Scientific Committee – SSIEM Virtual Symposium
Gajja Salomons - Scientific Advisory Board @ Lumos Pharma - Crunchbase Person Profile
CERTIFICATE OF ATTENDANCE
Diana Neele on Twitter: "Wat een mooie oratie en gezellig feest! prof Gajja Salomons gefeliciteerd! @VUmcAmsterdam http://t.co/8UxGzOH4f6" / Twitter
Gallbladder and the risk of polyps and carcinoma in metachromatic leukodystrophy
Genotypic diversity and phenotypic spectrum of infantile liver failure syndrome type 1 due to variants in LARS1
Progress in understanding 2-hydroxyglutaric acidurias – ScienceOpen
Symposium Updates On Neurometabolic Disorders
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
Are cerebral creatine deficiency syndromes on the radar screen?
GPE aims to improve transparency, monitoring of education funding pledges | Devex
SSIEM - Prof Gajja S Salomons, PhD
High Prevalence of SLC6A8 Deficiency in X-Linked Mental Retardation - ppt download
Advisors - Yasho's Leukodystrophy Foundation
A new case of GABA transaminase deficiency facilitated by proton MR spectroscopy
Creatine and Creatine Kinase in Health and Disease: Salomons, Gajja S., Wyss, Markus: 9781402064852: Genetics: Amazon Canada
Bi-allelic Mutations in EPRS, Encoding the Glutamyl-Prolyl-Aminoacyl-tRNA Synthetase, Cause a Hypomyelinating Leukodystrophy
CHAPTER 8 CEREBRAL CREATINE DEFICIENCY SYNDROMES: CLINICAL ASPECTS, TREATMENT AND PATHOPHYSIOLOGY
Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms.
Scientific Medical Advisory Board (SMAB) – Association for Creatine Deficiencies
Heterozygous Variants in the Mechanosensitive Ion Channel TMEM63A Result in Transient Hypomyelination during Infancy
1H] Magnetic Resonance Spectroscopy of Urine: Diagnosis of a Guanidinoacetate Methyl Transferase Deficiency Case
