Search Results - "Ipek, Rojan"

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  1. 1

    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

    Published in Indian journal of ophthalmology (01-11-2024)
    “…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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    Journal Article
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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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    Journal Article
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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

    Published in Turkish journal of pediatrics (01-07-2021)
    “…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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    Journal Article
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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

    Published in Lokman Hekim Dergisi (28-09-2023)
    “…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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    Journal Article
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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

    Published in Seizure (London, England) (01-08-2022)
    “…Beliefs about health-related problems throughout history are conveyed differently. Unsafe practices based on the superstitious beliefs of patients’ relatives…”
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    Journal Article
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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

    Published in Dicle tıp dergisi (19-09-2024)
    “…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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    Journal Article
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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

    Published in Molecular syndromology (01-04-2023)
    “…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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    Journal Article
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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

    Published in Metabolic brain disease (01-12-2022)
    “…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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    Journal Article
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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

    Published in Acta neurologica Belgica (01-08-2024)
    “…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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    Journal Article
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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

    Published in Dicle tıp dergisi (13-06-2022)
    “…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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    Journal Article
  13. 13

    Evaluation of developmental profiles of children with hydrocephalus by Gönüllü Polat, Burçin, Makharoblidze, Khatuna, İpek, Rojan, Çobanoğullari Direk, Meltem, Derici Yıldırım, Didem, Okuyaz, Çetin

    Published in Neurocirugía (Asturias, Spain) (01-11-2022)
    “…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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    Journal Article
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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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    Journal Article
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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

    Published in Molecular syndromology (01-04-2023)
    “…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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