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Neuropediatrics|May 31, 2003
Diffusion-weighted MRI in severe neonatal hypoxic ischaemia: the white cerebrumR J Vermeulen, W P F Fetter, L Hendrikx, et al.
Neuropediatrics|April 12, 2003
Neurological presentation in pediatric patients with congenital disorders of glycosylation type IaE Miossec-Chauvet, Y Mikaeloff, D Heron, et al.
Neuropediatrics|April 12, 2003
Human mitochondrial complex I deficiency: investigating transcriptional responses by microarrayF H van der Westhuizen, L P van den Heuvel, R Smeets, et al.
Neuropediatrics|May 1, 1987
Multiple system atrophy with retinal degeneration in a young childM Nishimura, T Mito, S Takashima, et al.
Neuropediatrics|December 1, 2021
Clinical and Genetic Aspects of Juvenile Onset Pompe DiseaseJohanna Holzwarth, Nadja Minopoli, Charlotte Pfrimmer, et al.
Neuropediatrics|December 1, 2021
Alternating Hemiplegia of Childhood in a Child Harboring a Novel TBC1D24 Mutation: Case Report and Literature ReviewRamona Cordani, Livia Pisciotta, Maria Margherita Mancardi, et al.
Neuropediatrics|December 1, 2021
Aphasia and a Dual-Stream Language Model in a 4-Year-Old Female with Landau-Kleffner SyndromeMichiko Kawai, Yuichi Abe, Masato Yumoto, et al.
Neuropediatrics|December 1, 2021
Spinal Nerve Roots Abnormalities on MRI in a Child with SURF1 Mitochondrial DiseaseAlfonso Rubino, Giorgia Bruno, Federica Mazio, et al.
Neuropediatrics|November 20, 2018
Diagnostic Pathway to Nonsense Mutation Dystrophinopathy: A Tertiary-Center, Retrospective ExperienceDidem Ardıçlı, Goknur Haliloğlu, Mehmet Alikaşifoğlu, et al.
Neuropediatrics|April 3, 2019
A De Novo Dominant Negative Mutation in DNM1L Causes Sudden Onset Status Epilepticus with Subsequent Epileptic EncephalopathyS J Schmid, M Wagner, C Goetz, et al.
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