Akademisyen

CENGİZ DİLBER

PROFESÖR

KAHRAMANMARAŞ SÜTÇÜ İMAM ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ

Ana Dal Sağlık Bilimleri Temel Alanı
Yan Dal Çocuk Nörolojisi (Çocuk Sağlığı ve Hastalıkları)

Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.

Makale 66
Proje 0
Kitap 0
Bildiri 0
Patent 0
Sanatsal 0

Scopus (SJR) Q1 20 Q2 14 Q3 10 Q4 5

WoS (JCR) Q1 9 Q2 11 Q3 15 Q4 11

TR Index 4 makale

Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.

Üst %1 makale 0

Üst %10 makale 0

Ort. yüzdelik 43.0%

Üst %1 payı 0.0%

Üst %10 payı 0.0%

Makaleler

YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.

Makale listesi

2025 Corrigendum to "Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes" Europ. J. Paediatr. Neurol DOI 10.1016/j.ejpn.2022.08.006 YÖKSİS SJR Q1 JCR Q1
2024 The effect of proprioceptive neuromuscular facilitation on functional skills, muscle strength, and trunk control in children with cerebral palsy: A randomized controlled trial Early Human Development DOI 10.1016/j.earlhumdev.2024.106010 YÖKSİS SJR Q1 JCR Q2
2024 Distinctive sleep complaints and polysomnographic findings in antibody subgroups of autoimmune limbic encephalitis Neurological Sciences DOI 10.1007/s10072-024-07652-z YÖKSİS SJR Q1 JCR Q3 OpenAlex 71.9%
2024 Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National Study The Cerebellum DOI 10.1007/s12311-024-01690-1 YÖKSİS SJR Q1 JCR Q3
2024 Corrigendum to "Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes" EUROPEAN JOURNAL OF PEDİATRİC NEUROLOGY DOI 10.1016/j.ejpn.2024.11.006 YÖKSİS SJR Q1 JCR Q2
2023 Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study Neuropediatrics DOI 10.1055/a-2034-8528 YÖKSİS SJR Q2 JCR Q3
2022 Novel homozygous AP3B2 mutations in four individuals with developmental and epileptic encephalopathy: A rare clinical entity Clinical Neurology and Neurosurgery DOI 10.1016/j.clineuro.2022.107509 YÖKSİS SJR Q2 JCR Q3
2022 Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes Eur J Paediatr Neurol DOI 10.1016/j.ejpn.2022.08.006 YÖKSİS SJR Q1 JCR Q2
2022 Therapeutic Plasma Exchange in Pediatric Patients: Results from a Single Center Journal of Pediatric Intensive Care DOI 10.1055/s-0041-1742252 YÖKSİS SJR Q4 JCR Q4
2021 Predictive value of cardiac markers in the prognosis of COVID-19 in children The American Journal of Emergency Medicine DOI 10.1016/j.ajem.2021.06.075 YÖKSİS SJR Q1 JCR Q1
2021 Predictive value of cardiac markers in the prognosis of COVID-19 in children Am J Emerg Med DOI 10.1016/j.ajem.2021.06.075 YÖKSİS SJR Q1 JCR Q1
2021 Evaluation of oxidative stress biomarkers in acute mercury intoxication Folia Medica DOI 10.3897/folmed.63.e56110 YÖKSİS SJR Q4
2021 Evaluation of oxidative stress biomarkers in acute mercury intoxication Folia Medica DOI 10.3897/folmed.63.e56110 YÖKSİS SJR Q4 OpenAlex 14.0%
2020 Vanishing white matter disease with different faces Child's Nervous System DOI 10.1007/s00381-019-04334-6 YÖKSİS SJR Q2 JCR Q4
2018 A multicenter cross-sectional study to evaluate the clinical characteristics and nutritional status of children with cerebral palsy clinical nutrition DOI 10.1016/clnesp.2018.05.002 YÖKSİS SJR Q3 JCR Q3
2017 Exome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsy Acta Neurologica Belgica DOI 10.1007/s13760-016-0721-3 YÖKSİS SJR Q3 JCR Q3
2017 A new mutation in an infant with Krabbe disease accompanied by enlargement of the optic nerves Acta Neurologica Belgica DOI 10.1007/s13760-016-0637-y YÖKSİS SJR Q3 JCR Q3
2016 Acute Mercury Poisoning in a Group of School Children Pediatric Emergency Care DOI 10.1097/PEC.0000000000001011 YÖKSİS SJR Q2 JCR Q3
2016 Thalamic T2 hypointensity: a diagnostic clue for Tay–Sachs disease Acta Neurologica Belgica DOI 10.1007/s13760-015-0538-5 YÖKSİS SJR Q3 JCR Q3
2016 A compound heterozygous EARS2 mutation associated with mild leukoencephalopathy with thalamus and brainstem involvement and high lactate (LTBL) Brain and Development DOI 10.1016/j.braindev.2016.04.002 YÖKSİS SJR Q2 JCR Q4

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