Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Şedat IŞIKAY"'
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
Publikováno v:
Arquivos de Gastroenterologia, Vol 52, Iss 4, Pp 272-277 (2015)
Background - Celiac disease is an autoimmune systemic disorder in genetically predisposed individuals precipitated by gluten ingestion. Objective - In this study, we aimed to determine asymptomatic spike-and-wave findings on electroencephalography in
Externí odkaz:
https://doaj.org/article/0541d793ea4b4643abe85b13417be63b
Publikováno v:
Cukurova Medical Journal, Vol 40, Iss 0, Pp 117-121 (2015)
Yenidoğan döneminde bazı metabolik hastalıklar hayatı tehdit eden ensefalopati tablosu olarak ortaya çıkar. Bu durum bazı metabolizma ara ürünlerinin beyinde birikerek toksik etkiler göstermesi ile ilişkilidir. Bebekler doğumda genelde a
Externí odkaz:
https://doaj.org/article/e4958489b9164e2795d8e09e4b3fa4da
Autor:
Sedat IŞIKAY, Halil KOCAMAZ
Publikováno v:
Arquivos de Gastroenterologia, Vol 52, Iss 3, Pp 167-170 (2015)
BackgroundSeveral neurological disorders have also been widely described in celiac disease patients.ObjectiveThe aim of this study was to determine the incidence of accompanying different neurologic manifestations in children with celiac disease at t
Externí odkaz:
https://doaj.org/article/07203814187045bda2cf024b57cc3f03
Publikováno v:
Arquivos de Gastroenterologia, Vol 52, Iss 1, Pp 55-58 (2015)
Background Familial Mediterranean Fever and celiac disease are both related to auto-inflammation and/or auto-immunity and they share some common clinical features such as abdominal pain, diarrhea, bloating and flatulence. Objectives We aimed to deter
Externí odkaz:
https://doaj.org/article/035be56c47dd48d390d1f05b3ab48019
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 40, Iss 1, Pp 117-121 (2015)
On the newborn period some metabolic diseases may cause encephalopathy clinic which can threat the life. This is related with tke accumulation of metabolic intermediates ond the brain and their toxic effects.Babies are usually asymptomatic at birth.
Externí odkaz:
https://doaj.org/article/fd18eccd7d574ccc866c82c2cf07a073
Autor:
Kamil Şahin, Sedat Işıkay
Publikováno v:
Haseki Tıp Bülteni, Vol 54, Iss 1, Pp 44-46 (2016)
Megalencephalic leukoencephalopathy with subcortical cysts, also known as van der Knaap disease, is a rare autosomal recessive disease. The disease develops as a consequence of mutations in the genes MLC1 and MLC2. A three years and nine months ol
Externí odkaz:
https://doaj.org/article/2e45c6e79def4df789c33b44f5066732
Publikováno v:
Arquivos de Gastroenterologia, Vol 52, Iss 2, Pp 134-138 (2015)
Background The involvement of the peripheral nervous system in children with celiac disease is particularly rare. Objective The aim of this study was to assess the need for neurophysiological testing in celiac disease patients without neurological sy
Externí odkaz:
https://doaj.org/article/335d1ac420454528acd0b0455a08535d
Autor:
Ruizhi Duan, Hadia Hijazi, Elif Yilmaz Gulec, Hatice Koçak Eker, Silvia R. Costa, Yavuz Sahin, Zeynep Ocak, Sedat Isikay, Ozge Ozalp, Sevcan Bozdogan, Huseyin Aslan, Nursel Elcioglu, Débora R. Bertola, Alper Gezdirici, Haowei Du, Jawid M. Fatih, Christopher M. Grochowski, Gulsen Akay, Shalini N. Jhangiani, Ender Karaca, Shen Gu, Zeynep Coban-Akdemir, Jennifer E. Posey, Yavuz Bayram, V. Reid Sutton, Claudia M.B. Carvalho, Davut Pehlivan, Richard A. Gibbs, James R. Lupski
Publikováno v:
HGG Advances, Vol 3, Iss 4, Pp 100132- (2022)
Summary: Genetic heterogeneity, reduced penetrance, and variable expressivity, the latter including asymmetric body axis plane presentations, have all been described in families with congenital limb malformations (CLMs). Interfamilial and intrafamili
Externí odkaz:
https://doaj.org/article/335675b4b479443ca3e74cb451032f99
Autor:
Sedat Isikay
Publikováno v:
Annals of Indian Academy of Neurology, Vol 25, Iss 5, Pp 928-930 (2022)
Myokymia is a rare neuromuscular disorder and limb involvement is not common in this disease. To the best of our knowledge, isolated peroneus longus muscle myokymia was not reported before in the literature; and for that reason treatment protocols we
Externí odkaz:
https://doaj.org/article/d2e67b136a91468fa31d96f0899c52d0