği, gecikmiş ve gelişmemiş konuşma, jenaralize hipotoni ve minör fiziksel anomaliler ile karekterizedir. Delesyon tipik olarak 22q13.3'ün terminal band
Externí odkaz:
https://doaj.org/article/c61c89017be0466a93ad8826a185cc20
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 40, Iss 1, Pp 169-173 (2015)
Phelan-McDermid syndrome, also known as 22q13.3 deletion syndrome, is characterized by global developmental delay, absent or delayed speech, generalized hypotonia, and minor physical anomalies. The deletion typically involves the terminal band 22q13.
Externí odkaz:
https://doaj.org/article/5f993c9a596c4a26b452f433d2f1a53b