Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ali Yıkılmaz"'
Publikováno v:
İstanbul Medical Journal, Vol 19, Iss 1, Pp 52-55 (2018)
L-2 hydroxyglutaric aciduria (L2HGA) is an inherited neurometabolic disease characterized by elevated levels of L-2 hydroxyglutaric acid in urine, plasma, and cerebrospinal fluid. The disease has a progressive clinical course presenting with ataxia,
Externí odkaz:
https://doaj.org/article/a54686e6727a4d0db1aed017db1de066
Autor:
Serpil Yaylacı, Yıldız Dallar, Yavuz Sayar, Medine Ayşin Taşar, Ülkü Tıraş, Deniz Tekin, Ağahan Ünlü, Betül Ulukol, Fatma Yücel Beyaztaş, Celal Bütün, Ünal Özüm, Bora Büken, Ferhan Kandemir, Ahmet Gökoğlu, Meda Kondolot, Ahmet Menkü, Türkan Patıroğlu, Aydın Tunç, Fatih Yağmur, Ali Yıkılmaz, Taner Akar, Ufuk Beyazova, Bülent Değirmenci, Elvan İşeri, Figen Şahin, Aysun Baransel Isır, Ayşe Gül Bilen, Resmiye Oral, Nurperi Gazioğlu, Yasemin Balcı, Mesut Eryürük, Feyza Karagöz
Publikováno v:
Eurasian Journal of Emergency Medicine, Vol 15, Iss 1, Pp 24-29 (2016)
Aim: Abusive head trauma (AHT) is the most common cause of death as the result of child abuse. A task force is planned to provide training on AHT to professionals in different disciplines on clinical presentation, diagnostic workup, and organization
Externí odkaz:
https://doaj.org/article/3d6d6150a7a644d6b56ee1b013447933
Publikováno v:
Gynecology Obstetrics & Reproductive Medicine, Vol 20, Iss 1 (2016)
We present the abnormal sonographic findings in the brain of a 26-week fetus, which increased the suspicion of isolated lissencephaly. The woman had a history of prednisolone use in early pregnancy, and conceived with copper containing intra uterine
Externí odkaz:
https://doaj.org/article/137fc7e331bb457ea0cb6c212349d0ca
Publikováno v:
Dicle Medical Journal, Vol 37, Iss 4, Pp 413-417 (2010)
Wegener granulomatosis is a rare vasculitis in childhood and is associated with morbidity and mortality in untreated cases. We reported a 10 year-old female who presented with pulmonary renal syndrome. Laboratory investigations revealed the diagnosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::be1bf0b22f2b6ab9a899831ee8cd1ad8
http://www.dicle.edu.tr/fakulte/tip/dergi/yayin/374/19.pdf
http://www.dicle.edu.tr/fakulte/tip/dergi/yayin/374/19.pdf
Publikováno v:
The Eurasian journal of medicine. 40(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8a569d8e6c024cfbf2723fca2a819818
https://pubmed.ncbi.nlm.nih.gov/25610026
https://pubmed.ncbi.nlm.nih.gov/25610026
Publikováno v:
The Eurasian journal of medicine. 41(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a7ce2ef3a0f91c9ba8ef4f9cdea4d0ba
https://pubmed.ncbi.nlm.nih.gov/25610088
https://pubmed.ncbi.nlm.nih.gov/25610088
Publikováno v:
Gorm, Vol 20, Iss 1 (2016)
We present the abnormal sonographic findings in the brain of a 26-week fetus, which increased the suspicion of isolated lissencephaly. The woman had a history of prednisolone use in early pregnancy, and conceived with copper containing intra uterine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d62ab33dbdc21cb183a0fe41803d86c7
https://avesis.erciyes.edu.tr/publication/details/b249b2cf-8bad-4a12-b148-e45544ffacfd/oai
https://avesis.erciyes.edu.tr/publication/details/b249b2cf-8bad-4a12-b148-e45544ffacfd/oai
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Congenital hypothyroidism is one of the most urgent diseases of the neonate. When diagnosed and treated at an early stage, its most important complication, mental retardation, is preventable. The signs of congenital hypothyroidism are nonspecific in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c102d10c1ccd55b6e07fc7bf73d703ef
https://pubmed.ncbi.nlm.nih.gov/21274296
https://pubmed.ncbi.nlm.nih.gov/21274296
Publikováno v:
İstanbul Kuzey Klinikleri, Vol 6, Iss 2, Pp 192-195 (2019)
Poland's syndrome is a rare congenital anomaly accompanied by the absence of the pectoralis major, and the ipsilateral upper-limb and chest wall deformities. Hypoplasia of the breast, agenesis of the ipsilateral rib cartilage, athelia, and ipsilatera
Externí odkaz:
https://doaj.org/article/3c5509ea83e84e5f83566627576f003b