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Early-onset LBSL: how severe does it get?
Steenweg ME, van Berge L, van Berkel CG, de Coo IF, Temple IK, Brockmann K, Mendonça CI, Vojta S, Kolk A, Peck D, Carr L, Uziel G, Feigenbaum A, Blaser S, Scheper GC, van der Knaap MS. Steenweg ME, et al. Among authors: feigenbaum a. Neuropediatrics. 2012 Dec;43(6):332-8. doi: 10.1055/s-0032-1329395. Epub 2012 Oct 12. Neuropediatrics. 2012. PMID: 23065766
Hypomyelination with atrophy of the basal ganglia and cerebellum: follow-up and pathology.
van der Knaap MS, Linnankivi T, Paetau A, Feigenbaum A, Wakusawa K, Haginoya K, Köhler W, Henneke M, Dinopoulos A, Grattan-Smith P, Brockmann K, Schiffmann R, Blaser S. van der Knaap MS, et al. Among authors: feigenbaum a. Neurology. 2007 Jul 10;69(2):166-71. doi: 10.1212/01.wnl.0000265592.74483.a6. Neurology. 2007. PMID: 17620549
Genotype-phenotype correlation in vanishing white matter disease.
van der Lei HD, van Berkel CG, van Wieringen WN, Brenner C, Feigenbaum A, Mercimek-Mahmutoglu S, Philippart M, Tatli B, Wassmer E, Scheper GC, van der Knaap MS. van der Lei HD, et al. Among authors: feigenbaum a. Neurology. 2010 Oct 26;75(17):1555-9. doi: 10.1212/WNL.0b013e3181f962ae. Neurology. 2010. PMID: 20975056
Natural History of Vanishing White Matter.
Hamilton EMC, van der Lei HDW, Vermeulen G, Gerver JAM, Lourenço CM, Naidu S, Mierzewska H, Gemke RJBJ, de Vet HCW, Uitdehaag BMJ, Lissenberg-Witte BI; VWM Research Group; van der Knaap MS. Hamilton EMC, et al. Ann Neurol. 2018 Aug;84(2):274-288. doi: 10.1002/ana.25287. Epub 2018 Sep 6. Ann Neurol. 2018. PMID: 30014503 Free PMC article.
Atypical phenotype in a boy with a maple syrup urine disease.
Ben-Omran TI, Blaser S, Phillips H, Callahan J, Feigenbaum A. Ben-Omran TI, et al. Among authors: feigenbaum a. J Inherit Metab Dis. 2006 Feb;29(1):195-200. doi: 10.1007/s10545-006-0224-0. J Inherit Metab Dis. 2006. PMID: 16601891
216 results