Zobrazeno 1 - 10
of 88
pro vyhledávání: '"Coskun Yarar"'
Autor:
Kursat Bora Carman, Mustafa Calik, Yasemin Karal, Sedat Isikay, Ozan Kocak, Aysima Ozcelik, Ahmet Sami Yazar, Cagatay Nuhoglu, Cigdem Sag, Omer Kilic, Meltem Dinleyici, Sibel Lacinel Gurlevik, Sevgi Yimenicioglu, Arzu Ekici, Peren Perk, Ayse Tosun, Ilhan Isik, Coskun Yarar, Didem Arslantas, Ener Cagri Dinleyici
Publikováno v:
Human Vaccines & Immunotherapeutics, Vol 15, Iss 2, Pp 496-502 (2019)
Background: Febrile seizure is the most common childhood neurological disorder, is an important health problem with potential short- and long-term complications, also leading to economic burden and increased parental anxiety about fevers and seizures
Externí odkaz:
https://doaj.org/article/4d4b6bfa11c349df8e837a9ede679949
Autor:
Ebru Kacmaz, Gurkan Bozan, Kursat Bora Carman, Omer Kilic, Mehmet Ozgur Arslanoglu, Ugur Toprak, Aslı Kavaz Tufan, Coskun Yarar, Ener Cagri Dinleyici
Publikováno v:
Case Reports in Pediatrics, Vol 2021 (2021)
Acute disseminated encephalomyelitis (ADEM) is an inflammatory, demyelinating, and rapidly progressive disorder of the central nervous system. This condition is also known as postinfectious encephalomyelitis, and it is characterized by multifocal les
Externí odkaz:
https://doaj.org/article/b2eead33f5e84a21a904bce996ae52f6
Autor:
Meltem Dinleyici, Kursat Bora Carman, Omer Kilic, Sibel Laciner Gurlevik, Coskun Yarar, Ener Cagri Dinleyici
Publikováno v:
Human Vaccines & Immunotherapeutics, Vol 14, Iss 8, Pp 1970-1976 (2018)
The aim of this study was to evaluate the age-appropriate immunization coverage in 366 children with chronic neurological disease (CND), to evaluate the use of vaccines not included in routine program, to evaluate serological tests for vaccine-preven
Externí odkaz:
https://doaj.org/article/237e732d38394cebbd377c580d1560dd
Publikováno v:
Annals of Indian Academy of Neurology, Vol 19, Iss 3, Pp 388-391 (2016)
Hemophagocytic lymphohistiocytosis (HLH) is a rare lymphoproliferative disorder. HLH may occur as a complication of Epstein-Barr virus (EBV), particularly in patients with immunodeficiencies. Herein, we describe a 16-year-old girl with neurological c
Externí odkaz:
https://doaj.org/article/9d3f9b6a77fc46d49051f307a84e7347
Autor:
Kursat Bora Carman, Coskun Yarar, Ener Cagri Dinleyici, Gürkan Bozan, Suzan Saylisoy, Eylem Kiral, Omer Kilic, Merve Işeri Nepesov
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
JCRPE, Vol 13, Iss 3, Pp 358-361 (2021)
JCRPE, Vol 13, Iss 3, Pp 358-361 (2021)
Brain abscess formation is extremely rare in patients with osteopetrosis. Herein, we report a case of viridans streptococci brain abscess in an immunocompromised child diagnosed with osteopetrosis. The patient presented with a sudden change in mental
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
Publikováno v:
Journal of Pediatric Neurology. 20:224-226
Charcot-Marie-Tooth (CMT) disease is a group of clinically and genetically heterogeneous peripheral neuropathies by causing distal muscle weakness, sensory impairment, hyporeflexia, and skeletal deformities. Both of sequence and copy number variation
Autor:
Kursat Bora Carman, Hirotomo Saitsu, Naomichi Matsumoto, Ozan Kocak, Coskun Yarar, Hirofumi Kodera
Publikováno v:
Tropical Health and Medical Research. 2:18-25
Perinatal arterial ischemic stroke (PAIS) is one of the frequent causes of mortality and morbidity, but its etiology remains unclear. COL4A1 and COL4A2 mutations are monogenetic causes of weakness of the basement vascular membranes resulting in cereb
Autor:
Koray Harmanci, Meltem Dinleyici, Makbule Eren, Birgül Kirel, Coskun Yarar, Enver Simsek, Figen Şahin Dağlı, Kursat Bora Carman, Aysu Duyan Çamurdan, Canan Özdemir
Publikováno v:
Balkan Medical Journal, Vol 37, Iss 1, Pp 34-42 (2020)
Balkan Medical Journal
Balkan Medical Journal
Background: Chronic disease of children can cause changes in the health-related quality of life (HrQoL) of the family members. Aims: To evaluate the HrQoL of healthy siblings of children with chronic disease. Study Design: Cross-sectional study. Meth
Autor:
Bülent Ünay, Esra Gürkaş, Meral Karadag, Ozgen Hur, Cefa Nil Karademir, Nihal Olgaç Dündar, Yakup Peduk, Mine Serin, Ali Cansu, Gonca Kılıç Yıldırım, Çetin Okuyaz, Coskun Yarar, Hasan Tekgul, Kürşad Aydın, Kursat Bora Carman, Betul Kilic Aydin, Pınar Özkan Kart, Serdal Güngör, Pinar Gencpinar, Selver Durmus, Nefise Arıbas Oz, Hüseyin Per, Meltem Çobanoğulları Direk
Background Many studies evaluating the nutritional status of children with cerebral palsy (CP) have focused on energy requirements and protein intake. The present work aimed to assess nutritional status and micronutrient levels of children with (CP).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::309cc4bbeb2da9058ebfaaf1ef2075f8
https://hdl.handle.net/11454/77591
https://hdl.handle.net/11454/77591