Found: 98
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Brain abscess caused by Lactococcus lactis cremoris in a child.
- Published in:
- 2011
- By:
- Publication type:
- journal 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
Nörogörüntülemede Multipl Skleroz İle Karışan Bir Hastalık: Nöro-Behçet.
- Published in:
- Journal of Pediatric Disease / Türkiye Çocuk Hastalıkları Dergisi, 2013, v. 7, p. 47, doi. 10.12956/tjpd.2013.15
- By:
- Publication type:
- Article
Herpes simplex virus-1 as a rare etiology of isolated acute cerebellitis: case report and literature review.
- Published in:
- Journal of NeuroVirology, 2020, v. 26, n. 2, p. 270, doi. 10.1007/s13365-019-00802-6
- By:
- Publication type:
- Article
Mycoplasma pneumoniae: nervous system complications in childhood and review of the literature.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Molecular Diagnosis of Limb-Girdle Muscular Dystrophy Using Next-Generation Sequencing Panels.
- Published in:
- Molecular Syndromology, 2024, v. 15, n. 1, p. 14, doi. 10.1159/000533976
- By:
- Publication type:
- Article
DPAGT1-CDG: Report of Two New Pediatric Patients and Brief Review of the Literature.
- Published in:
- Molecular Syndromology, 2023, v. 14, n. 4, p. 322, doi. 10.1159/000529494
- 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
Sleep Structure in Children With Attention-Deficit/Hyperactivity Disorder.
- Published in:
- Journal of Child Neurology, 2015, v. 30, n. 11, p. 1520, doi. 10.1177/0883073815573318
- 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
Severe Neurologic Involvement of Degos Disease in a Pediatric Patient.
- Published in:
- Journal of Child Neurology, 2014, v. 29, n. 4, p. 550, doi. 10.1177/0883073812474692
- By:
- Publication type:
- Article
Case report of intrafamilial variability in autosomal recessive centronuclear myopathy associated to a novel BIN1 stop mutation.
- Published in:
- Orphanet Journal of Rare Diseases, 2010, v. 5, p. 35, doi. 10.1186/1750-1172-5-35
- By:
- Publication type:
- Article
High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases.
- Published in:
- 2022
- By:
- Publication type:
- journal 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
Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National Study.
- Published in:
- Cerebellum, 2024, v. 23, n. 5, p. 1950, doi. 10.1007/s12311-024-01690-1
- By:
- Publication type:
- Article
Two Young Sisters with Spinocerebellar Ataxia Type 2 Showing Different Clinical Progression of Disease.
- Published in:
- Cerebellum, 2009, v. 8, n. 2, p. 127, doi. 10.1007/s12311-008-0080-6
- 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
The efficacy and safety of levetiracetam in paediatric patients treated with chemotherapeutic agents for haematologic disorders.
- Published in:
- Journal of Paediatrics & Child Health, 2014, v. 50, n. 7, p. 553, doi. 10.1111/jpc.12494
- By:
- Publication type:
- Article
Intravenous levetiracetam for treatment of seizures in term and preterm neonates.
- Published in:
- Journal of Pediatric Neurosciences, 2020, v. 15, n. 1, p. 15, doi. 10.4103/jpn.JPN_66_19
- By:
- Publication type:
- Article
Schwartz-Jampel syndrome with gastroduodenal bleeding.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
Importance of acrocyanosis in delayed walking.
- Published in:
- Journal of Pediatric Neurosciences, 2015, v. 10, n. 1, p. 80, doi. 10.4103/1817-1745.154368
- By:
- Publication type:
- Article
Parieto-occipital encephalomalacia in children; clinical and electrophysiological features of twenty-seven cases.
- Published in:
- Journal of Pediatric Neurosciences, 2015, v. 10, n. 2, p. 103, doi. 10.4103/1817-1745.159187
- By:
- Publication type:
- Article
Kabuki syndrome and perisylvian cortical dysplasia in a Turkish girl.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Coexistence of myositis, transverse myelitis, and Guillain Barré syndrome following Mycoplasma pneumoniae infection in an adolescent.
- Published in:
- 2013
- By:
- Publication type:
- Case Study
Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy and PEHO-like syndrome: Report of two cases.
- Published in:
- 2011
- By:
- Publication type:
- Letter
Multi-cystic white matter enlarged Virchow Robin spaces in a 5-year-old boy.
- Published in:
- 2012
- By:
- Publication type:
- Report
An 11-Year-Old Boy with Headache, Fever, and Neck Pain.
- Published in:
- 2015
- By:
- Publication type:
- journal article
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
VARS1 mutations associated with neurodevelopmental disorder are located on a short amino acid stretch of the anticodon-binding domain.
- Published in:
- Turkish Journal of Biology, 2022, v. 46, n. 6, p. 458, doi. 10.55730/1300-0152.2631
- By:
- Publication type:
- Article
Aicardi syndrome in two Turkish children.
- Published in:
- Annals of Saudi Medicine, 2013, v. 33, n. 1, p. 73, doi. 10.5144/0256-4947.2012.01.7.1545
- By:
- Publication type:
- Article
Cerebellar volume in early-onset schizophrenia and its association with severity of symptoms.
- Published in:
- Journal of International Medical Research, 2019, v. 47, n. 1, p. 411, doi. 10.1177/0300060518803028
- 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
Blood neurofilament light chain and thrombospondin-1 levels of patients with autism spectrum disorder.
- Published in:
- Turkish Journal of Medical Sciences, 2022, v. 52, n. 4, p. 1041, doi. 10.55730/1300-0144.5406
- By:
- Publication type:
- Article
Clinical predictors of drug-resistant epilepsy in children.
- Published in:
- Turkish Journal of Medical Sciences, 2021, v. 51, n. 3, p. 1249, doi. 10.3906/sag-2010-27
- By:
- Publication type:
- Article
Çocukluk Çağı Epilepsisinde Yeni Tanısal Yaklaşımlar: Genetik Alanındaki Gelişmeler Neyi Değiştirdi?
- Published in:
- Turkiye Klinikleri Journal of Pediatrics / Türkiye Klinikleri Pediatri Dergisi, 2016, v. 25, n. 1, p. 34, doi. 10.5336/pediatr.2015-48619
- 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
Electrophysiological Subtypes and Prognostic Factors of Childhood Guillain-Barré Syndrome.
- Published in:
- Archives of Neuropsychiatry / Nöropsikiyatri Arşivi, 2018, v. 55, n. 3, p. 199, doi. 10.5152/npa.2017.16996
- By:
- Publication type:
- Article
Novel insights into PORCN mutations, associated phenotypes and pathophysiological aspects.
- Published in:
- 2022
- By:
- Publication type:
- journal article
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
Rare presentation of levamisole-induced leukoencephalopathy in a pediatric patient: seizure.
- Published in:
- Turkish Journal of Pediatrics, 2021, v. 63, n. 2, p. 319, doi. 10.24953/turkjped.2021.02.017
- By:
- Publication type:
- Article
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
Changes of primary headache related white matter lesions in pediatric patients.
- Published in:
- Turkish Journal of Pediatrics, 2018, v. 60, n. 4, p. 380, doi. 10.24953/turkjped.2018.04.004
- 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
Importance of neurologic and cutaneous signs in the diagnosis of Schimke immuno-osseous dysplasia.
- Published in:
- Turkish Journal of Pediatrics, 2015, v. 57, n. 5, p. 509
- By:
- Publication type:
- Article