Prof. Dr. Nihal Olgaç Dündar

Pediatrik Nöroloji: Algoritmalar ve İlaç Rehberi

Akademisyen Kitabevi eBooks, 2022

DOI 10.37609/akya.2035 Frei zugänglicher VolltextQuelle: OpenAlex

Pediatric Onset Chronic Inflammatory Demyelinating Polyneuropathy: A Multicenter Study from Türkiye

Bursa Uludag University - AVESIS, 2022

Quelle: OpenAlex

Nutritional status and adherence to the mediterranean diet in children with epilepsy

Clinical Nutrition ESPEN, 2022

DOI 10.1016/j.clnesp.2022.02.003 PMID 35331500 7 Zitationen (Europe PMC) Quelle: ORCID

Evaluation of immunization status in patients with cerebral palsy: a multicenter CP-VACC study

European Journal of Pediatrics, 2022

DOI 10.1007/s00431-021-04219-4 PMID 34355277 5 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

A female case of 5,10-methenyltetrahydrofolate synthetase deficiency with novel neuro-imaging abnormalities

Brain and Development, 2022

DOI 10.1016/j.braindev.2022.05.008 PMID 35680490 8 Zitationen (OpenAlex) Quelle: OpenAlex

ITPA Related Developmental Encephalopathy

Annals of Indian Academy of Neurology, 2022

DOI 10.4103/aian.aian_999_21 PMID 35342253 Frei zugänglicher VolltextQuelle: OpenAlex

The impact of Kaizen approach on neurodevelopmental follow-up of high-risk infants

International Journal of Healthcare Management, 2022

DOI 10.1080/20479700.2022.2135068 Quelle: OpenAlex

Editörün Sunuşu

Çocuk ve Medeniyet Dergisi, 2022

Frei zugänglicher VolltextQuelle: OpenAlex

Evaluation of micronutrient levels in children with cerebral palsy

Pediatrics International, 2021

DOI 10.1111/ped.15005 PMID 34585809 9 Zitationen (Europe PMC) Quelle: OpenAlex

SARS-CoV-2 İlişkili Akut Sensorimotor Aksonal Nöropati

Izmir Katip Celebi University Faculty of Medicine, 2021

DOI 10.52818/cjmrtu.2021.5 Frei zugänglicher VolltextQuelle: ORCID

The comparison of regional spinal curvatures and movements in sitting posture in ambulatory children with cerebral palsy having minimal-to-moderate functional limitations

Gait & Posture, 2021

DOI 10.1016/j.gaitpost.2021.09.192 PMID 34571351 Quelle: ORCID

Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia

Brain, 2021

DOI 10.1093/brain/awab041 PMID 33970200 51 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Clinical profile and long-term outcome of the first seizures in children

The Turkish Journal of Pediatrics, 2021

DOI 10.24953/turkjped.2021.04.008 PMID 34449143 10 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

An Unexpected Cause of Ptosis: 22q11.2 Duplication Syndrome

Neurology India, 2021

DOI 10.4103/0028-3886.310061 PMID 33642297 1 Zitation (OpenAlex) Quelle: OpenAlex

Response to "Headache, cataract, and unilateral visual loss: unusual features of DARS2 variants in LBSL" Reply

2021

Quelle: OpenAlex

Effects of epilepsy education on the academic achievement and quality of life of children with epilepsy

British Journal of Neuroscience Nursing, 2021

DOI 10.12968/bjnn.2021.17.6.231 Quelle: OpenAlex

THE EFFECT OF BALANCED DIET AND PHYSICAL ACTIVITY ON THE QUALITY OF LIFE OF UNIVERSITY STUDENTS

Izmir Katip Celebi University Faculty of Medicine, 2021

DOI 10.52818/cjmrtu.2021.19 Frei zugänglicher VolltextQuelle: OpenAlex

THE EFFECT OF SMARTPHONE USE ON SLEEP QUALITY IN IZMIR KÂTIP CELEBI UNIVERSITY STUDENT

Izmir Katip Celebi University Faculty of Medicine, 2021

DOI 10.52818/cjmrtu.2021.10 Frei zugänglicher VolltextQuelle: OpenAlex

Acute flaccid myelitis outbreak through 2016–2018: A multicenter experience from Turkey

European Journal of Paediatric Neurology, 2020

DOI 10.1016/j.ejpn.2020.10.011 PMID 33218883 2 Zitationen (Europe PMC) Quelle: OpenAlex

Investigation of the most common clinical and imaging findings and the role of tubulin genes in the etiology of malformations of cortical development

Turkish Journal of Medical Sciences, 2020

DOI 10.3906/sag-1901-170 PMID 32718119 Frei zugänglicher VolltextQuelle: ORCID

Comparison of the neurocognitive outcomes in term infants treated with levetiracetam and phenobarbital monotherapy for neonatal clinical seizures

Seizure, 2020

DOI 10.1016/j.seizure.2020.06.006 PMID 32540641 15 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

A Neurological Appearance of Celiac Disease

Pediatric Emergency Care, 2020

DOI 10.1097/pec.0000000000001918 PMID 32195978 7 Zitationen (OpenAlex) Quelle: OpenAlex

Variant ataxia-telangiectasia in a child presenting with laryngeal dystonia

The Turkish Journal of Pediatrics, 2020

DOI 10.24953/turkjped.2020.03.019 PMID 32558426 3 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Treatment Outcomes of Pediatric Status Epilepticus in a Tertiary Pediatric Intensive Care Unit

Pediatric Emergency Care, 2020

DOI 10.1097/pec.0000000000001914 PMID 32149989 2 Zitationen (OpenAlex) Quelle: OpenAlex

Topiramate-Responsive Tremor in a Novel Pathogenic Variant of SPG15 Patient

Clinical Neuropharmacology, 2020

DOI 10.1097/wnf.0000000000000392 PMID 32501858 4 Zitationen (OpenAlex) Quelle: OpenAlex

A Case with Neonatal-onset Type 2 Neuronal Ceroid Lipofuscinosis: A Novel Mutation

Journal of College of Physicians And Surgeons Pakistan, 2020

DOI 10.29271/jcpsp.2020.05.543 PMID 32580858 2 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Pediatric case of persistent hiccups associated with hypertrophic olivary degeneration

The Turkish Journal of Pediatrics, 2020

DOI 10.24953/turkjped.2020.02.025 PMID 32419431 1 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Early and Long Term Outcomes of Patients with Diagnosed Acquired Demyelinating Syndromes

The Anatolian Journal of General Medical Research, 2020

DOI 10.5222/terh.2020.48557 Frei zugänglicher VolltextQuelle: OpenAlex

Clinical Outcomes of Apnea in Term Newborns

The Anatolian Journal of General Medical Research, 2020

DOI 10.5222/terh.2020.64326 Frei zugänglicher VolltextQuelle: OpenAlex

Is Exclusive Breastfeeding a Protective Factor Against Idiopathic Epilepsy?

The Anatolian Journal of General Medical Research, 2020

DOI 10.5222/terh.2020.52533 Frei zugänglicher VolltextQuelle: OpenAlex

Auditory event-related potentials demonstrate early cognitive impairment in children with subclinical hypothyroidism

Journal of Pediatric Endocrinology and Metabolism, 2019

DOI 10.1515/jpem-2018-0463 PMID 31194683 5 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

A case of spastic paraplegia-15 with a novel pathogenic variant in ZFYVE26 gene

International Journal of Neuroscience, 2019

DOI 10.1080/00207454.2019.1653293 PMID 31385551 6 Zitationen (Europe PMC) Quelle: ORCID

Impact of next‐generation sequencing panels in the evaluation of limb‐girdle muscular dystrophies

Annals of Human Genetics, 2019

DOI 10.1111/ahg.12319 PMID 31066050 32 Zitationen (OpenAlex) Quelle: OpenAlex

The Clinical and Molecular Characteristics of Molybdenum Cofactor Deficiency Due to MOCS2 Mutations

Pediatric Neurology, 2019

DOI 10.1016/j.pediatrneurol.2019.04.021 PMID 31201073 21 Zitationen (OpenAlex) Quelle: OpenAlex

A new cause of developmental and epileptic encephalopathy with continuous spike-and-wave during sleep: CDKL5 disorder

Neurocase, 2019

DOI 10.1080/13554794.2019.1612923 PMID 31046567 12 Zitationen (OpenAlex) Quelle: OpenAlex

An Option to Consider for Alternating Hemiplegia of Childhood: Aripiprazole

Clinical Neuropharmacology, 2019

DOI 10.1097/wnf.0000000000000339 PMID 30893129 9 Zitationen (OpenAlex) Quelle: OpenAlex

A hypomyelinating leukodystrophy with calcification: oculodentodigital dysplasia

Acta Neurologica Belgica, 2019

DOI 10.1007/s13760-019-01178-4 PMID 31240666 5 Zitationen (OpenAlex) Quelle: OpenAlex

Coincidence of Nemaline Myopathy and Agenesis of Corpus Callosum in a Newborn Infant: Case Report

Journal of Dr Behcet Uz Children s Hospital, 2019

DOI 10.5222/buchd.2019.38801 1 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Amplitüd İntegre Elektroensefalografi ve Klinik Vaka Örnekleri ile Yenidoğanda Amplitüd İntegre Elektroensefalografi Kullanımı

Turkiye Klinikleri Pediatric Sciences - Special Topics, 2019

Quelle: OpenAlex

AMPLITUDE INTEGRATED ELECTROENCEPHALOGRAPHY AND USE OF AMPLITUDE INTEGRATED ELECTROENCEPHALOGRAPHY IN NEWBORN WITH CLINICAL CASE SAMPLES

Turkiye Klinikleri eBooks, 2019

DOI 10.5336/978-605-7650-49-8_p50 Quelle: OpenAlex

A multicenter cross-sectional study to evaluate the clinical characteristics and nutritional status of children with cerebral palsy

Clinical Nutrition Espen, 2018

DOI 10.1016/j.clnesp.2018.05.002 PMID 29908679 26 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

Megalencephalic leukoencephalopathy with subcortical cysts

Neurology, 2018

DOI 10.1212/wnl.0000000000005334 PMID 29661901 73 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Levetiracetam monotherapy for the treatment of infants with epilepsy

Seizure, 2018

DOI 10.1016/j.seizure.2018.02.006 PMID 29453114 20 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Clinical and Genetic Features of Congenital Myasthenic Syndromes due to CHAT Mutations: Case Report and Literature Review

Neuropediatrics, 2018

DOI 10.1055/s-0038-1654706 PMID 29783273 20 Zitationen (OpenAlex) Quelle: OpenAlex

Chromosomal Microarray Analysis in Children with Unexplained Developmental Delay/Intellectual Disability

Journal of Pediatric Genetics, 2018

DOI 10.1055/s-0038-1676583 PMID 30775046 8 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

The first pediatric case of leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL) from Turkey

The Turkish Journal of Pediatrics, 2018

DOI 10.24953/turkjped.2018.02.018 PMID 30325133 6 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

An unusual cause of cavitating leukoencephalopathy: ethylmalonic encephalopathy

Acta Neurologica Belgica, 2018

DOI 10.1007/s13760-018-0902-3 PMID 29464661 4 Zitationen (OpenAlex) Quelle: OpenAlex

Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database

European Journal of Paediatric Neurology, 2017

DOI 10.1016/j.ejpn.2017.06.004 PMID 28694135 23 Zitationen (Europe PMC) Quelle: OpenAlex

Phenotypic profiles in patients with epilepsy-related to SCN1A mutations

European Journal of Paediatric Neurology, 2017

DOI 10.1016/j.ejpn.2017.04.756 Quelle: OpenAlex

Neurological appearance of celiac disease

European Journal of Paediatric Neurology, 2017

DOI 10.1016/j.ejpn.2017.04.1098 Quelle: OpenAlex