Celato A - Search Results

1

A new form of cerebral folate deficiency with severe self-injurious behaviour.

Leuzzi V, Mastrangelo M, Celato A, Carducci C, Carducci C. Leuzzi V, et al. Among authors: celato a. Acta Paediatr. 2012 Nov;101(11):e482-3. doi: 10.1111/j.1651-2227.2012.02800.x. Epub 2012 Sep 13. Acta Paediatr. 2012. PMID: 22861007 No abstract available.

2

A diagnostic algorithm for the evaluation of early onset genetic-metabolic epileptic encephalopathies.

Mastrangelo M, Celato A, Leuzzi V. Mastrangelo M, et al. Among authors: celato a. Eur J Paediatr Neurol. 2012 Mar;16(2):179-91. doi: 10.1016/j.ejpn.2011.07.015. Epub 2011 Sep 21. Eur J Paediatr Neurol. 2012. PMID: 21940184 Review.

3

Diagnostic work-up and therapeutic options in management of pediatric status epilepticus.

Mastrangelo M, Celato A. Mastrangelo M, et al. Among authors: celato a. World J Pediatr. 2012 May;8(2):109-15. doi: 10.1007/s12519-012-0348-2. Epub 2012 May 10. World J Pediatr. 2012. PMID: 22573420 Review.

4

A new case of malonic aciduria with a presymptomatic diagnosis and an early treatment.

Celato A, Mitola C, Tolve M, Giannini MT, De Leo S, Carducci C, Carducci C, Leuzzi V. Celato A, et al. Brain Dev. 2013 Aug;35(7):675-80. doi: 10.1016/j.braindev.2012.10.014. Epub 2012 Nov 22. Brain Dev. 2013. PMID: 23177061

5

The long-term treatment of a patient with type 1 diabetes mellitus and glutaric aciduria type 1: the effect of insulin.

Del Rizzo M, Galderisi A, Celato A, Furlan F, Giordano L, Cazzorla C, Fasan I, Moretti C, Zschocke J, Burlina AB. Del Rizzo M, et al. Among authors: celato a. Eur J Pediatr. 2016 Aug;175(8):1123-8. doi: 10.1007/s00431-016-2699-5. Epub 2016 Feb 5. Eur J Pediatr. 2016. PMID: 26847429

6

Current insights into familial spastic paraparesis: new advances in an old disease.

Fortini D, Cricchi F, Di Fabio R, Damiano M, Comanducci G, Benedetti L, Valoppi M, Grieco GS, D'Eugenio O, Celato A, Santorelli F, Casali C, Amabile GA, Pierelli F. Fortini D, et al. Among authors: celato a. Funct Neurol. 2003 Jan-Mar;18(1):43-9. Funct Neurol. 2003. PMID: 12760414 Review.

7

The neurological and psychological phenotype of adult patients with early-treated phenylketonuria: A systematic review.

Burlina AP, Lachmann RH, Manara R, Cazzorla C, Celato A, van Spronsen FJ, Burlina A. Burlina AP, et al. Among authors: celato a. J Inherit Metab Dis. 2019 Mar;42(2):209-219. doi: 10.1002/jimd.12065. J Inherit Metab Dis. 2019. PMID: 30690773

8

Clinical, biochemical and molecular characterization of prosaposin deficiency.

Motta M, Tatti M, Furlan F, Celato A, Di Fruscio G, Polo G, Manara R, Nigro V, Tartaglia M, Burlina A, Salvioli R. Motta M, et al. Among authors: celato a. Clin Genet. 2016 Sep;90(3):220-9. doi: 10.1111/cge.12753. Epub 2016 Feb 19. Clin Genet. 2016. PMID: 26831127

9

Quality of Life (QoL) assessment in a cohort of patients with phenylketonuria.

Cazzorla C, Cegolon L, Burlina AP, Celato A, Massa P, Giordano L, Polo G, Daniele A, Salvatore F, Burlina AB. Cazzorla C, et al. Among authors: celato a. BMC Public Health. 2014 Dec 4;14:1243. doi: 10.1186/1471-2458-14-1243. BMC Public Health. 2014. PMID: 25471331 Free PMC article.

10

The Utility of CSF for the Diagnosis of Primary and Secondary Monoamine Neurotransmitter Deficiencies.

Burlina AB, Celato A, Polo G, Edini C, Burlina AP. Burlina AB, et al. Among authors: celato a. EJIFCC. 2017 Mar 8;28(1):64-76. eCollection 2017 Mar. EJIFCC. 2017. PMID: 28439219 Free PMC article.

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