Verschuiving zegevierend operator gajja salomons Bezienswaardigheden bekijken vaak Klik
Bi-allelic Mutations in EPRS, Encoding the Glutamyl-Prolyl-Aminoacyl-tRNA Synthetase, Cause a Hypomyelinating Leukodystrophy
1H] Magnetic Resonance Spectroscopy of Urine: Diagnosis of a Guanidinoacetate Methyl Transferase Deficiency Case
The Journal of Inherited Metabolic Disease on Twitter: "Gajja Salomons #SSIEM Chairman speaking at #ICIEM2017 #Rio on treatable disorders of solute carriers SLCs https://t.co/bIWamF7cz8" / Twitter
A new case of GABA transaminase deficiency facilitated by proton MR spectroscopy
Diana Neele on Twitter: "Wat een mooie oratie en gezellig feest! prof Gajja Salomons gefeliciteerd! @VUmcAmsterdam http://t.co/8UxGzOH4f6" / Twitter
GPE aims to improve transparency, monitoring of education funding pledges | Devex
PDF) Clinical and molecular characteristics of two transaldolase-deficient patients
Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms.
Advisors - Yasho's Leukodystrophy Foundation
Gajja Salomons(Amsterdam, The Netherlands) | Winglet Community
PDF) D-2-hydroxyglutaric aciduria Type I: Functional analysis of D2HGDH missense variants
Scientific Medical Advisory Board (SMAB) – Association for Creatine Deficiencies
Creatine and Creatine Kinase in Health and Disease: Salomons, Gajja S., Wyss, Markus: 9781402064852: Genetics: Amazon Canada
AGEM research board
Progress in understanding 2-hydroxyglutaric acidurias – ScienceOpen
Blood–brain barrier structure and function and the challenges for CNS drug delivery - Abbott - 2013 - Journal of Inherited Metabolic Disease - Wiley Online Library
Advisors - Yasho's Leukodystrophy Foundation
Programme du Symposium Rotterdam 6 & 7 septembre 2019 Salle De Doelen
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