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Journal of Inherited Metabolic Disease|February 6, 2010
An overview of a cohort of South African patients with mitochondrial disordersIzelle Smuts, Roan Louw, Hanli du Toit, et al.Journal of Inherited Metabolic Disease|June 2, 2017
Hearing loss in children with Fabry diseaseE Suntjens, W A Dreschler, J Hess-Erga, et al.Journal of Inherited Metabolic Disease|July 29, 2018
Correction to: Medical and financial burden of acute intermittent porphyriaRochus A Neeleman, Margreet A E M Wagenmakers, Rita H Koole-Lesuis, et al.Journal of Inherited Metabolic Disease|July 20, 2018
Presynaptic disorders: a clinical and pathophysiological approach focused on the synaptic vesicleElisenda Cortès-Saladelafont, Noa Lipstein, Àngels García-CazorlaJournal of Inherited Metabolic Disease|April 21, 2018
Medical and financial burden of acute intermittent porphyriaRochus A Neeleman, Margreet A E M Wagenmakers, Rita H Koole-Lesuis, et al.Journal of Inherited Metabolic Disease|July 4, 2018
Development and characterization of an inducible mouse model for glycogen storage disease type IbFederica Raggi, Anna Livia Pissavino, Roberta Resaz, et al.Journal of Inherited Metabolic Disease|June 28, 2018
Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanismsLucia Abela, Manju A KurianJournal of Inherited Metabolic Disease|July 6, 2018
Cerebrospinal fluid monoamines, pterins, and folate in patients with mitochondrial diseases: systematic review and hospital experienceMarta Batllori, Marta Molero-Luis, Aida Ormazabal, et al.Journal of Inherited Metabolic Disease|July 15, 2018
Transcranial electrical stimulation (tES) mechanisms and its effects on cortical excitability and connectivityThomas Reed, Roi Cohen KadoshJournal of Inherited Metabolic Disease|January 20, 2010
Neuronopathic Gaucher disease: demographic and clinical features of 131 patients enrolled in the International Collaborative Gaucher Group Neurological Outcomes SubregistryAnna Tylki-Szymańska, Ashok Vellodi, Amal El-Beshlawy, et al.Pageof 429