Search Results - "Ipek, Rojan"
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Alterations in the tear film and ocular surface in pediatric migraine patients
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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Evaluation of immunization status in patients with cerebral palsy: a multicenter CP-VACC study
Published in European journal of pediatrics (2022)“…Children with chronic neurological diseases, including cerebral palsy (CP), are especially susceptible to vaccine-preventable infections and face an increased…”
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A Case Report of a New Variant Associated with Vici Syndrome in a Turkish Infant; EPG5 Frameshift Variant
Published in Majallah-ʼi bīmārīhā-yi kūdakān-i Īrān = Iranian journal of pediatrics (09-11-2024)“…Introduction: Vici syndrome is a congenital multisystem disorder characterized primarily by callosal agenesis, cataracts, cardiomyopathy, combined…”
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Developmental evaluation in children experiencing febrile convulsions
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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Vitamin D Levels in Children Presenting with Breath-Holding Spells: An Example of A University Hospital
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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A Rare Case of Rotavirus-related Acute Benign Myositis
Published in The Pediatric infectious disease journal (01-10-2023)Get full text
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7
Beliefs and behaviors of patients' relatives towards childhood epilepsy in Turkey
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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Evaluation of Etiological Causes and Demographic Characteristics of Neonatal Seizure in Adiyaman University Training And Research Hospital, Türkiye: A Retrospective Study
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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Case Report of Two Siblings Diagnosed with Osteogenesis Imperfecta Type XV with a New Mutation in the WNT1 Gene and Review of the Literature
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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10
Pyridoxine-dependent Epilepsy caused by a Novel homozygous mutation in PLPBP Gene
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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11
Could headache in children be a biomarker for dyslipidemia?
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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12
Isolated neuro-Behçet’s disease in a child, from headache to diagnosis: A case report
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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13
Evaluation of developmental profiles of children with hydrocephalus
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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14
Biallelic NAA60 variants with impaired N-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications
Published in Nature communications (13-03-2024)“…Primary familial brain calcification (PFBC) is characterized by calcium deposition in the brain, causing progressive movement disorders, psychiatric symptoms,…”
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15
A Multicenter Study of Self-Limited Epilepsy With Centrotemporal Spikes: Effectiveness of Antiseizure Medication With Respect to Spike-Wave Index
Published in Pediatric neurology (01-03-2024)“…There is no certain validated electroencephalographic (EEG) parameters for outcome prediction in children with self-limited epilepsy with centrotemporal…”
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16
Evaluation of developmental profiles of children with hydrocephalus
Published in Neurocirugía (Barcelona. Internet. English ed.) (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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17
Case Report of Two Siblings Diagnosed with Osteogenesis Imperfecta Type XV with a New Mutation in the WNT1 Gene and Review of the Literature
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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A Rare Case of Rotavirus-related Acute Benign Myositis
Published in The Pediatric infectious disease journal (01-10-2023)Get full text
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