Found: 36
Select item for more details and to access through your institution.
Çocuk yoğun bakım ünitesinde izlenen olguların elektroensefalografi sonuçlarının geriye dönük olarak değerlendirilmesi.
- Published in:
- Pamukkale Medical Journal, 2021, v. 14, n. 4, p. 804, doi. 10.31362/patd.822260
- By:
- Publication type:
- Article
Genetic, serological and clinical evaluation of childhood myasthenia syndromes- single center subgroup analysis experience in Turkey.
- Published in:
- Acta Neurologica Belgica, 2023, v. 123, n. 6, p. 2325, doi. 10.1007/s13760-023-02370-3
- By:
- Publication type:
- Article
Evaluation of the Pediatric Neurology Consultations Requested from the Pediatric Emergency Service: A Single-Center Experience.
- Published in:
- Journal of Dr. Behcet Uz Children's Hospital, 2022, v. 12, n. 1, p. 81, doi. 10.4274/buchd.galenos.2021.82713
- By:
- Publication type:
- Article
Evaluation of the Genetically Diagnosed Mitochondrial Disease Cases with Neuromuscular Involvement.
- Published in:
- Journal of Dr. Behcet Uz Children's Hospital, 2022, v. 12, n. 1, p. 27, doi. 10.4274/buchd.galenos.2021.56563
- By:
- Publication type:
- Article
Geç infantil næronal seroid lipofusinoz: Bir olgu sunumu.
- Published in:
- Türk Pediatri Arşivi, 2010, v. 45, n. 2, p. 155, doi. 10.4274/Turk Ped Ars.45.155
- By:
- Publication type:
- Article
Benign paroksismal tortikollis.
- Published in:
- Türk Pediatri Arşivi, 2009, v. 44, n. 1, p. 35
- By:
- Publication type:
- Article
Konjenital musküler distrofili hastalarımızın değerlendirilmesi.
- Published in:
- Türk Pediatri Arşivi, 2009, v. 44, n. 1, p. 23
- By:
- Publication type:
- Article
Evaluation of the Cases with Friedreich Ataxia.
- Published in:
- Gulhane Medical Journal, 2013, v. 55, n. 2, p. 123, doi. 10.5455/gulhane.39786
- By:
- Publication type:
- Article
A novel DOCK7 variant as a rare reason for epileptic encephalopathy, cortical blindness, dysmorphic features: A case report and brief review of the literature.
- Published in:
- Neurology Asia, 2023, v. 28, n. 2, p. 421, doi. 10.54029/2023exu
- By:
- Publication type:
- Article
Red ear syndrome: Three new pediatric cases.
- Published in:
- Neurology Asia, 2022, v. 27, n. 2, p. 521, doi. 10.54029/2022cuw
- By:
- Publication type:
- Article
Evaluation of the body composition with bioelectrical impedence analysia in epileptic patients treated with valproic acid.
- Published in:
- Neurology Asia, 2018, v. 23, n. 2, p. 131
- By:
- Publication type:
- Article
Neuroprotective Effects of Lacosamide and Memantine on Hyperoxic Brain Injury in Rats.
- Published in:
- Neurochemical Research, 2020, v. 45, n. 8, p. 1920, doi. 10.1007/s11064-020-03056-5
- By:
- Publication type:
- Article
Schwartz-Jampel syndrome with gastroduodenal bleeding.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
Optic neuritis in CD59 deficiency: an extremely rare presentation.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
Recurrent painful ophthalmoplegic neuropathy: a report of two new pediatric cases.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
Rotavirus encephalopathy with concomitant acute cerebellitis: report of a case and review of the literature.
- Published in:
- Turkish Journal of Pediatrics, 2020, v. 62, n. 1, p. 119, doi. 10.24953/turkjped.2020.01.017
- By:
- Publication type:
- Article
GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria.
- Published in:
- Turkish Journal of Pediatrics, 2018, v. 60, n. 3, p. 229, doi. 10.24953/turkjped.2018.03.001
- By:
- Publication type:
- Article
Expanding spectrum of SCN1A-related phenotype with novel mutations.
- Published in:
- Turkish Journal of Pediatrics, 2017, v. 59, n. 5, p. 570, doi. 10.24953/turkjped.2017.05.010
- By:
- Publication type:
- Article
Occipital cortex dysgenesis with white matter changes due to mutations in Laminin α2.
- Published in:
- Turkish Journal of Pediatrics, 2017, v. 59, n. 3, p. 338, doi. 10.24953/turkjped.2017.03.018
- By:
- Publication type:
- Article
A case of atypical Miller Fisher syndrome with negative anti-GQ1b immunoglobulin G and importance of H reflex.
- Published in:
- Turkish Journal of Pediatrics, 2013, v. 55, n. 2, p. 235
- By:
- Publication type:
- Article
Pneumatosis intestinalis due to rotavirus infection in a child with Prader-Willi syndrome.
- Published in:
- Turkish Journal of Pediatrics, 2012, v. 54, n. 6, p. 679, doi. 10.24953/turkjped.2012.1711
- By:
- Publication type:
- Article
Evaluation of risk factors for recurrence of cutaneous adverse reactions due to anti-seizure medications in children: A retrospective study.
- Published in:
- Current Journal of Neurology, 2023, v. 22, n. 4, p. 210, doi. 10.18502/cjn.v22i4.14524
- By:
- Publication type:
- Article
Case Report. Importance of acylcarnitine profile analysis for disorders of lipid metabolism in adolescent patients with recurrent rhabdomyolysis: Report of two cases.
- Published in:
- Annals of Indian Academy of Neurology, 2014, v. 17, n. 4, p. 437, doi. 10.4103/0972-2327.144031
- By:
- Publication type:
- Article
Single-center Experience of Therapeutic Plasma Exchange in Children with Neuroimmunological Disorders: Indications, Efficacy, and Safety.
- Published in:
- Anatolian Journal of General Medical Research, 2024, v. 34, n. 1, p. 57, doi. 10.4274/anatoljmed.2023.54521
- By:
- Publication type:
- Article
Characterization and Engineered U1 snRNA Rescue of Splicing Variants in a Turkish Neurodevelopmental Disease Cohort.
- Published in:
- Human Mutation, 2024, v. 2024, p. 1, doi. 10.1155/2024/7760556
- By:
- Publication type:
- Article
Vitamin B12 Deficiency in Pediatric Neurology Practice.
- Published in:
- Haydarpasa Numune Medical Journal, 2023, v. 63, n. 4, p. 377, doi. 10.14744/hnhj.2022.96729
- By:
- Publication type:
- Article
Fibromuscular dysplasia as a cause of stroke in a 9-year-old girl.
- Published in:
- Turkish Journal of Pediatrics, 2011, v. 53, n. 5, p. 567
- By:
- Publication type:
- Article
Anti-GQ1b-negative Miller Fisher syndrome presented with one-sided horizontal gaze palsy.
- Published in:
- Turkish Journal of Pediatrics, 2010, v. 52, n. 3, p. 317
- By:
- Publication type:
- Article
Two cases with megalencephalic leukoencephalopathy with subcortical cysts and MLC1 mutations in the Turkish population.
- Published in:
- 2010
- By:
- Publication type:
- Case Study
Pediatric Pseudotumor Cerebri Syndrome Secondary to Superior Sagittal Sinus Thrombosis Associated with Severe Acute Respiratory Syndrome Coronavirus 2 Infection and Brief Literature Review.
- Published in:
- Journal of Behcet Uz Children's Hospital, 2023, v. 13, n. 3, p. 203, doi. 10.4274/jbuch.galenos.2023.94546
- By:
- Publication type:
- Article
Importance of Skin Changes in the Differential Diagnosis of Congenital Muscular Dystrophies.
- Published in:
- BioMed Research International, 2016, v. 2016, p. 1, doi. 10.1155/2016/3128735
- By:
- Publication type:
- Article
Genetic Landscape of Congenital Myasthenic Syndromes From Turkey: Novel Mutations and Clinical Insights.
- Published in:
- Journal of Child Neurology, 2017, v. 32, n. 8, p. 759, doi. 10.1177/0883073817705252
- By:
- Publication type:
- Article
A Novel Mutation in the Mitochondrial DNA Cytochrome b Gene (MTCYB) in a Patient with Prader Willi Syndrome.
- Published in:
- Journal of Child Neurology, 2015, v. 30, n. 3, p. 378, doi. 10.1177/0883073814530499
- By:
- Publication type:
- Article
Expression Patterns of Micro-RNAs 146a, 181a, and 155 in Subacute Sclerosing Panencephalitis.
- Published in:
- Journal of Child Neurology, 2015, v. 30, n. 1, p. 69, doi. 10.1177/0883073814531329
- By:
- Publication type:
- Article
Importance of Diazepam Administration During Electroencephalography in the Differential Diagnosis of Cortical Visual Loss.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
Temporary Diazepam Responsive Apneic Attacks and Congenital Myasthenic Syndrome.
- Published in:
- Journal of Child Neurology, 2009, v. 24, n. 7, p. 895
- By:
- Publication type:
- Article