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Multiple Sclerosis (Houndmills, Basingstoke, England)|June 22, 2012
Differences and similarities in the evolution of morphologic brain abnormalities between paediatric and adult-onset multiple sclerosisA Pichler, C Enzinger, S Fuchs, et al.
Neurology|December 21, 2007
GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like diseaseM Henneke, P Combes, S Diekmann, et al.
Brain : a Journal of Neurology|May 23, 2002
Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder?P De Jonghe, M Auer-Grumbach, J Irobi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 27, 2016
Epileptic phenotypes, electroclinical features and clinical characteristics in 17 children with anti-NMDAR encephalitisE Haberlandt, M Ensslen, U Gruber-Sedlmayr, et al.
Neuropediatrics|May 28, 2008
Two novel mutations in the GDAP1 and PRX genes in early onset Charcot-Marie-Tooth syndromeM Auer-Grumbach, C Fischer, L Papić, et al.
Neuropediatrics|June 1, 1996
Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiencyG F Hoffmann, S Athanassopoulos, A B Burlina, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 18, 2018
Pyridoxine dependent epilepsy: Is late onset a predictor for favorable outcome?R L P de Rooy, F J Halbertsma, E A Struijs, et al.
Journal of Inherited Metabolic Disease|May 20, 2009
Treatment recommendations in long-chain fatty acid oxidation defects: consensus from a workshopU Spiekerkoetter, M Lindner, R Santer, et al.
Journal of Inherited Metabolic Disease|April 29, 2009
Management and outcome in 75 individuals with long-chain fatty acid oxidation defects: results from a workshopU Spiekerkoetter, M Lindner, R Santer, et al.
Journal of Inherited Metabolic Disease|December 21, 2014
Clinical onset and course, response to treatment and outcome in 24 patients with the cblE or cblG remethylation defect complemented by genetic and in vitro enzyme study dataM Huemer, C Bürer, P Ješina, et al.
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