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Neuropediatrics

JournalCitation impact & published research

Neuropediatrics is a journal indexed in ScholarIQ from OpenAlex. ScholarIQ records 7,746 works, 79,891 citations and an h-index of 100.

7,746
Works
79,891
Citations
100
h-index

What are the most-cited papers on Neuropediatrics?

ScholarIQmost cited works
Earliest Clinical Manifestations and Natural History of Neurofibromatosis Type 2 (NF2) in Childhood: A Study of 24 Patients
Martino Ruggieri, Paola Iannetti, Agata Polizzi, Ignazio La Mantia, Alberto Spalice, O. Giliberto, Nunzio Platania, A. L. Gabriele, Valentina Erminia Albanese, Piero Pavone
Neuropediatrics. 2005139 Citations
Limited Knowledge of Tourette Syndrome Causes Delay in Diagnosis
Nanette Mol Debes, Helle Hjalgrim, Liselotte Skov
Neuropediatrics. 200875 Citations
Effects of Oral Creatine Supplementation in a Patient with MELAS Phenotype and Associated Nephropathy
Nina Barišić, Günther Bernert, O. Ipsiroglu, Carmen Stromberger, T. Müller, Stephan Gruber, D. Prayer, Ewald Moser, Reginald E. Bittner, S. Stöckler-Ipsiroglu
Neuropediatrics. 200265 Citations
Chilblains as a Diagnostic Sign of Aicardi-Goutières Syndrome
Ghada M. H. Abdel‐Salam, Ghada El‐Kamah, Gillian Rice, Mohamed El‐Darouti, Hannah Gornall, Marcin Szynkiewicz, FRANÇOIS AYMARD, Maha S. Zaki, Alice Abdel Aleem, Pierre Lebon, Yanick J. Crow
Neuropediatrics. 201039 Citations
Novel MECR Mutation in Childhood-Onset Dystonia, Optic Atrophy, and Basal Ganglia Signal Abnormalities
Orhan Görükmez, Özlem Görükmez, Cengiz Havalı
Neuropediatrics. 201916 Citations

Related on ScholarIQ

Earliest Clinical Manifestations and Natural History of Neurofibromatosis Type 2 (NF2) in Childhood: A Study of 24 Patients
Paper
Limited Knowledge of Tourette Syndrome Causes Delay in Diagnosis
Paper
Effects of Oral Creatine Supplementation in a Patient with MELAS Phenotype and Associated Nephropathy
Paper
Chilblains as a Diagnostic Sign of Aicardi-Goutières Syndrome
Paper
Novel MECR Mutation in Childhood-Onset Dystonia, Optic Atrophy, and Basal Ganglia Signal Abnormalities
Paper
Fenfluramine Treatment Improves Everyday Executive Functioning in Patients with Lennox-Gastaut Syndrome: Analysis from a Phase 3 Clinical Trial
Paper
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