Elena D’Amato - Search Results

Year	Number of Results
2005	3
2007	1
2008	3
2009	1
2010	1
2012	1
2014	1
2016	1
2017	1
2019	2
2024	0

1

Metabolic Bone Disease of Prematurity: Diagnosis and Management.

Faienza MF, D'Amato E, Natale MP, Grano M, Chiarito M, Brunetti G, D'Amato G. Faienza MF, et al. Among authors: d amato e. Front Pediatr. 2019 Apr 12;7:143. doi: 10.3389/fped.2019.00143. eCollection 2019. Front Pediatr. 2019. PMID: 31032241 Free PMC article. Review.

2

Sudden death in Unverricht-Lundborg patients: is serotonin the key?

Striano P, D'Amato E, Pezzella M, Mainardi P, Zara F, Striano S. Striano P, et al. Among authors: d amato e. Neurol Sci. 2010 Feb;31(1):115-6. doi: 10.1007/s10072-009-0193-9. Epub 2009 Dec 2. Neurol Sci. 2010. PMID: 19953285 No abstract available.

3

Toll-like receptor 4 signalling mediates inflammation in skeletal muscle of patients with chronic kidney disease.

Verzola D, Bonanni A, Sofia A, Montecucco F, D'Amato E, Cademartori V, Parodi EL, Viazzi F, Venturelli C, Brunori G, Garibotto G. Verzola D, et al. Among authors: d amato e. J Cachexia Sarcopenia Muscle. 2017 Feb;8(1):131-144. doi: 10.1002/jcsm.12129. Epub 2016 Oct 18. J Cachexia Sarcopenia Muscle. 2017. PMID: 27897392 Free PMC article.

4

Lysine triggers apoptosis through a NADPH oxidase-dependent mechanism in human renal tubular cells.

Verzola D, Famà A, Villaggio B, Di Rocco M, Simonato A, D'Amato E, Gianiorio F, Garibotto G. Verzola D, et al. Among authors: d amato e. J Inherit Metab Dis. 2012 Nov;35(6):1011-9. doi: 10.1007/s10545-012-9468-z. Epub 2012 Mar 9. J Inherit Metab Dis. 2012. PMID: 22403019

5

Wolfram syndrome (diabetes insipidus, diabetes, optic atrophy, and deafness): clinical and genetic study.

d'Annunzio G, Minuto N, D'Amato E, de Toni T, Lombardo F, Pasquali L, Lorini R. d'Annunzio G, et al. Among authors: d amato e. Diabetes Care. 2008 Sep;31(9):1743-5. doi: 10.2337/dc08-0178. Epub 2008 Jun 19. Diabetes Care. 2008. PMID: 18566338 Free PMC article.

6

Reduced serotonin and 3-hydroxyanthranilic acid levels in serum of cystatin B-deficient mice, a model system for progressive myoclonus epilepsy.

Arbatova J, D'Amato E, Vaarmann A, Zharkovsky A, Reeben M. Arbatova J, et al. Among authors: d amato e. Epilepsia. 2005;46 Suppl 5:49-51. doi: 10.1111/j.1528-1167.2005.01008.x. Epilepsia. 2005. PMID: 15987253 Free article.

7

Unusual ultrasonographic finding of ovarian hyperstimulation syndrome in a preterm newborn with severe intra-uterine growth retardation.

D'Amato G, D'Amato E, Natale MP, Brunetti G, Faienza MF. D'Amato G, et al. Among authors: d amato e. J Paediatr Child Health. 2019 Sep;55(9):1139-1141. doi: 10.1111/jpc.14439. Epub 2019 Mar 28. J Paediatr Child Health. 2019. PMID: 30924252 No abstract available.

8

KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes.

Massa O, Iafusco D, D'Amato E, Gloyn AL, Hattersley AT, Pasquino B, Tonini G, Dammacco F, Zanette G, Meschi F, Porzio O, Bottazzo G, Crinó A, Lorini R, Cerutti F, Vanelli M, Barbetti F; Early Onset Diabetes Study Group of the Italian Society of Pediatric Endocrinology and Diabetology. Massa O, et al. Among authors: d amato e. Hum Mutat. 2005 Jan;25(1):22-7. doi: 10.1002/humu.20124. Hum Mutat. 2005. PMID: 15580558

9

Horseshoe kidney malformation in Turner syndrome is not associated with HNF-1beta gene mutations.

D'Amato E, d'Annunzio G, Calcaterra V, Morsellino V, Larizza D, Lorini R. D'Amato E, et al. Pediatr Nephrol. 2008 Jan;23(1):137-40. doi: 10.1007/s00467-007-0609-9. Epub 2007 Oct 6. Pediatr Nephrol. 2008. PMID: 17922147

10

Enhanced glomerular Toll-like receptor 4 expression and signaling in patients with type 2 diabetic nephropathy and microalbuminuria.

Verzola D, Cappuccino L, D'Amato E, Villaggio B, Gianiorio F, Mij M, Simonato A, Viazzi F, Salvidio G, Garibotto G. Verzola D, et al. Among authors: d amato e. Kidney Int. 2014 Dec;86(6):1229-43. doi: 10.1038/ki.2014.116. Epub 2014 Apr 30. Kidney Int. 2014. PMID: 24786705 Free article.

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