Rosato BE - Search Results

1

Uridine treatment normalizes the congenital dyserythropoietic anemia type II-like hematological phenotype in a patient with homozygous mutation in the CAD gene.

Russo R, Marra R, Andolfo I, Manna F, De Rosa G, Rosato BE, Radhakrishnan K, Fahey M, Iolascon A. Russo R, et al. Among authors: rosato be. Am J Hematol. 2020 Nov;95(11):1423-1426. doi: 10.1002/ajh.25946. Epub 2020 Aug 19. Am J Hematol. 2020. PMID: 32720728 Free article. No abstract available.

2

PIEZO1-R1864H rare variant accounts for a genetic phenotype-modifier role in dehydrated hereditary stomatocytosis.

Andolfo I, Manna F, De Rosa G, Rosato BE, Gambale A, Tomaiuolo G, Carciati A, Marra R, De Franceschi L, Iolascon A, Russo R. Andolfo I, et al. Among authors: rosato be. Haematologica. 2018 Mar;103(3):e94-e97. doi: 10.3324/haematol.2017.180687. Epub 2017 Nov 30. Haematologica. 2018. PMID: 29191841 Free PMC article. No abstract available.

3

Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias.

Russo R, Andolfo I, Manna F, Gambale A, Marra R, Rosato BE, Caforio P, Pinto V, Pignataro P, Radhakrishnan K, Unal S, Tomaiuolo G, Forni GL, Iolascon A. Russo R, et al. Among authors: rosato be. Am J Hematol. 2018 May;93(5):672-682. doi: 10.1002/ajh.25058. Epub 2018 Feb 24. Am J Hematol. 2018. PMID: 29396846 Free article.

4

Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients.

Andolfo I, Russo R, Rosato BE, Manna F, Gambale A, Brugnara C, Iolascon A. Andolfo I, et al. Among authors: rosato be. Am J Hematol. 2018 Dec;93(12):1509-1517. doi: 10.1002/ajh.25276. Epub 2018 Oct 2. Am J Hematol. 2018. PMID: 30187933 Free article.

5

PIEZO1 Hypomorphic Variants in Congenital Lymphatic Dysplasia Cause Shape and Hydration Alterations of Red Blood Cells.

Andolfo I, De Rosa G, Errichiello E, Manna F, Rosato BE, Gambale A, Vetro A, Calcaterra V, Pelizzo G, De Franceschi L, Zuffardi O, Russo R, Iolascon A. Andolfo I, et al. Among authors: rosato be. Front Physiol. 2019 Mar 15;10:258. doi: 10.3389/fphys.2019.00258. eCollection 2019. Front Physiol. 2019. PMID: 30930797 Free PMC article.

6

Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein.

Russo R, Marra R, Andolfo I, De Rosa G, Rosato BE, Manna F, Gambale A, Raia M, Unal S, Barella S, Iolascon A. Russo R, et al. Among authors: rosato be. Front Physiol. 2019 May 22;10:621. doi: 10.3389/fphys.2019.00621. eCollection 2019. Front Physiol. 2019. PMID: 31191338 Free PMC article.

7

The BMP-SMAD pathway mediates the impaired hepatic iron metabolism associated with the ERFE-A260S variant.

Andolfo I, Rosato BE, Marra R, De Rosa G, Manna F, Gambale A, Iolascon A, Russo R. Andolfo I, et al. Among authors: rosato be. Am J Hematol. 2019 Nov;94(11):1227-1235. doi: 10.1002/ajh.25613. Epub 2019 Aug 30. Am J Hematol. 2019. PMID: 31400017 Free article.

8

Gain-of-function mutations in PIEZO1 directly impair hepatic iron metabolism via the inhibition of the BMP/SMADs pathway.

Andolfo I, Rosato BE, Manna F, De Rosa G, Marra R, Gambale A, Girelli D, Russo R, Iolascon A. Andolfo I, et al. Among authors: rosato be. Am J Hematol. 2020 Feb;95(2):188-197. doi: 10.1002/ajh.25683. Epub 2019 Dec 9. Am J Hematol. 2020. PMID: 31737919 Free article.

9

Kinome multigenic panel identified novel druggable EPHB4-V871I somatic variant in high-risk neuroblastoma.

Andolfo I, Lasorsa VA, Manna F, Rosato BE, Formicola D, Iolascon A, Capasso M. Andolfo I, et al. Among authors: rosato be. J Cell Mol Med. 2020 Jun;24(11):6459-6471. doi: 10.1111/jcmm.15297. Epub 2020 Apr 26. J Cell Mol Med. 2020. PMID: 32336043 Free PMC article.

10

RAP-011 Rescues the Disease Phenotype in a Cellular Model of Congenital Dyserythropoietic Anemia Type II by Inhibiting the SMAD2-3 Pathway.

De Rosa G, Andolfo I, Marra R, Manna F, Rosato BE, Iolascon A, Russo R. De Rosa G, et al. Among authors: rosato be. Int J Mol Sci. 2020 Aug 4;21(15):5577. doi: 10.3390/ijms21155577. Int J Mol Sci. 2020. PMID: 32759740 Free PMC article.

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