Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Hatice Gamze Poyrazoğlu"'
Autor:
Pembe Soylu Üstkoyuncu, Mustafa Kendirci, Songül Gökay, Fatih Kardaş, Hakan Gümüş, Hüseyin Per, Hatice Gamze Poyrazoğlu, Ayşe Kaçar Bayram, Mehmet Canpolat, Sefer Kumandaş
Publikováno v:
Türk Nöroloji Dergisi, Vol 26, Iss 3, Pp 250-252 (2020)
Argininemia is an autosomal recessive urea cycle disorder caused by the deficiency of arginase. Our first case presented with psychomotor retardation, difficulty of walking, and progressive tiptoeing. Laboratory investigations revealed mildly elevate
Externí odkaz:
https://doaj.org/article/503933fff92c43379d331ccc28772cd4
Autor:
Pembe Soylu Üstkoyuncu, Ahmet Sami Güven, Hatice Gamze Poyrazoğlu, Songül Gökay, Fatih Kardaş, Mustafa Kendirci, İkbal Gökçek, Yasemin Altuner Torun
Publikováno v:
Türk Nöroloji Dergisi, Vol 25, Iss 3, Pp 135-139 (2019)
Objective: To indicate the benefits of the screening of inherited metabolic disorders in patients with epilepsy, global developmental delay, and intellectual disability. Materials and Methods: The medical records of 1100 patients who were investigat
Externí odkaz:
https://doaj.org/article/b88f5d1e5e7140dc96910258ec15826b
Autor:
Hatice Gamze Poyrazoğlu, Serkan Kırık, Mehmet Yusuf Sarı, İhsan Esen, Zülal Aşçı Toraman, Yeşim Eroğlu
Publikováno v:
The Turkish journal of pediatrics. 64(1)
Corona virus disease 2019 (COVID-19) includes a wide range of diseases with varying pathophysiology in children and adults. Although the disease mainly affects the respiratory tract, neurological involvement is also reported in the literature. The mo
Autor:
Yasemin Altuner Torun, Fatih Kardaş, Pembe Soylu Ustkoyuncu, Ahmet Sami Güven, Songul Gokay, İkbal Gökçek, Hatice Gamze Poyrazoğlu, Mustafa Kendirci
Publikováno v:
Türk Nöroloji Dergisi, Vol 25, Iss 3, Pp 135-139 (2019)
Objective: To indicate the benefits of the screening of inherited metabolic disorders in patients with epilepsy, global developmental delay, and intellectual disability. Materials and Methods: The medical records of 1100 patients who were investigate
Autor:
Hatice Gamze Poyrazoğlu, Mustafa Kendirci, Ayşe Kaçar Bayram, Pembe Soylu Ustkoyuncu, Hakan Gümüş, Fatih Kardaş, Sefer Kumandaş, Hüseyin Per, Songul Gokay, Mehmet Canpolat
Publikováno v:
Türk Nöroloji Dergisi, Vol 26, Iss 3, Pp 250-252 (2020)
Argininemia is an autosomal recessive urea cycle disorder caused by the deficiency of arginase. Our first case presented with psychomotor retardation, difficulty of walking, and progressive tiptoeing. Laboratory investigations revealed mildly elevate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52bbc31443c7244e6e0bfa26f8614b4b
https://avesis.erciyes.edu.tr/publication/details/573e2bd6-25d9-45b7-a24d-25c08944f511/oai
https://avesis.erciyes.edu.tr/publication/details/573e2bd6-25d9-45b7-a24d-25c08944f511/oai
Publikováno v:
Neurological Sciences. 37:1663-1669
Migraine is a commonly seen neurovascular disorder during childhood. Inflammation induced by the activation of cytokines and neuropeptides is implied in its pathophysiology. There is an association between inflammation and atherosclerosis in patients
Autor:
Ali Yikilmaz, Faruk Serhatlioglu, Mehmet Canpolat, Hüseyin Per, Hakan Gümüş, Rifat Ozmen, Hatice Gamze Poyrazoğlu, Sefer Kumandaş
Publikováno v:
Erciyes Tıp Dergisi/Erciyes Medical Journal. 38:159-161
Anterior spinal artery infarction is extremely rare in children; it is caused by the hypoperfusion of the anterior spinal artery, leading to ischemia. Patients typically present with acute paraparesis or quadriparesis, depending on the level of spina
Publikováno v:
Acta neurologica Belgica. 120(4)
Migraine is a neurovascular disease characterized by inflammation of the cerebral and extra cerebral vessels and appears in the form of attacks. Although the pathophysiology of migraine is not fully known, the data obtained because of long-term studi
Autor:
Hüseyin Per, Hatice Gamze Poyrazoğlu, Hakan Gümüş, Tamer Kuyucu, Recep Saraymen, Sefer Kumandaş
Publikováno v:
Journal of Pediatric Epilepsy. :239-243
West syndrome (WS) is an epileptic syndrome of early childhood. There have been a limited numbers of studies of cerebrospinal fluid (CSF) excitatory amino acid (EAA), nitric oxide (NO), and malondialdehyde (MDA) levels, as well as plasma levels of EA
Autor:
Berthold Streubel, Ayse Betul Ergul, Alper Özcan, Hatice Gamze Poyrazoğlu, Yasemin Altuner Torun, Halid Işık, Neslihan Önenli Mungan, Serdar Ceylaner, Aslihan Kiraz, Alev Arslan
Publikováno v:
Pediatrics International. 58:241-243
Pompe disease (OMIM no 232300) is an autosomal recessive inherited metabolic disorder, caused by glycogen accumulation in the lysosome due to deficiency of the lysosomal acid 03B1-glucosidase enzyme. Here we report the case of an 8-month-old girl of