Search Results - "Ozturk, Selcan"

Evaluation of immunization status in patients with cerebral palsy: a multicenter CP-VACC study by Bozkaya-Yilmaz, Sema, Karadag-Oncel, Eda, Olgac-Dundar, Nihal, Gencpinar, Pinar, Sarioglu, Berrak, Arican, Pinar, Ersen, Atilla, Yilmaz-Ciftdoğan, Dilek, Yuksel, Merve Feyza, Bektas, Omer, Teber, Serap, Kilic, Betul, Calik, Mustafa, Karaca, Meryem, Canpolat, Mehmet, Kumandas, Sefer, Per, Huseyin, Gumus, Hakan, Ozturk, Selcan, Okuyaz, Cetin, Komur, Mustafa, Ipek, Rojan, Ozbudak, Pınar, Arhan, Ebru, Ince, Hulya, Gurbuz, Gurkan, Mert, Gulen Gul, Ozcan, Neslihan, Turker, Akgun Olmez, Gazeteci-Tekin, Hande, Kırık, Serkan, Günbey, Ceren, Çarman, Kürşat Bora, Yarar, Coşkun, Çavuşoğlu, Dilek

“…Children with chronic neurological diseases, including cerebral palsy (CP), are especially susceptible to vaccine-preventable infections and face an increased…”
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Tracheobronchial Foreign Body Aspiration in Childhood by Doğan, Murat, Esen, Feyza, Doğan, Yasemin, Öztürk, Selcan, Demir, Ömer Faruk, Öztürk, Mehmet Adnan

“…Objective: The aim of this study was to determine the patients who were followed up and treated in pediatric emergency service due to foreign body aspiration…”
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An Evaluation of Previously Undiagnosed Childhood Primary Headache Cases Through Their EEG and MR Findings by Ozturk, Selcan, Komut, Erdal

“…Aim: Headaches are a major cause of presentations to pediatric neurology clinics, the majority being primary. Although diagnosis is mostly based on medical…”
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Congenital Myasthenic Syndromes in Turkey: Clinical and Molecular Characterization of 16 Cases With Three Novel Mutations by Öztürk, Selcan, Güleç, Ayten, Erdoğan, Murat, Demir, Mikail, Canpolat, Mehmet, Gümüş, Hakan, Çağlayan, Ahmet Okay, Dündar, Munis, Per, Hüseyin

“…Congenital myasthenic syndromes (CMS) are composed of numerous hereditary disorders involving genetic mutations in proteins essential to the integrity of…”
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A Rare Cause of Hypotonia: 49,XXXXX (Pentasomy X): A Rare Cause of Hypotonia: 49,XXXXX (Pentasomy X) by Aydoğan, Kübra, Öztürk, Selcan, Dündar, Munis, Gümüş, Hakan, Saatçi, Çetin, Per, Hüseyin

“…Pentasomy X syndrome is a very rare sex chromosome numerical anomaly of unknown frequency. The karyotype consists of 49,XXXXX. Musculoskeletal, craniofacial,…”
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Anxiety and healthcare satisfaction of mothers with children hospitalized in the pediatric emergency service by Efe, Yağmur Sezer, Erdem, Emine, Doğan, Murat, Bağcı, Kazım, Öztürk, Selcan, Öztürk, M Adnan

“…This cross-sectional study was conducted to determine the anxiety and healthcare satisfaction levels of mothers with children hospitalized in the pediatric…”
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Pediatric-Onset Chronic Inflammatory Demyelinating Polyneuropathy: A Multicenter Study by Sarıkaya Uzan, Gamze, Vural, Atay, Yüksel, Deniz, Aksoy, Erhan, Öztoprak, Ülkühan, Canpolat, Mehmet, Öztürk, Selcan, Yıldırım, Çelebi, Güleç, Ayten, Per, Hüseyin, Gümüş, Hakan, Okuyaz, Çetin, Çobanoğulları Direk, Meltem, Kömür, Mustafa, Ünalp, Aycan, Yılmaz, Ünsal, Bektaş, Ömer, Teber, Serap, Aliyeva, Nargiz, Olgaç Dündar, Nihal, Gençpınar, Pınar, Gürkaş, Esra, Keskin Yılmaz, Sanem, Kanmaz, Seda, Tekgül, Hasan, Aksoy, Ayşe, Öz Tuncer, Gökçen, Acar Arslan, Elif, Tosun, Ayşe, Ayanoğlu, Müge, Kızılırmak, Ali Burak, Yousefi, Mohammadreza, Bodur, Muhittin, Ünay, Bülent, Hız Kurul, Semra, Yiş, Uluç

“…To evaluate the clinical features, demographic features, and treatment modalities of pediatric-onset chronic inflammatory demyelinating polyneuropathy (CIDP)…”
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Shuddering attacks in children: A retrospective analysis of 19 cases from a single-center in Turkey by Ozturk, Selcan, Peduk, Yakup, Gumus, Hakan, Per, Huseyin

“…•Shuddering attacks (SA) are nonepileptic, paroxysmal, fast, and short motor events.•Shuddering attacks usually start during the 4th–6th months of life.•Mostly…”
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Therapeutic implications of etiology-specific diagnosis of early-onset developmental and epileptic encephalopathies (EO-DEEs): A nationwide Turkish cohort study by Kanmaz, Seda, Tekgul, Hasan, Kayilioglu, Hulya, Atas, Yavuz, Kart, Pinar Ozkan, Yildiz, Nihal, Gumus, Hakan, Aydin, Kursad, Kanmaz, Seda, Olculu, Cemile Busra, Dogan, Dilara Ece Toprak, Per, Huseyin, Canpolat, Mehmet, Gulec, Ayten, Yildirim, Nalan, Turk, Emre, Celik, Neslihan, Ozturk, Selcan, Kumandas, Sefer, Kilic, Betul, Topcu, Yasemin, Ozpinar, Esra, Coskun, Aysenur, Arslan, Mutluay, Akkoyunlu, Deniz Sunnetci, Cine, Naci, Uzan, Gamze Sarikaya, Gunay, Cagatay, Akyol, Duygu, Ersoy, Ozlem, Direk, Meltem Cobanogullari, Komur, Mustafa, Kirkgoz, Hilal, Karaoğlu, Pakize, Ibis, Ipek Burcu Parlak, Cerci, Cisil, Orak, Ali, Oktay, Secil, Ayanoglu, Muge, Yildirim, Mirac, Bektas, Omer, Serdaroglu, Esra, Yilmaz, Sema Bozkaya, Cankurt, Ilknur, Hirfanoglu, Tugba, Arhan, Ebru, Gencpinar, Pinar, Dundar, Nihal Olgac, Teber, Serap, Serin, Hepsen Mine, Yilmaz, Sanem, Tosun, Ayse, Polat, Muzaffer, Yilmaz, Unsal, Unalp, Aycan, Kara, Bulent, Okuyaz, Cetin, Yis, Uluc, Hiz, Semra, Aktan, Gul, Gokben, Sarenur, Unay, Bulent, Serdaroglu, Ayse, Cansu, Ali

“…•Gene-related EO-DEEs are 48.3 % in the nationwide-Turkish cohort.•Common non-structural genetic variants are SCN1A, CDKL5, STXBP, KCNQ2, and…”
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Çocukluk çağındaki trakeobronşiyal yabancı cisim aspirasyonları by Doğan,Murat, Esen,Feyza, Doğan,Yasemin, Öztürk,Selcan, Demir,Ömer Faruk, Öztürk,Mehmet Adnan

“…Amaç: Yabancı cisim aspirasyonu (YCA) nedeniyle çocuk acil servisinde takip ve tedavi edilen hastaların değerlendirmesi amaçlanmıştır. Yöntemler: 2017 yılı…”
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