Lenzini L - Search Results

1

Nutrient Intake and Nutritional Status in Adult Patients with Inherited Metabolic Diseases Treated with Low-Protein Diets: A Review on Urea Cycle Disorders and Branched Chain Organic Acidemias.

Francini-Pesenti F, Gugelmo G, Lenzini L, Vitturi N. Francini-Pesenti F, et al. Among authors: lenzini l. Nutrients. 2020 Oct 29;12(11):3331. doi: 10.3390/nu12113331. Nutrients. 2020. PMID: 33138136 Free PMC article. Review.

2

SARS CoV2 infection in a young subject affected by arginosuccinate synthase deficiency: A case report of epilepsy worsening.

Vitturi N, Lenzini L, Francini-Pesenti F, Gugelmo G, Avogaro A. Vitturi N, et al. Among authors: lenzini l. Mol Genet Metab Rep. 2020 Dec 11;26:100698. doi: 10.1016/j.ymgmr.2020.100698. eCollection 2021 Mar. Mol Genet Metab Rep. 2020. PMID: 33354515 Free PMC article.

3

High prolactin levels in dihydropteridine reductase deficiency: A sign of therapy failure or additional pathology?

Vitturi N, Lenzini L, Luisi C, Carecchio M, Gugelmo G, Francini-Pesenti F, Avogaro A. Vitturi N, et al. Among authors: lenzini l. JIMD Rep. 2021 Jun 29;61(1):48-51. doi: 10.1002/jmd2.12236. eCollection 2021 Sep. JIMD Rep. 2021. PMID: 34485017 Free PMC article.

4

A novel MRPS34 gene mutation with combined OXPHOS deficiency in an adult patient with Leigh syndrome.

Lenzini L, Carecchio M, Iori E, Legati A, Lamantea E, Avogaro A, Vitturi N. Lenzini L, et al. Mol Genet Metab Rep. 2021 Dec 6;30:100830. doi: 10.1016/j.ymgmr.2021.100830. eCollection 2022 Mar. Mol Genet Metab Rep. 2021. PMID: 34938649 Free PMC article.

5

Anthropometrics, Dietary Intake and Body Composition in Urea Cycle Disorders and Branched Chain Organic Acidemias: A Case Study of 18 Adults on Low-Protein Diets.

Gugelmo G, Lenzini L, Francini-Pesenti F, Fasan I, Spinella P, Valentini R, Miraval A, Avogaro A, Vitturi N. Gugelmo G, et al. Among authors: lenzini l. Nutrients. 2022 Jan 21;14(3):467. doi: 10.3390/nu14030467. Nutrients. 2022. PMID: 35276826 Free PMC article.

6

Genetic Diagnosis in a Cohort of Adult Patients with Inherited Metabolic Diseases: A Single-Center Experience.

Lenzini L, Carraro G, Avogaro A, Vitturi N. Lenzini L, et al. Biomolecules. 2022 Jun 30;12(7):920. doi: 10.3390/biom12070920. Biomolecules. 2022. PMID: 35883476 Free PMC article.

7

Urine-Derived Epithelial Cells as a New Model to Study Renal Metabolic Phenotypes of Patients with Glycogen Storage Disease 1a.

Lenzini L, Iori E, Scannapieco F, Carraro G, Avogaro A, Vitturi N. Lenzini L, et al. Int J Mol Sci. 2022 Dec 23;24(1):232. doi: 10.3390/ijms24010232. Int J Mol Sci. 2022. PMID: 36613675 Free PMC article.

8

Gastrointestinal Manifestations and Low-FODMAP Protocol in a Cohort of Fabry Disease Adult Patients.

Gugelmo G, Vitturi N, Francini-Pesenti F, Fasan I, Lenzini L, Valentini R, Carraro G, Avogaro A, Spinella P. Gugelmo G, et al. Among authors: lenzini l. Nutrients. 2023 Jan 28;15(3):658. doi: 10.3390/nu15030658. Nutrients. 2023. PMID: 36771363 Free PMC article.

9

Understanding the Pathogenesis of Cardiac Complications in Patients with Propionic Acidemia and Exploring Therapeutic Alternatives for Those Who Are Not Eligible or Are Waiting for Liver Transplantation.

Maines E, Moretti M, Vitturi N, Gugelmo G, Fasan I, Lenzini L, Piccoli G, Gragnaniello V, Maiorana A, Soffiati M, Burlina A, Franceschi R. Maines E, et al. Among authors: lenzini l. Metabolites. 2023 Apr 16;13(4):563. doi: 10.3390/metabo13040563. Metabolites. 2023. PMID: 37110221 Free PMC article. Review.

10

Increased Soluble Interleukin 6 Receptors in Fabry Disease.

Lenzini L, Iori E, Vettore M, Gugelmo G, Radu C, Padoan A, Carraro G, Simioni P, Calò L, Avogaro A, Rossi GP, Vitturi N. Lenzini L, et al. J Clin Med. 2023 Dec 29;13(1):218. doi: 10.3390/jcm13010218. J Clin Med. 2023. PMID: 38202225 Free PMC article.

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