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Glutaric aciduria type I: pathomechanisms of neurodegeneration.
Ullrich K, Flott-Rahmel B, Schluff P, Musshoff U, Das A, Lücke T, Steinfeld R, Christensen E, Jakobs C, Ludolph A, Neu A, Röper R. Ullrich K, et al. Among authors: neu a. J Inherit Metab Dis. 1999 Jun;22(4):392-403. doi: 10.1023/a:1005595921323. J Inherit Metab Dis. 1999. PMID: 10407776
L-arginine:glycine amidinotransferase deficiency protects from metabolic syndrome.
Choe CU, Nabuurs C, Stockebrand MC, Neu A, Nunes P, Morellini F, Sauter K, Schillemeit S, Hermans-Borgmeyer I, Marescau B, Heerschap A, Isbrandt D. Choe CU, et al. Among authors: neu a. Hum Mol Genet. 2013 Jan 1;22(1):110-23. doi: 10.1093/hmg/dds407. Epub 2012 Oct 1. Hum Mol Genet. 2013. PMID: 23026748
Muscle phenotype of AGAT- and GAMT-deficient mice after simvastatin exposure.
Sasani A, Hornig S, Grzybowski R, Cordts K, Hanff E, Tsikas D, Böger R, Gerloff C, Isbrandt D, Neu A, Schwedhelm E, Choe CU. Sasani A, et al. Among authors: neu a. Amino Acids. 2020 Jan;52(1):73-85. doi: 10.1007/s00726-019-02812-4. Epub 2019 Dec 18. Amino Acids. 2020. PMID: 31853708
305 results