Carducci C - Search Results

1

New findings about neuropathological outcomes in the PKU mouse throughout lifespan.

Bregalda A, Carducci C, Pascucci T, Ambrogini P, Sartini S, Pierigè F, di Carlo E, Fiori E, Ielpo D, Pagliarini M, Leuzzi V, Magnani M, Rossi L. Bregalda A, et al. Among authors: carducci c. Mol Genet Metab. 2024 Sep-Oct;143(1-2):108543. doi: 10.1016/j.ymgme.2024.108543. Epub 2024 Jul 19. Mol Genet Metab. 2024. PMID: 39047302

2

A new therapy prevents intellectual disability in mouse with phenylketonuria.

Pascucci T, Rossi L, Colamartino M, Gabucci C, Carducci C, Valzania A, Sasso V, Bigini N, Pierigè F, Viscomi MT, Ventura R, Cabib S, Magnani M, Puglisi-Allegra S, Leuzzi V. Pascucci T, et al. Among authors: carducci c. Mol Genet Metab. 2018 May;124(1):39-49. doi: 10.1016/j.ymgme.2018.03.009. Epub 2018 Apr 7. Mol Genet Metab. 2018. PMID: 29661557

3

Myelin basic protein recovery during PKU mice lifespan and the potential role of microRNAs on its regulation.

Bregalda A, Carducci C, Viscomi MT, Pierigè F, Biagiotti S, Menotta M, Biancucci F, Pascucci T, Leuzzi V, Magnani M, Rossi L. Bregalda A, et al. Among authors: carducci c. Neurobiol Dis. 2023 May;180:106093. doi: 10.1016/j.nbd.2023.106093. Epub 2023 Mar 21. Neurobiol Dis. 2023. PMID: 36948260 Free article.

4

Erythrocyte-mediated delivery of phenylalanine ammonia lyase for the treatment of phenylketonuria in BTBR-Pah(enu2) mice.

Rossi L, Pierigè F, Carducci C, Gabucci C, Pascucci T, Canonico B, Bell SM, Fitzpatrick PA, Leuzzi V, Magnani M. Rossi L, et al. Among authors: carducci c. J Control Release. 2014 Nov 28;194:37-44. doi: 10.1016/j.jconrel.2014.08.012. Epub 2014 Aug 23. J Control Release. 2014. PMID: 25151978 Free article.

5

Neurocognitive and neuroimaging outcome of early treated young adult PKU patients: A longitudinal study.

Nardecchia F, Manti F, Chiarotti F, Carducci C, Carducci C, Leuzzi V. Nardecchia F, et al. Among authors: carducci c. Mol Genet Metab. 2015 Jun-Jul;115(2-3):84-90. doi: 10.1016/j.ymgme.2015.04.003. Epub 2015 Apr 29. Mol Genet Metab. 2015. PMID: 25952249

6

Urine sepiapterin excretion as a new diagnostic marker for sepiapterin reductase deficiency.

Carducci C, Santagata S, Friedman J, Pasquini E, Carducci C, Tolve M, Angeloni A, Leuzzi V. Carducci C, et al. Mol Genet Metab. 2015 Aug;115(4):157-60. doi: 10.1016/j.ymgme.2015.06.009. Epub 2015 Jun 25. Mol Genet Metab. 2015. PMID: 26123188

7

Clinical characterization of tremor in patients with phenylketonuria.

Nardecchia F, Manti F, De Leo S, Carducci C, Leuzzi V. Nardecchia F, et al. Among authors: carducci c. Mol Genet Metab. 2019 Sep-Oct;128(1-2):53-56. doi: 10.1016/j.ymgme.2019.05.017. Epub 2019 Jun 3. Mol Genet Metab. 2019. PMID: 31208951

8

Multiple sclerosis and intracellular cobalamin defect (MMACHC/PRDX1) comorbidity in a young male.

Pollini L, Tolve M, Nardecchia F, Galosi S, Carducci C, di Carlo E, Carducci C, Leuzzi V. Pollini L, et al. Among authors: carducci c. Mol Genet Metab Rep. 2020 Jan 7;22:100560. doi: 10.1016/j.ymgmr.2019.100560. eCollection 2020 Mar. Mol Genet Metab Rep. 2020. PMID: 32099815 Free PMC article.

9

Intellectual Disability and Brain Creatine Deficit: Phenotyping of the Genetic Mouse Model for GAMT Deficiency.

Rossi L, Nardecchia F, Pierigè F, Ventura R, Carducci C, Leuzzi V, Magnani M, Cabib S, Pascucci T. Rossi L, et al. Among authors: carducci c. Genes (Basel). 2021 Aug 2;12(8):1201. doi: 10.3390/genes12081201. Genes (Basel). 2021. PMID: 34440375 Free PMC article. Review.

10

Executive functioning, adaptive skills, emotional and behavioral profile: A comparison between autism spectrum disorder and phenylketonuria.

Trimarco B, Manti F, Nardecchia F, Melogno S, Testa M, Meledandri G, Carducci C, Penge R, Leuzzi V. Trimarco B, et al. Among authors: carducci c. Mol Genet Metab Rep. 2020 Mar 9;23:100577. doi: 10.1016/j.ymgmr.2020.100577. eCollection 2020 Jun. Mol Genet Metab Rep. 2020. PMID: 32181141 Free PMC article.

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