Academician profile · PROFESÖR
BÜLENT KARA
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Çocuk Nörolojisi (Çocuk Sağlığı ve Hastalıkları)
- TIP FAKÜLTESİ
- DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
Scopus (SJR)
Q1
43
Q2
23
Q3
14
Q4
9
WoS (JCR)
Q1
21
Q2
27
Q3
19
Q4
21
TR Index
10
articles
Articles
- 2022 Reversible Splenial Lesion Syndrome and Multisystem Inflammatory Syndrome Findings in a Child with SARS-COV-2 Infection
- 2022 Clinical and Electrophysiological Characteristics of Patients with Juvenile Absence Epiplepsy in a Turkish Cohort
- 2022 West Sendromlu Olgularda Acth Tedavisinin Etkinliği ve Kemik Mineral Metabolizması ve Adrenal Yolak Üzerine Uzun Dönem Etkileri
- 2021 Acute flaccid myelitis outbreak through 2016–2018: A multicenter experience from Turkey
- 2021 Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals
- 2021 Distinct gene-set burden patterns underlie common generalized and focal epilepsies
- 2021 Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations
- 2021 Clinical and electrophysiological predictors of behavioral disorders in patients with benign childhood epilepsy with centrotemporal spikes
- 2021 Cytotoxic lesions of the corpus callosum in children: Etiology, clinical and radiological features, and prognosis
- 2021 Compound Heterozygous ROBO3 Mutation in Two Siblings Presenting with Horizontal Gaze Palsy without Scoliosis: Case-Based Review
- 2021 Could Maternal COVID-19 Disease be a Risk Factor for Neurodevelopmental Disorders in the Child?
- 2021 Autoimmune Hemolytic Anemia Due to Spondyloenchondrodysplasia with Spastic Paraparesis and Intracranial Calcification due to Mutation in ACP5
- 2020 Early-onset rapidly progressive myoclonic epilepsy associated with G392R likely pathogenic variant in SERPINI1
- 2020 Monogenic lupus due to spondyloenchondrodysplasia with spastic paraparesis and intracranial calcification: case-based review
- 2020 A Novel Mutation of HINT1 Gene in an Adolescent Female with Axonal Neuropathy and Neuromyotonia
- 2020 Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects
- 2020 SCREENING SLC2A1 GENE FOR SEQUENCE AND COPY NUMBER VARIATIONS ASSOCIATED WITH GLUT-1 DEFICIENCY SYNDROME
- 2019 FAM160B1 deficit associated with microcephaly, severe intellectual disability, ataxia, behavioral abnormalities and speech problems
- 2019 Polygenic burden in focal and generalized epilepsies
- 2019 Gıda Katkılarının Çocuk Sağlkığı Üzerine Etkileri