Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Mesut Güngör"'
Autor:
Bülent Kara, Filiz Mine Çizmecioğlu Jones, Emek Uyur Yalçın, Hülya Maraş Genç, Bengü Altınordu, Mesut Güngör
Publikováno v:
Journal of Contemporary Medicine, Vol 13, Iss 1, Pp 146-152 (2023)
Background: We aimed to investigate the short-term effects of adrenocorticotropic hormone (ACTH) treatment on the adrenal pathway and bone metabolism in patients with epileptic encephalopathy. Methods: Two groups with 16 patients and 16 controls were
Externí odkaz:
https://doaj.org/article/15b9cdd3b8af4733a57df157472cb2f9
Publikováno v:
Genel Tıp Dergisi, Vol 32, Iss 6, Pp 704-707 (2022)
Juvenile absence epilepsy is an epileptic syndrome that usually begins between the ages of 9-13 and is classified in the group of genetic generalized epilepsies, in which absence seizures are seen mainly but may also be accompanied by motor seizures
Externí odkaz:
https://doaj.org/article/575a11c78395474a942bf3672c67f17e
Autor:
Hafize Emine Sönmez, Merve Savaş, Bülbül Aliyeva, Adnan Deniz, Mesut Güngör, Yonca Anık, Bülent Kara
Publikováno v:
Pediatric Neurology. 144:72-77
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08651f676bddbf23fc3c11018b8b088f
https://doi.org/10.1016/j.pediatrneurol.2023.04.008
https://doi.org/10.1016/j.pediatrneurol.2023.04.008
Autor:
Mesut GÜNGÖR, Bengü ALTINORDU, Hülya MARAŞ GENÇ, Emek UYUR YALÇIN, Filiz Mine ÇİZMECİOĞLU JONES, Bülent KARA
Publikováno v:
Journal of Contemporary Medicine. 13:146-152
Background: We aimed to investigate the short-term effects of adrenocorticotropic hormone (ACTH) treatment on the adrenal pathway and bone metabolism in patients with epileptic encephalopathy. Methods: Two groups with 16 patients and 16 controls were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef4b310c0991ad6a58a75d616ba396c3
https://doi.org/10.16899/jcm.1222558
https://doi.org/10.16899/jcm.1222558
Publikováno v:
International Journal of Rheumatic Diseases. 25:617-625
Juvenile dermatomyositis (JDM) is the most common subtype of idiopathic inflammatory myopathies in childhood. Gottron's papules, shawl sign, periorbital heliotrope rash, and periungual telengiectasis are characteristic skin findings of the disease. B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dc30ab273436243e7222eb8fca3963e
https://doi.org/10.1111/1756-185x.14311
https://doi.org/10.1111/1756-185x.14311
Autor:
Mesut Güngör, Merve Öztürk, Adnan Deniz, Defne Alikılıç, Ömer Karaca, Yonca Anık, Bülent Kara
Publikováno v:
Journal of Pediatric Neurology.
Autoimmune encephalopathy (AE) is a group of diseases with subacute onset, that represents a wide clinical spectrum, manifested by complex neuropsychiatric symptoms and signs. In this study, the data of 27 patients diagnosed and followed up in our cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8da5d6b960e2c4917935a1ac7429b68d
https://doi.org/10.1055/s-0043-1761485
https://doi.org/10.1055/s-0043-1761485
Publikováno v:
Genel Tıp Dergisi.
Juvenile absence epilepsy is an epileptic syndrome that usually begins between the ages of 9-13 and is classified in the group of genetic generalized epilepsies, in which absence seizures are seen mainly but may also be accompanied by motor seizures
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69d030e9619d3b559f8c0b4919fb2f32
https://doi.org/10.54005/geneltip.1190790
https://doi.org/10.54005/geneltip.1190790
Publikováno v:
Journal of Pediatric Neurology. 20:327-329
Reversible splenial lesion syndrome (RESLES) is a transient lesion in the splenium of the corpus callosum. Etiology includes infections, malignancies, drugs, metabolic disorders, trauma, etc. We reported radiological features of a child with RESLES a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b85f65d4ab6fbc3e3d930baa92c8497
https://doi.org/10.1055/s-0042-1748676
https://doi.org/10.1055/s-0042-1748676
Publikováno v:
Neuropediatrics. 53:140-142
Congenital CD59 deficiency is an autosomal recessive disease characterized by mild-to-moderate chronic intravascular hemolysis, relapsing demyelinating peripheral neuropathies, and recurrent ischemic central nervous system strokes. We report a 2-year
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48994ca19e936ff9ce2af9578240e8e1
https://doi.org/10.1055/s-0041-1742160
https://doi.org/10.1055/s-0041-1742160
Autor:
Mesut Güngör, Coskun Yarar, Osman Kipoglu, Gulten Ozturk, Cem Paketçi, Kursat Bora Carman, Betül Kılıç, Murat Özkale, Sema Saltik, Hülya Maraş Genç, Erhan Bayram, Pinar Kahraman Koytak, Gunes Sager, Evrim Karadag Saygi, Uluç Yiş, Mehpare Özkan, Bülent Kara, Gazanfer Ekinci, Nihal Olgaç Dündar, Olcay Ünver, Ugur Isik, Dilsad Turkdogan, Serhat Guler, Hatice Gülhan Sözen, Nur Aydınlı, Elif Yüksel Karatoprak, Mine Çalışkan, Ayfer Sakarya Güneş
Publikováno v:
European Journal of Paediatric Neurology. 30:113-120
Aim We aim to describe the demographic characteristics, etiology, neurophysiology, imaging findings, treatment, prognosis, and prognostic factors of acute flaccid myelitis. Methods The clinical data, laboratory test and, magnetic resonance imaging (M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de9976c62c7248003110fb3d24d73423
https://doi.org/10.1016/j.ejpn.2020.10.011
https://doi.org/10.1016/j.ejpn.2020.10.011