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Adamantios Katerelos

Observed names: Katerelos Adamantios, Αδαμάντιος Κατερέλος
ORCID: 0000-0002-7032-9907
Observed ORCID: 0000-0002-7032-9907
OpenAlex ID: A5087616611
Cognitive function in amyotrophic lateral sclerosis: a cross-sectional and prospective pragmatic clinical study with review of the literature
2023 · Adamantios Katerelos, Panagiotis Alexopoulos, et al. · Neurological Sciences · 10
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Novel Hemizygous Missense Variant of Spermine Synthase (SMS) Gene Causes Snyder-Robinson Syndrome in a Four-Year-Old Boy
2021 · Stella Mouskou, Adamantios Katerelos, et al. · Molecular Syndromology · 8
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Growth Hormone Deficiency due to p.(Gln467Argfs*64) Mutation in the ARID1B Gene in a Girl with Coffin-Siris Syndrome
2022 · Stella Mouskou, Sofia Leka-Emiri, et al. · Molecular Syndromology · 3
Genetic Neuromuscular Diseases
2024 · Adamantios Katerelos · IntechOpen eBooks · 2
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Pharmacoresistant epilepsy associated with mutations in the KCNB1 and RELN genes. A case report
2020 · Adamantios Katerelos, Nikolaos Zagkos, et al. · Journal of Epileptology · 2
The Role of Neurolinguistics in Teaching Greek as a Second Language:
2025 · Amalia Moumouri, Adamantios Katerelos · INTERNATIONAL JOURNAL OF LANGUAGE TEACHING AND EDUCATION · 1
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Correction to: Cognitive function in amyotrophic lateral sclerosis: a cross‑sectional and prospective pragmatic clinical study with review of the literature
2024 · Adamantios Katerelos, Panagiotis Alexopoulos, et al. · Neurological Sciences · 1
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VGKC-Complex Antibody Positivity and Reversible Basal Ganglia Lesions in a Child with FIRES
2026 · Adamantios Katerelos, Ioanna Kermelioti, et al. · Journal of Pediatric Neurosciences
Seizures and Epilepsy in Children With SARS-CoV-2 Infection: Clinical Phenotypes, Mechanisms, and Long-Term Outcomes
2026 · Katerelos Adamantios · Journal of Neurology Research
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Infant microglial programming as the earliest determinant of brain aging: A roadmap for microglial age-trajectory mapping
2026 · Adamantios Katerelos · Aging advances.
Pediatric Facial Nerve Palsy: A Narrative Review of Etiology, Diagnosis, and Management
2026 · Adamantios Katerelos, Kalliopi Konstantinopoulou · Journal of Neurology Research
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A Novel Variant of Huwe1 Gene in a Female Infant With Syndrome Phenotype and Developmental Delay: a Case Report
2025 · Iliana Giannikopoulou, Eleni Stogiannidou, et al. · MNJ (Malang Neurology Journal)
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Juvenile Amyotrophic Lateral Sclerosis: a mini review of literature
2024 · Adamantios Katerelos · Journal of Medical Science
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Πλαγία μυατροφική σκλήρυνση και γνωσιακή διαταραχή
2024 · Αδαμάντιος Κατερέλος
Works count: 14
Citation count: 27
H-index: 3
I10-index: 1
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