Bilimsel çalışmalar

Doç. Dr. Cengiz Havalı

62 yayın. Her yayının yanında bilginin kaynağı yazar.

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  1. Reply to the Letter: "Uncovering the Missing Links: Autoimmunity and Infection in Pediatric Arterial Ischemic Stroke"

    Arquivos de neuro-psiquiatria, 2026

    DOI 10.1055/s-0046-1817047 PMID 41985495 Açık erişimli tam metinKaynak: Europe PMC

  2. Association of Inflammatory and Nutritional Biomarkers in Children with Febrile Seizures: A Case–Control Study of NLR, PNI, and CAR

    Diagnostics, 2026

    DOI 10.3390/diagnostics16162541 PMID 42650945 Açık erişimli tam metinKaynak: ORCID

  3. Psychiatric comorbidity may affect the quality of life in pediatric migraine patients, independently of pain frequency and PedMIDAS score

    Neurology Asia, 2026

    DOI 10.54029/2026xix Açık erişimli tam metinKaynak: ORCID

  4. Circulating Neurogranin and Calmodulin Levels in Children with Epilepsy: A Prospective Case–Control Study

    SSRN Electronic Journal, 2026

    DOI 10.2139/ssrn.7635731 Açık erişimli tam metinKaynak: ORCID

  5. Congenital myasthenic syndromes in Türkiye: genetic and clinical spectrum revisited in a nationwide pediatric cohort

    Neuromuscular Disorders, 2026

    DOI 10.1016/j.nmd.2026.107399 PMID 42727323 1 atıf (OpenAlex) Kaynak: OpenAlex

  6. Acute Disseminated Encephalomyelitis in Children and Adolescents: A Multicenter Retrospective Study of Relapse and Outcome

    Journal of Child Neurology, 2025

    DOI 10.1177/08830738251334219 PMID 40340642 Kaynak: OpenAlex

  7. Central nervous system complications during treatment in childhood acute leukemia

    Acta Neurologica Belgica, 2025

    DOI 10.1007/s13760-024-02602-0 PMID 39192159 1 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  8. Acute arterial ischemic stroke in children: single-center experience

    Arquivos de neuro-psiquiatria, 2025

    DOI 10.1055/s-0045-1809661 PMID 40562371 1 atıf (Europe PMC) Açık erişimli tam metinKaynak: Europe PMC

  9. Psychiatric Comorbidity May Affect the Quality of Life in Pediatric Migraine Patients, Independently of Pain Frequency and Pedmidas Score

    2025

    DOI 10.2139/ssrn.5224649 Kaynak: ORCID

  10. Acute necrotizing encephalopathy associated with RANBP2 mutation: value of MRI findings for diagnosis and intervention

    Acta Neurologica Belgica, 2023

    DOI 10.1007/s13760-022-02166-x PMID 36572756 9 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  11. Acute disseminated encephalomyelitis (ADEM) in children: a multicenter retrospective study

    Kocaeli Üniversitesi - AVESİS, 2022

    Kaynak: OpenAlex

  12. Evaluation of the risk factors for recurrence and the development of epilepsy in patients with febrile seizure

    Arquivos de neuro-psiquiatria, 2022

    DOI 10.1055/s-0042-1755202 PMID 36252585 6 atıf (Europe PMC) Açık erişimli tam metinKaynak: Europe PMC

  13. Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience

    Italian Journal of Pediatrics, 2022

    DOI 10.1186/s13052-022-01349-9 PMID 36076253 15 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  14. Üre döngüsü bozuklukları klinik, laboratuvar ve genetik özellikleri: Tek merkez deneyimi

    Mustafa Kemal Üniversitesi Tıp Dergisi, 2022

    DOI 10.17944/mkutfd.998813 1 atıf (OpenAlex) Açık erişimli tam metinKaynak: ORCID

  15. The management of elevated intracranial pressure and sinus vein thrombosis associated with mastoiditis: the experience of eighteen patients

    Child's Nervous System, 2022

    DOI 10.1007/s00381-021-05402-6 PMID 34713346 5 atıf (Europe PMC) Kaynak: ORCID

  16. Newly defined peroxisomal disease with novel ACBD5 mutation

    Journal of Pediatric Endocrinology and Metabolism, 2022

    DOI 10.1515/jpem-2020-0352 PMID 34668366 10 atıf (Europe PMC) Kaynak: ORCID

  17. Ailelere ve Birinci Basamakta Sağlık Çalışanlarına Yönelik Çocuk Nöroloji

    Akademisyen Kitabevi eBooks, 2022

    DOI 10.37609/akya.1401 Açık erişimli tam metinKaynak: OpenAlex

  18. Outcomes of Inpatient Child Neurology Consultations

    OSMANGAZİ JOURNAL OF MEDICINE, 2021

    DOI 10.20515/otd.1017060 Açık erişimli tam metinKaynak: OpenAlex

  19. Approaches for diagnosis and treatment in neurotransmitter disorders of childhood

    Metabolic Brain Disease, 2021

    DOI 10.1007/s11011-021-00838-w PMID 34550503 2 atıf (Europe PMC) Kaynak: ORCID

  20. Çocuklarda Kortikal Gelişimsel Malformasyonlara Tanısal Yaklaşım: 36 Hastanın Klinik, Görüntüleme ve Laboratuvar Verileri

    Turkish Journal of Pediatric Disease, 2021

    DOI 10.12956/tchd.899026 Açık erişimli tam metinKaynak: ORCID

  21. Recently defined epileptic encephalopathy related to WWOX gene mutation: six patients and new mutations

    Neurological Research, 2021

    DOI 10.1080/01616412.2021.1932173 PMID 34034642 5 atıf (Europe PMC) Kaynak: ORCID

  22. Case series of Arginase 1 deficiency: Expanding the spectrum in hyperargininemia

    Pediatrics International, 2021

    DOI 10.1111/ped.14945 PMID 34343381 2 atıf (Europe PMC) Kaynak: ORCID

  23. The Diagnostic Evaluation of Patients with Hereditary Ataxia in Children: Thirteen Patients and Comprehensive Approach

    Mustafa Kemal Üniversitesi Tıp Dergisi, 2021

    DOI 10.17944/mkutfd.919601 Açık erişimli tam metinKaynak: ORCID

  24. Magnetic resonance imaging patterns of subacute sclerosing panencephalitis may mimic metabolic disorders: clinical, electroencephalographic and imaging features of six cases

    Acta Neurologica Belgica, 2021

    DOI 10.1007/s13760-020-01469-1 PMID 32809122 5 atıf (Europe PMC) Kaynak: ORCID

  25. Rarely Seen Poland–Moebius Syndrome: A Comprehensive View with Perspective of Pediatric Neurology

    Journal of Pediatric Neurology, 2020

    DOI 10.1055/s-0039-1691779 1 atıf (OpenAlex) Kaynak: ORCID

  26. Two different missense mutations of PEX genes in two similar patients with severe Zellweger syndrome: an argument on the genotype-phenotype correlation

    Journal of Pediatric Endocrinology and Metabolism, 2020

    DOI 10.1515/jpem-2019-0194 PMID 32069232 4 atıf (Europe PMC) Kaynak: ORCID

  27. A rare pediatric case of neurobrucellosis with bilateral optic neuritis

    Turkish Journal of Pediatrics, 2020

    DOI 10.24953/turkjped.2020.06.023 PMID 33372450 5 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  28. Cerebral neoplasm in L-2-hydroxyglutaric aciduria: two different presentations

    Child's Nervous System, 2020

    DOI 10.1007/s00381-019-04466-9 PMID 31858216 6 atıf (Europe PMC) Kaynak: ORCID

  29. MRI in CLN2 disease patients: Subtle features that support an early diagnosis

    European Journal of Paediatric Neurology, 2020

    DOI 10.1016/j.ejpn.2020.07.009 PMID 32855042 9 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  30. Two patients with glutaric aciduria type 3: A novel mutation and brain magnetic resonance imaging findings

    Turkish Journal of Pediatrics, 2020

    DOI 10.24953/turkjped.2020.04.017 PMID 32779420 10 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  31. Novel MECR Mutation in Childhood-Onset Dystonia, Optic Atrophy, and Basal Ganglia Signal Abnormalities

    Neuropediatrics, 2019

    DOI 10.1055/s-0039-1688767 PMID 31137067 13 atıf (Europe PMC) Kaynak: ORCID

  32. Temporary seizure in an infant who had been exposed to g-amino butyric acid receptor antagonist thiocolchicoside

    Pediatric Emergency Care, 2019

    DOI 10.1097/pec.0000000000001161 PMID 28486264 2 atıf (Europe PMC) Kaynak: ORCID

  33. A child with atypically subtle clinical presentation of acute arterial ischaemic stroke in the middle cerebral artery

    Interventional Neuroradiology, 2018

    DOI 10.1177/1591019918790241 PMID 30033787 1 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  34. Are diagnostic magnetic resonance patterns life-saving in children with biotin-thiamine-responsive basal ganglia disease?

    European Journal of Paediatric Neurology, 2018

    DOI 10.1016/j.ejpn.2018.06.009 PMID 30054086 6 atıf (Europe PMC) Kaynak: ORCID

  35. Nöronal seroid lipofuksinozis tanılı hastalarda klinik ve genetik özelliklerinin değerlendirilmesi

    Kocaeli Üniversitesi - AVESİS, 2018

    Kaynak: OpenAlex

  36. The efficacy of orbital ultrasonography and magnetic resonance imaging findings with direct measurement of intracranial pressure in distinguishing papilledema from pseudopapilledema

    Child's Nervous System, 2017

    DOI 10.1007/s00381-017-3454-6 PMID 28534259 13 atıf (Europe PMC) Kaynak: ORCID

  37. Two cases of levetiracetam overdose without any serious side effects

    Gazi Medical Journal, 2017

    DOI 10.12996/gmj.2017.39 3 atıf (OpenAlex) Açık erişimli tam metinKaynak: ORCID

  38. Spastic Paraplegia with SPG11 Gene delE39 in a Turkish Patient

    Gazi Medical Journal, 2016

    DOI 10.12996/gmj.2016.64 Açık erişimli tam metinKaynak: ORCID

  39. Ektopik Böbrek ve Dismorfik Bulguları Olan İnfantil Nöroaksonal Distrofi

    Kocaeli Üniversitesi - AVESİS, 2016

    Kaynak: OpenAlex

  40. Does nephrotoxicity exist in pediatric epileptic patients on valproate or carbamazepine therapy?

    Journal of Child Neurology, 2015

    DOI 10.1177/0883073814538505 PMID 24958008 9 atıf (Europe PMC) Kaynak: ORCID

  41. Novel magnetic resonance imaging findings in children with intracranial hypertension

    Pediatric Neurology, 2015

    DOI 10.1016/j.pediatrneurol.2015.03.028 PMID 26101095 26 atıf (Europe PMC) Kaynak: ORCID

  42. Increased Intracranial Hypertension in Children with Novel MRI Findings

    2015

    Kaynak: OpenAlex

  43. İnfeksiyonlar Tetiklenen Tekrarlayan Akut Nekrotizan Ensefalopati: RANBP2 Mutasyonu Saptanan Bir Olgu

    Kocaeli Üniversitesi - AVESİS, 2015

    Kaynak: OpenAlex

  44. Bilateral optik nörit tablosuyla başvuran bir Nörobruselloz vakası

    Kocaeli Üniversitesi - AVESİS, 2015

    Kaynak: OpenAlex

  45. Bir Moebius-Poland Sendromu

    Kocaeli Üniversitesi - AVESİS, 2015

    Kaynak: OpenAlex

  46. İNFEKSİYONLA TETİKLENEN TEKRARLAYAN AKUT NEKROTİZAN ENSEFALOPATİ: RANBP2 MUTASYONU SAPTANAN BİR OLGU

    Kocaeli Üniversitesi - AVESİS, 2015

    Kaynak: OpenAlex

  47. Enfeksiyonla tetiklenen tekrarlayan akut nekrotizan ensefalopati: RANBP2 mutasyonu saptanan bir olgu.

    Kocaeli Üniversitesi - AVESİS, 2015

    Kaynak: OpenAlex

  48. Arterial iskemik inmeli bir çocuk hastada atipik klinik prezentasyon

    Kocaeli Üniversitesi - AVESİS, 2015

    Kaynak: OpenAlex

  49. Herediter spastik paraparezi: SPG11 geninde mutasyon

    Kocaeli Üniversitesi - AVESİS, 2015

    Kaynak: OpenAlex

  50. Nadir görülen bir periodik aparalizi olgusu: Andersen- Tawil Sendromu

    Kocaeli Üniversitesi - AVESİS, 2015

    Kaynak: OpenAlex