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Evidence for treatable inborn errors of metabolism in a cohort of 187 Greek patients with autism spectrum disorder (ASD).
Spilioti M, Evangeliou AE, Tramma D, Theodoridou Z, Metaxas S, Michailidi E, Bonti E, Frysira H, Haidopoulou A, Asprangathou D, Tsalkidis AJ, Kardaras P, Wevers RA, Jakobs C, Gibson KM. Spilioti M, et al. Among authors: wevers ra. Front Hum Neurosci. 2013 Dec 24;7:858. doi: 10.3389/fnhum.2013.00858. eCollection 2013. Front Hum Neurosci. 2013. PMID: 24399946 Free PMC article.
Leukoencephalopathy associated with a disturbance in the metabolism of polyols.
van der Knaap MS, Wevers RA, Struys EA, Verhoeven NM, Pouwels PJ, Engelke UF, Feikema W, Valk J, Jakobs C. van der Knaap MS, et al. Among authors: wevers ra. Ann Neurol. 1999 Dec;46(6):925-8. doi: 10.1002/1531-8249(199912)46:6<925::aid-ana18>3.0.co;2-j. Ann Neurol. 1999. PMID: 10589548
Clinical significance of low cobalamin levels in older hospital patients.
van Asselt DZ, Blom HJ, Zuiderent R, Wevers RA, Jakobs C, van den Broek WJ, Lamers CB, Corstens FH, Hoefnagels WH. van Asselt DZ, et al. Among authors: wevers ra. Neth J Med. 2000 Aug;57(2):41-9. doi: 10.1016/s0300-2977(00)00048-6. Neth J Med. 2000. PMID: 10924940
Selective screening for inborn errors of metabolism: the primary care-based model in rural Crete.
Evangeliou A, Lionis C, Michailidou H, Spilioti M, Kanitsakis A, Nikitakis P, Drakonakis N, Giannakopoulou C, Sbyrakis S, Sewell AC, Boehles HJ, Smeitink J, Wevers RA. Evangeliou A, et al. Among authors: wevers ra. J Inherit Metab Dis. 2001 Dec;24(8):877-80. doi: 10.1023/a:1013904627537. J Inherit Metab Dis. 2001. PMID: 11916324 No abstract available.
Cardiac manifestations of inborn errors of metabolism.
Evangeliou A, Papadopoulou-Legbelou K, Daphnis E, Ganotakis E, Vavouranakis I, Michailidou H, Hitoglou-Makedou A, Nicolaidou P, Wevers R, Varlamis G. Evangeliou A, et al. Minerva Pediatr. 2007 Jun;59(3):215-8. Minerva Pediatr. 2007. PMID: 17519866
Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies.
Lefeber DJ, Schönberger J, Morava E, Guillard M, Huyben KM, Verrijp K, Grafakou O, Evangeliou A, Preijers FW, Manta P, Yildiz J, Grünewald S, Spilioti M, van den Elzen C, Klein D, Hess D, Ashida H, Hofsteenge J, Maeda Y, van den Heuvel L, Lammens M, Lehle L, Wevers RA. Lefeber DJ, et al. Among authors: wevers ra. Am J Hum Genet. 2009 Jul;85(1):76-86. doi: 10.1016/j.ajhg.2009.06.006. Epub 2009 Jul 2. Am J Hum Genet. 2009. PMID: 19576565 Free PMC article.
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