Moricca MT - Search Results

1

Long-term treatment of phenylketonuria with a new medical food containing large neutral amino acids.

Concolino D, Mascaro I, Moricca MT, Bonapace G, Matalon K, Trapasso J, Radhakrishnan G, Ferrara C, Matalon R, Strisciuglio P. Concolino D, et al. Among authors: moricca mt. Eur J Clin Nutr. 2017 Jan;71(1):51-55. doi: 10.1038/ejcn.2016.166. Epub 2016 Sep 14. Eur J Clin Nutr. 2017. PMID: 27623981 Free PMC article.

2

Normal serum levels of vitamin B12 and folic acid in children with phenylketonuria.

Strisciuglio P, Concolino D, Moricca MT, Rivalta L, Parlato G. Strisciuglio P, et al. Among authors: moricca mt. Eur J Pediatr. 1995 Oct;154(10):866. doi: 10.1007/BF01959802. Eur J Pediatr. 1995. PMID: 8529692 No abstract available.

3

Partial trisomy 1(q42-->qter): a new case with a mild phenotype.

Concolino D, Cinti R, Ferraro L, Moricca MT, Strisciuglio P. Concolino D, et al. Among authors: moricca mt. J Med Genet. 1998 Jan;35(1):75-7. doi: 10.1136/jmg.35.1.75. J Med Genet. 1998. PMID: 9475102 Free PMC article. Review.

4

Centric fission of chromosome 9 in a boy with trisomy 9p.

Concolino D, Cinti R, Moricca M, Andria G, Strisciuglio P. Concolino D, et al. Am J Med Genet. 1998 Aug 27;79(1):35-7. doi: 10.1002/(sici)1096-8628(19980827)79:1<35::aid-ajmg9>3.0.co;2-h. Am J Med Genet. 1998. PMID: 9738866

5

Serum prolactin as a tool for the follow-up of treated DHPR-deficient patients.

Concolino D, Muzzi G, Rapsomaniki M, Moricca MT, Pascale MG, Strisciuglio P. Concolino D, et al. Among authors: moricca mt. J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S193-7. doi: 10.1007/s10545-007-0788-3. Epub 2008 Apr 15. J Inherit Metab Dis. 2008. PMID: 18425437

6

Co-existence of phenylketonuria and Fabry disease on a 3 year-old boy: case report.

Concolino D, Rapsomaniki M, Disabella E, Sestito S, Pascale MG, Moricca MT, Bonapace G, Arbustini E, Strisciuglio P. Concolino D, et al. Among authors: moricca mt. BMC Pediatr. 2010 May 17;10:32. doi: 10.1186/1471-2431-10-32. BMC Pediatr. 2010. PMID: 20478016 Free PMC article.

7

A de novo 8q22.2-24.3 duplication in a patient with mild phenotype.

Concolino D, Iembo MA, Moricca MT, Rapsomaniki M, Marotta R, Galesi O, Fichera M, Romano C, Strisciuglio P. Concolino D, et al. Among authors: moricca mt. Eur J Med Genet. 2012 Jan;55(1):67-70. doi: 10.1016/j.ejmg.2011.09.001. Epub 2011 Sep 25. Eur J Med Genet. 2012. PMID: 21971480

8

Identification of two novel mutations on CLCN7 gene in a patient with malignant ostopetrosis.

Bonapace G, Moricca MT, Talarico V, Graziano F, Pensabene L, Miniero R. Bonapace G, et al. Among authors: moricca mt. Ital J Pediatr. 2014 Nov 20;40:90. doi: 10.1186/s13052-014-0090-6. Ital J Pediatr. 2014. PMID: 25410126 Free PMC article.

9

Norrbottnian clinical variant of Gaucher disease in Southern Italy.

Sestito S, Filocamo M, Ceravolo F, Falvo F, Grisolia M, Moricca MT, Cantaffa R, Grossi S, Strisciuglio P, Concolino D. Sestito S, et al. Among authors: moricca mt. J Hum Genet. 2017 Apr;62(4):507-511. doi: 10.1038/jhg.2016.158. Epub 2016 Dec 22. J Hum Genet. 2017. PMID: 28003644

10

Combination therapy in a patient with chronic neuronopathic Gaucher disease: a case report.

Ceravolo F, Grisolia M, Sestito S, Falvo F, Moricca MT, Concolino D. Ceravolo F, et al. Among authors: moricca mt. J Med Case Rep. 2017 Jan 20;11(1):19. doi: 10.1186/s13256-016-1147-5. J Med Case Rep. 2017. PMID: 28103924 Free PMC article.

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