Blood–brain barrier structure and function and the challenges for CNS drug delivery - Abbott - 2013 - Journal of Inherited Metabolic Disease - Wiley Online Library
Gajja Salomons - Scientific Advisory Board @ Lumos Pharma - Crunchbase Person Profile
Symposium Updates On Neurometabolic Disorders
PDF) D-2-hydroxyglutaric aciduria Type I: Functional analysis of D2HGDH missense variants
Bi-allelic Mutations in EPRS, Encoding the Glutamyl-Prolyl-Aminoacyl-tRNA Synthetase, Cause a Hypomyelinating Leukodystrophy
Declaration of competence Laboratory Genetic Metabolic Diseases (lab GMD), Amsterdam UMC
Gajja Salomons(Amsterdam, The Netherlands) | Winglet Community
III Disorders of Mitochondrial Energy Metabolism
1H] Magnetic Resonance Spectroscopy of Urine: Diagnosis of a Guanidinoacetate Methyl Transferase Deficiency Case
THE SOCIETY FOR THE STUDY INBORN ERRORS OF METABOLISM
Advisors - Yasho's Leukodystrophy Foundation
SSIEM - Prof Gajja S Salomons, PhD
Amazon.co.jp: Creatine and Creatine Kinase in Health and Disease: From Cell Deconstruction to System Reconstruction (Subcellular Biochemistry) : Salomons, Gajja S., Wyss, Markus: Foreign Language Books
Diana Neele on Twitter: "Wat een mooie oratie en gezellig feest! prof Gajja Salomons gefeliciteerd! @VUmcAmsterdam http://t.co/8UxGzOH4f6" / Twitter
PDF) Clinical and molecular characteristics of two transaldolase-deficient patients
High Prevalence of SLC6A8 Deficiency in X-Linked Mental Retardation - ppt download
Genotypic diversity and phenotypic spectrum of infantile liver failure syndrome type 1 due to variants in LARS1
