Publication White Matter Changes in Patients with Parkinson's Disease Carrying Small CGG Expansion FMR1 Alleles: A Pilot Study.
Publication Variant nonketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5.
Publication Variability of disease spectrum in children with liver phosphorylase kinase deficiency caused by mutations in the PHKG2 gene.
Publication Validation of relapse risk biomarkers for routine use in patients with juvenile idiopathic arthritis.
Publication The Effectiveness of Conjugate Haemophilus influenzae Type B Vaccine in The Gambia 14 Years After Introduction.
Publication Probiotics to prevent or treat excessive infant crying: systematic review and meta-analysis.
Publication Probiotic Effects on Late-onset Sepsis in Very Preterm Infants: A Randomized Controlled Trial.
