TOLOMEO, Maria
TOLOMEO, Maria
A novel loss of function FLAD1 variant, causing riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD)
2018-01-01 Nochi, Z; Ryder, B; Tolomeo, M; Colella, M; Barile, M; Olsen, Rkj; Inbar‐feigenberg, M
A novel loss of function FLAD1 variant, causing riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD)
2018-01-01 Nochi, Z; Ryder, B; Tolomeo, M; Colella, M; Barile, M; Olsen, R K J; Inbar-Feigenberg, M
A Novel Truncating FLAD1 Variant, Causing Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in an 8-Year-Old Boy
2019-01-01 Ryder, B.; Tolomeo, M.; Nochi, Z.; Colella, M.; Barile, M.; Olsen, R. K.; Inbar-Feigenberg, M.
Adapting cellular riboflavin transport and metabolism in pancreatic ductal adenocarcinoma
2022-01-01 Nisco, Alessia; Squicciarino, Maria; Tolomeo, Maria; Tiago, Carvalho; DI MOLFETTA, Daria; Barile, Maria
Alteration of Flavin Cofactor Homeostasis in Human Neuromuscular Pathologies
2021-01-01 Tolomeo, Maria; Nisco, Alessia; Barile, Maria
Alteration of flavin homeostasis in neuromuscular disorders and cancer
2019-01-01 Tolomeo, Maria; Leone, Piero; Barile, Maria
Alteration of Riboflavin transporter expression in human cancer
2022-01-01 Nisco, Alessia; Tolomeo, Maria; Tiago, Carvalho; DI MOLFETTA, Daria; Barile, Maria
Altered expression of SLC52A members in human cancer
2018-01-01 Tolomeo, Maria; Loredana Defrancesco, Marianna; Esperti, Giordano; Barile, Maria
Bacterial production, characterization and protein modeling of a novel monofuctional isoform of FAD synthase in humans: an emergency protein?
2018-01-01 Leone, P.; Galluccio, M.; Barbiroli, A.; Eberini, I.; Tolomeo, M.; Vrenna, F.; Gianazza, E.; Iametti, S.; Bonomi, F.; Indiveri, C.; Barile, M.
Combined isobutyryl‐CoA and multiple acyl‐CoA dehydrogenase deficiency in a boy with altered riboflavin homeostasis
2022-01-01 Tummolo, Albina; Leone, Piero; Tolomeo, Maria; Solito, Rita; Mattiuzzo, Matteo; Lepri, Francesca Romana; Lorè, Tania; Cardinali, Roberta; De Giovanni, Donatella; Simonetti, Simonetta; Barile, Maria
Continuous and Discontinuous Approaches to Study FAD Synthesis and Degradation Catalyzed by Purified Recombinant FAD Synthase or Cellular Fractions
2021-01-01 Leone, Piero; Tolomeo, Maria; Barile, Maria
Development of Novel Experimental Models to Study Flavoproteome Alterations in Human Neuromuscular Diseases: The Effect of Rf Therapy
2020-01-01 Tolomeo, M.; Nisco, A.; Leone, P.; Barile, M.
FAD Synthase (FADS) localization and function in neuronal cell models: a possible involvement of FADS in the pathogenesis of neurodegenerative diseases.
2017-01-01 Difonzo, G.; Leone, P.; Tolomeo, M.; Defrancesco, M. L.; Damiano, M. T.; Giancaspero, T. A.; Colella, M.; Barile, M.
FAD synthase deficiency: a severe mitochondrial myopathy involving a secondary reduction of RFVT2 expression
2022-01-01 Barile, Maria; Tolomeo, Maria; Chimienti, Guglielmina; Lanza, Martina; Barbaro, Roberto; Latronico, Tiziana; Nisco, Alessia; Leone, Piero; Petrosillo, Giuseppe; Liuzzi, Grazia M.; Lezza, Angela M. S.; Colella, Matilde; Olsen, Rikke K.
FAD synthase deficiency: a severe mitochondrial myopathy searching for novel therapeutic strategies
2020-01-01 Barile, M.; Tolomeo, M.; Latronico, T.; Chimenti, G.; Leone, P.; Nisco, A.; Dipace, G.; Cardinale, M.; Lanza, M.; Barbaro, R.; Petrosillo, G.; Lezza, A. M. S.; Liuzzi, G. M.; Colella, M.; Olsen, R.
FAD SYNTHASE IN HUMAN MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY: INVESTIGATIONS IN S. CEREVISIAE
2018-01-01 Leone, Piero; Tolomeo, Maria; Giancaspero, TERESA ANNA; Bruni, Francesco; Oreb, Mislav; Roberti, Marina; Boles, Eckhard; Barile, Maria
Function and dysfunction of human riboflavin transporters
2019-01-01 Tolomeo, Maria; Console, Lara; Scalise, Mariafrancesca; Esperti, Giordano; Indiveri, Cesare; Barile, Maria
Functional characterization and homology modeling of a novel monofunctional isoform of human FAD synthase.
2017-01-01 Leone, P.; Galluccio, M.; Tolomeo, M.; Indiveri, C.; Barile, M.
Functional Study of the Human Riboflavin Transporter 2 Using Proteoliposomes System
2021-01-01 Console, Lara; Tolomeo, Maria; Indiveri, Cesare
Human riboflavin transporters in health and diseases
2019-01-01 Tolomeo, Maria; Console, Lara; Scalise, Mariafrancesca; Nisco, Alessia; Esperti, Giordano; Indiveri, Cesare; Barile, Maria
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A novel loss of function FLAD1 variant, causing riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD) | 1-gen-2018 | Nochi, Z; Ryder, B; Tolomeo, M; Colella, M; Barile, M; Olsen, Rkj; Inbar‐feigenberg, M | |
| A novel loss of function FLAD1 variant, causing riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD) | 1-gen-2018 | Nochi, Z; Ryder, B; Tolomeo, M; Colella, M; Barile, M; Olsen, R K J; Inbar-Feigenberg, M | |
| A Novel Truncating FLAD1 Variant, Causing Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in an 8-Year-Old Boy | 1-gen-2019 | Ryder, B.; Tolomeo, M.; Nochi, Z.; Colella, M.; Barile, M.; Olsen, R. K.; Inbar-Feigenberg, M. | |
| Adapting cellular riboflavin transport and metabolism in pancreatic ductal adenocarcinoma | 1-gen-2022 | Nisco, Alessia; Squicciarino, Maria; Tolomeo, Maria; Tiago, Carvalho; DI MOLFETTA, Daria; Barile, Maria | |
| Alteration of Flavin Cofactor Homeostasis in Human Neuromuscular Pathologies | 1-gen-2021 | Tolomeo, Maria; Nisco, Alessia; Barile, Maria | |
| Alteration of flavin homeostasis in neuromuscular disorders and cancer | 1-gen-2019 | Tolomeo, Maria; Leone, Piero; Barile, Maria | |
| Alteration of Riboflavin transporter expression in human cancer | 1-gen-2022 | Nisco, Alessia; Tolomeo, Maria; Tiago, Carvalho; DI MOLFETTA, Daria; Barile, Maria | |
| Altered expression of SLC52A members in human cancer | 1-gen-2018 | Tolomeo, Maria; Loredana Defrancesco, Marianna; Esperti, Giordano; Barile, Maria | |
| Bacterial production, characterization and protein modeling of a novel monofuctional isoform of FAD synthase in humans: an emergency protein? | 1-gen-2018 | Leone, P.; Galluccio, M.; Barbiroli, A.; Eberini, I.; Tolomeo, M.; Vrenna, F.; Gianazza, E.; Iametti, S.; Bonomi, F.; Indiveri, C.; Barile, M. | |
| Combined isobutyryl‐CoA and multiple acyl‐CoA dehydrogenase deficiency in a boy with altered riboflavin homeostasis | 1-gen-2022 | Tummolo, Albina; Leone, Piero; Tolomeo, Maria; Solito, Rita; Mattiuzzo, Matteo; Lepri, Francesca Romana; Lorè, Tania; Cardinali, Roberta; De Giovanni, Donatella; Simonetti, Simonetta; Barile, Maria | |
| Continuous and Discontinuous Approaches to Study FAD Synthesis and Degradation Catalyzed by Purified Recombinant FAD Synthase or Cellular Fractions | 1-gen-2021 | Leone, Piero; Tolomeo, Maria; Barile, Maria | |
| Development of Novel Experimental Models to Study Flavoproteome Alterations in Human Neuromuscular Diseases: The Effect of Rf Therapy | 1-gen-2020 | Tolomeo, M.; Nisco, A.; Leone, P.; Barile, M. | |
| FAD Synthase (FADS) localization and function in neuronal cell models: a possible involvement of FADS in the pathogenesis of neurodegenerative diseases. | 1-gen-2017 | Difonzo, G.; Leone, P.; Tolomeo, M.; Defrancesco, M. L.; Damiano, M. T.; Giancaspero, T. A.; Colella, M.; Barile, M. | |
| FAD synthase deficiency: a severe mitochondrial myopathy involving a secondary reduction of RFVT2 expression | 1-gen-2022 | Barile, Maria; Tolomeo, Maria; Chimienti, Guglielmina; Lanza, Martina; Barbaro, Roberto; Latronico, Tiziana; Nisco, Alessia; Leone, Piero; Petrosillo, Giuseppe; Liuzzi, Grazia M.; Lezza, Angela M. S.; Colella, Matilde; Olsen, Rikke K. | |
| FAD synthase deficiency: a severe mitochondrial myopathy searching for novel therapeutic strategies | 1-gen-2020 | Barile, M.; Tolomeo, M.; Latronico, T.; Chimenti, G.; Leone, P.; Nisco, A.; Dipace, G.; Cardinale, M.; Lanza, M.; Barbaro, R.; Petrosillo, G.; Lezza, A. M. S.; Liuzzi, G. M.; Colella, M.; Olsen, R. | |
| FAD SYNTHASE IN HUMAN MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY: INVESTIGATIONS IN S. CEREVISIAE | 1-gen-2018 | Leone, Piero; Tolomeo, Maria; Giancaspero, TERESA ANNA; Bruni, Francesco; Oreb, Mislav; Roberti, Marina; Boles, Eckhard; Barile, Maria | |
| Function and dysfunction of human riboflavin transporters | 1-gen-2019 | Tolomeo, Maria; Console, Lara; Scalise, Mariafrancesca; Esperti, Giordano; Indiveri, Cesare; Barile, Maria | |
| Functional characterization and homology modeling of a novel monofunctional isoform of human FAD synthase. | 1-gen-2017 | Leone, P.; Galluccio, M.; Tolomeo, M.; Indiveri, C.; Barile, M. | |
| Functional Study of the Human Riboflavin Transporter 2 Using Proteoliposomes System | 1-gen-2021 | Console, Lara; Tolomeo, Maria; Indiveri, Cesare | |
| Human riboflavin transporters in health and diseases | 1-gen-2019 | Tolomeo, Maria; Console, Lara; Scalise, Mariafrancesca; Nisco, Alessia; Esperti, Giordano; Indiveri, Cesare; Barile, Maria |