Search Results - "İPEK, Rojan"

Alterations in the tear film and ocular surface in pediatric migraine patients by Asik, Abdulvahit, Aksoy Aydemir, Gözde, Aydemir, Emre, Bilen, Abdurrahman, Ipek, Rojan, Ballı, Hacı, Bayat, Alper Halil, Türk, Bilge Aydın

“…To evaluate the ocular surface (OS) parameters in the pediatric migraine patients (PMPs). This prospective case-control study consisted of 51 PMPs (PMP group)…”
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Vitamin D Levels in Children Presenting with Breath-Holding Spells: An Example of A University Hospital by İPEK, Rojan, VARAN, Celal

“…Aim: This study aimed to examine the vitamin D levels in children who experience breath-holding spells (BHS) and to compare these levels with those of a…”
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A Rare Case of Rotavirus-related Acute Benign Myositis by Kilic, Fedli Emre, İpek, Rojan, Almiş, Habip

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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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Beliefs and behaviors of patients' relatives towards childhood epilepsy in Turkey by Okuyaz, Selda, İpek, Rojan, Ögenler, Oya, Yıldırım, Didem Derici, Okuyaz, Çetin

“…Beliefs about health-related problems throughout history are conveyed differently. Unsafe practices based on the superstitious beliefs of patients’ relatives…”
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Evaluation of Etiological Causes and Demographic Characteristics of Neonatal Seizure in Adiyaman University Training And Research Hospital, Türkiye: A Retrospective Study by İpek, Rojan, Akar, Selahattin, Aşık, Abdulvahit, Ballı, Haci

“…Aim: Neonatal seizures are different from seizures seen at other ages in terms of etiology, clinical follow-up, treatment and prognosis. The purpose of this…”
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Case Report of Two Siblings Diagnosed with Osteogenesis Imperfecta Type XV with a New Mutation in the WNT1 Gene and Review of the Literature by Çavdartepe, Büşra Eser, İpek, Rojan

“…Introduction: Osteogenesis imperfecta (OI) is a heritable disorder characterized by bone fractures and low bone mass. Recently, mutations of the WNT1 gene have…”
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Pyridoxine-dependent Epilepsy caused by a Novel homozygous mutation in PLPBP Gene by İpek, Rojan, Çavdartepe, Büşra Eser, Kor, Deniz, Okuyaz, Çetin

“…Seizures in newborn infants may be the first finding of hereditary metabolic diseases. Pyridoxine-dependent epilepsy (PDE) is a treatable disorder associated…”
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Could headache in children be a biomarker for dyslipidemia? by İpek, Rojan, Varan, Celal, Kılıç, Fedli Emre, Alagöz Karabel, Müsemma, Almiş, Habip

“…Aim Here we present the patients whose body mass index is in the normal range and who visited with the complaint of headache. The differences in lipid profile…”
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Isolated neuro-Behçet’s disease in a child, from headache to diagnosis: A case report by İPEK, Rojan, TEN, Barıs, KÖMÜR, Mustafa, OKUYAZ, Cetin

“…Behçet's disease (BD) is an immuno-inflammatory multi-systemic disease characterized by ophthalmological and skin involvement, also oral and genital ulcers…”
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Evaluation of developmental profiles of children with hydrocephalus by Gönüllü Polat, Burçin, Makharoblidze, Khatuna, İpek, Rojan, Çobanoğullari Direk, Meltem, Derici Yıldırım, Didem, Okuyaz, Çetin

“…The objective of this study was to compare the developmental characteristics of children with hydrocephalus with those of healthy children. A total of 109…”
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Biallelic NAA60 variants with impaired N-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications by Chelban, Viorica, Aksnes, Henriette, Maroofian, Reza, LaMonica, Lauren C., Seabra, Luis, Siggervåg, Anette, Devic, Perrine, Shamseldin, Hanan E., Vandrovcova, Jana, Murphy, David, Richard, Anne-Claire, Quenez, Olivier, Bonnevalle, Antoine, Zanetti, M. Natalia, Kaiyrzhanov, Rauan, Salpietro, Vincenzo, Efthymiou, Stephanie, Schottlaender, Lucia V., Morsy, Heba, Scardamaglia, Annarita, Tariq, Ambreen, Pagnamenta, Alistair T., Pennavaria, Ajia, Krogstad, Liv S., Bekkelund, Åse K., Caiella, Alessia, Glomnes, Nina, Brønstad, Kirsten M., Tury, Sandrine, Moreno De Luca, Andrés, Boland-Auge, Anne, Olaso, Robert, Deleuze, Jean-François, Anheim, Mathieu, Cretin, Benjamin, Vona, Barbara, Alajlan, Fahad, Abdulwahab, Firdous, Battini, Jean-Luc, İpek, Rojan, Bauer, Peter, Zifarelli, Giovanni, Gungor, Serdal, Kurul, Semra Hiz, Lochmuller, Hanns, Da’as, Sahar I., Fakhro, Khalid A., Gómez-Pascual, Alicia, Botía, Juan A., Wood, Nicholas W., Horvath, Rita, Ernst, Andreas M., Rothman, James E., McEntagart, Meriel, Crow, Yanick J., Alkuraya, Fowzan S., Nicolas, Gaël, Arnesen, Thomas, Houlden, Henry

“…Primary familial brain calcification (PFBC) is characterized by calcium deposition in the brain, causing progressive movement disorders, psychiatric symptoms,…”
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A Multicenter Study of Self-Limited Epilepsy With Centrotemporal Spikes: Effectiveness of Antiseizure Medication With Respect to Spike-Wave Index by Dilber, Beril, Serdaroğlu, Esra, Kanmaz, Seda, Kılıç, Betül, İpek, Rojan, Menderes, Deniz Kargın, Yıldız, Nihal, Topçu, Yasemin, Arhan, Ebru Petek, Serdaroğlu, Ayşe, Okuyaz, Çetin, Aydın, Kürşad, Tekgül, Hasan, Cansu, Ali

“…There is no certain validated electroencephalographic (EEG) parameters for outcome prediction in children with self-limited epilepsy with centrotemporal…”
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Evaluation of developmental profiles of children with hydrocephalus by Gönüllü Polat, Burçin, Makharoblidze, Khatuna, İpek, Rojan, Çobanoğullari Direk, Meltem, Derici Yıldırım, Didem, Okuyaz, Çetin

“…The objective of this study was to compare the developmental characteristics of children with hydrocephalus with those of healthy children. A total of 109…”
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A Case Report of a New Variant Associated with Vici Syndrome in a Turkish Infant; EPG5 Frameshift Variant by Ipek, Rojan, Eser Çavdartepe, Büşra, Hazar, Leyla

“…Introduction: Vici syndrome is a congenital multisystem disorder characterized primarily by callosal agenesis, cataracts, cardiomyopathy, combined…”
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Case Report of Two Siblings Diagnosed with Osteogenesis Imperfecta Type XV with a New Mutation in the WNT1 Gene and Review of the Literature by Çavdartepe, Büşra Eser, İpek, Rojan

“…IntroductionOsteogenesis imperfecta (OI) is a heritable disorder characterized by bone fractures and low bone mass. Recently, mutations of the WNT1 gene have…”
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A Rare Case of Rotavirus-related Acute Benign Myositis by Kilic, Fedli Emre, İpek, Rojan, Almiş, Habip

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Developmental evaluation in children experiencing febrile convulsions by İpek, Rojan, Makharoblidze, Khatuna, Polat, Burçin Gönüllü, Direk, Meltem Çobanoğulları, Yıldırım, Didem Derici, Kömür, Mustafa, Okuyaz, Çetin

“…Background. The objective of this study was to determine the effect of febrile convulsion (FC) on neuromotor development. Methods. Data of 325 patients, who…”
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