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Moyamoya syndrome and neurofibromatosis type 1.
Vargiami E, Sapountzi E, Samakovitis D, Batzios S, Kyriazi M, Anastasiou A, Zafeiriou DI. Vargiami E, et al. Among authors: batzios s. Ital J Pediatr. 2014 Jun 21;40:59. doi: 10.1186/1824-7288-40-59. Ital J Pediatr. 2014. PMID: 24952383 Free PMC article.
Mutated SUCLG1 causes mislocalization of SUCLG2 protein, morphological alterations of mitochondria and an early-onset severe neurometabolic disorder.
Chinopoulos C, Batzios S, van den Heuvel LP, Rodenburg R, Smeets R, Waterham HR, Turkenburg M, Ruiter JP, Wanders RJA, Doczi J, Horvath G, Dobolyi A, Vargiami E, Wevers RA, Zafeiriou D. Chinopoulos C, et al. Among authors: batzios s. Mol Genet Metab. 2019 Jan;126(1):43-52. doi: 10.1016/j.ymgme.2018.11.009. Epub 2018 Nov 16. Mol Genet Metab. 2019. PMID: 30470562
A "sweet" hydrothorax in a child on peritoneal dialysis.
Gidaris D, Printza N, Batzios S, Belechri AM, Papachristou F. Gidaris D, et al. Among authors: batzios s. Hippokratia. 2011 Oct;15(4):358-60. Hippokratia. 2011. PMID: 24391421 Free PMC article.
38 results