Research challenges in central nervous system manifestations of inborn errors of metabolism
Year: 2010
Type: article
Authors: P.I. Dickson, A.R. Pariser, S.C. Groft, R.W. Ishihara, D.E. McNeil, D. Tagle, D.J. Griebel, S.G. Kaler, J.W. Mink, E.G. Shapiro
Institutions: University of California, Los Angeles, The Lundquist Institute, United States Food and Drug Administration, Center for Drug Evaluation and Research, National Institutes of Health, National Institute of Neurological Disorders and Stroke, Eunice Kennedy Shriver National Institute of Child Health and Human Development, University of Rochester Medicine, University of Rochester, University of Minnesota
Language: English
Subfield: Clinical Biochemistry
Domain: Life Sciences
Open Access status: green
Awards: Inherited Disorders of Copper Transport, Rare Diseases CRC: Urea Cycle Disorders, Newborn Screening for Adrenoleukodystrophy, Clinical and Neuropsychological Investigations in Batten Disease, Rare Diseases Clinical Research Consortia (RDCRC) for the Rare Diseases Clinical Research Network (RDCRN) (U54 Clinical Trial Optional), G5201875703, G5325585467, G5506619874, Lysosomal Disease Network, G5869032330, General Clinical Research Center, Intrathecal enzyme therapy for mucopolysaccharidosis I, G8854930239
OpenAlex ID: W1964396240