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Methods in Molecular Biology (Clifton, N.J.)|January 6, 2011
Analysis of organic acids and acylglycines for the diagnosis of related inborn errors of metabolism by GC- and HPLC-MSGiancarlo la Marca, Cristiano RizzoMetabolites|August 28, 2024
Propionic Acidemia, Methylmalonic Acidemia, and Cobalamin C Deficiency: Comparison of Untargeted Metabolomic ProfilesAnna Sidorina, Giulio Catesini, Elisa Sacchetti, et al.Journal of Neuroscience Methods|April 3, 2007
Off-line removal of TMS-induced artifacts on human electroencephalography by Kalman filterFabio Morbidi, Andrea Garulli, Domenico Prattichizzo, et al.Pediatric Research|January 28, 2006
Impaired activity of the gamma-glutamyl cycle in nephropathic cystinosis fibroblastsLiliana Mannucci, Anna Pastore, Cristiano Rizzo, et al.Nutrients|October 16, 2024
Nutritional Counseling and Mediterranean Diet in Adrenoleukodystrophy: A Real-Life ExperienceMaria Rita Spreghini, Nicoletta Gianni, Tommaso Todisco, et al.Investigacion Clinica|April 17, 2007
[Diagnosis and treatment of methylmalonic aciduria: a case report]Antonieta Mahfoud, Carmen L Domínguez, Analy Pérez, et al.Endocrinology, Diabetes & Metabolism Case Reports|May 20, 2021
ABCD1 gene mutation in an Italian family with X-linkedadrenoleukodystrophy: case seriesAngelika Mohn, Nella Polidori, Chiara Aiello, et al.Journal of Lipid Research|January 7, 2016
Evaluation of plasma cholestane-3β,5α,6β-triol and 7-ketocholesterol in inherited disorders related to cholesterol metabolismSara Boenzi, Federica Deodato, Roberta Taurisano, et al.Nutrition (Burbank, Los Angeles County, Calif.)|July 3, 2014
Acute thiamine deficiency and refeeding syndrome: Similar findings but different pathogenesisArianna Maiorana, Gianluca Vergine, Valentina Coletti, et al.Journal of Lipid Research|December 22, 2025
New Multiplex LC-MS/MS Method for lipid biomarker Analysis of Inherited Neurodegenerative Metabolic DiseasesAnna Sidorina, Giulio Catesini, Federica Deodato, et al.Pageof 5