Ruggieri M - Search Results

1

Highlights on Genomics Applications for Lysosomal Storage Diseases.

La Cognata V, Guarnaccia M, Polizzi A, Ruggieri M, Cavallaro S. La Cognata V, et al. Among authors: ruggieri m. Cells. 2020 Aug 14;9(8):1902. doi: 10.3390/cells9081902. Cells. 2020. PMID: 32824006 Free PMC article. Review.

2

Hypertrichosis cubiti (hairy elbow syndrome): a clue to a malformation syndrome.

Polizzi A, Pavone P, Ciancio E, La Rosa C, Sorge G, Ruggieri M. Polizzi A, et al. Among authors: ruggieri m. J Pediatr Endocrinol Metab. 2005 Oct;18(10):1019-25. doi: 10.1515/jpem.2005.18.10.1019. J Pediatr Endocrinol Metab. 2005. PMID: 16355816 Review.

3

Septo-optic dysplasia complex: a heterogeneous malformation syndrome.

Polizzi A, Pavone P, Iannetti P, Manfré L, Ruggieri M. Polizzi A, et al. Among authors: ruggieri m. Pediatr Neurol. 2006 Jan;34(1):66-71. doi: 10.1016/j.pediatrneurol.2005.07.004. Pediatr Neurol. 2006. PMID: 16376284

4

Bilateral periventricular nodular heterotopia with amniotic band syndrome.

Ruggieri M, Spalice A, Polizzi A, Roggini M, Iannetti P. Ruggieri M, et al. Pediatr Neurol. 2007 Jun;36(6):407-10. doi: 10.1016/j.pediatrneurol.2007.02.006. Pediatr Neurol. 2007. PMID: 17560504

5

Low prevalence of neurologic and psychiatric manifestations in children with gluten sensitivity.

Ruggieri M, Incorpora G, Polizzi A, Parano E, Spina M, Pavone P. Ruggieri M, et al. J Pediatr. 2008 Feb;152(2):244-9. doi: 10.1016/j.jpeds.2007.06.042. Epub 2007 Nov 19. J Pediatr. 2008. PMID: 18206697

6

Neurofibromatosis type 1 and infantile spasms.

Ruggieri M, Iannetti P, Clementi M, Polizzi A, Incorpora G, Spalice A, Pavone P, Praticò AD, Elia M, Gabriele AL, Tenconi R, Pavone L. Ruggieri M, et al. Childs Nerv Syst. 2009 Feb;25(2):211-6. doi: 10.1007/s00381-008-0706-5. Epub 2008 Sep 19. Childs Nerv Syst. 2009. PMID: 18802710

7

Infantile spasms in the setting of Sturge-Weber syndrome.

Barbagallo M, Ruggieri M, Incorpora G, Pavone P, Nucifora C, Spalice A, Praticò AD, Polizzi A, Pavone L, Iannetti P. Barbagallo M, et al. Among authors: ruggieri m. Childs Nerv Syst. 2009 Jan;25(1):111-8. doi: 10.1007/s00381-008-0705-6. Epub 2008 Oct 2. Childs Nerv Syst. 2009. PMID: 18830609

8

Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke.

Barbagallo M, Pavone P, Incorpora G, Domenico Praticò A, Romantshik O, Friso S, Spalice A, Nicita F, Polizzi A, Ruggieri M, Iannetti P. Barbagallo M, et al. Among authors: ruggieri m. Childs Nerv Syst. 2009 Mar;25(3):361-5. doi: 10.1007/s00381-008-0724-3. Epub 2008 Oct 29. Childs Nerv Syst. 2009. PMID: 18958479

9

Dysembryoplastic neuroepithelial tumors: a prospective clinicopathologic and outcome study of 13 children.

Spalice A, Ruggieri M, Grosso S, Verrotti A, Polizzi A, Magro G, Caltabiano R, Pavone P, Del Balzo F, Platania N, Iannetti P. Spalice A, et al. Among authors: ruggieri m. Pediatr Neurol. 2010 Dec;43(6):395-402. doi: 10.1016/j.pediatrneurol.2010.06.017. Pediatr Neurol. 2010. PMID: 21093729

10

Spectrum of skeletal abnormalities in a complex malformation syndrome with "cutis tricolor" (Ruggieri-Happle syndrome).

Ruggieri M, Roggini M, Kennerknecht I, Polizzi A, Distefano A, Pavone V. Ruggieri M, et al. Acta Paediatr. 2011 Jan;100(1):121-7. doi: 10.1111/j.1651-2227.2010.01970.x. Acta Paediatr. 2011. PMID: 21143296

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