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In vitro study of uptake and synthesis of creatine and its precursors by cerebellar granule cells and astrocytes suggests some hypotheses on the physiopathology of the inherited disorders of creatine metabolism.
Carducci C, Carducci C, Santagata S, Adriano E, Artiola C, Thellung S, Gatta E, Robello M, Florio T, Antonozzi I, Leuzzi V, Balestrino M. Carducci C, et al. Among authors: artiola c. BMC Neurosci. 2012 Apr 26;13:41. doi: 10.1186/1471-2202-13-41. BMC Neurosci. 2012. PMID: 22536786 Free PMC article.
The pathogenesis of the white matter abnormalities in phenylketonuria. A multimodal 3.0 tesla MRI and magnetic resonance spectroscopy (1H MRS) study.
Leuzzi V, Tosetti M, Montanaro D, Carducci C, Artiola C, Carducci C, Antonozzi I, Burroni M, Carnevale F, Chiarotti F, Popolizio T, Giannatempo GM, D'Alesio V, Scarabino T. Leuzzi V, et al. Among authors: artiola c. J Inherit Metab Dis. 2007 Apr;30(2):209-16. doi: 10.1007/s10545-006-0399-4. Epub 2007 Jan 23. J Inherit Metab Dis. 2007. PMID: 17245558
Tyrosine hydroxylase deficiency presenting with a biphasic clinical course.
Giovanniello T, Leuzzi V, Carducci C, Carducci C, Sabato ML, Artiola C, Santagata S, Pozzessere S, Antonozzi I. Giovanniello T, et al. Among authors: artiola c. Neuropediatrics. 2007 Aug;38(4):213-5. doi: 10.1055/s-2007-991151. Neuropediatrics. 2007. PMID: 18058633
Report of two never treated adult sisters with aromatic L-amino Acid decarboxylase deficiency: a portrait of the natural history of the disease or an expanding phenotype?
Leuzzi V, Mastrangelo M, Polizzi A, Artiola C, van Kuilenburg AB, Carducci C, Ruggieri M, Barone R, Tavazzi B, Abeling NG, Zoetekouw L, Sofia V, Zappia M, Carducci C. Leuzzi V, et al. Among authors: artiola c. JIMD Rep. 2015;15:39-45. doi: 10.1007/8904_2014_295. Epub 2014 May 1. JIMD Rep. 2015. PMID: 24788355 Free PMC article.
11 results