Pessagno A - Search Results

1

MR imaging findings in 2 cases of late infantile GM1 gangliosidosis.

De Grandis E, Di Rocco M, Pessagno A, Veneselli E, Rossi A. De Grandis E, et al. Among authors: pessagno a. AJNR Am J Neuroradiol. 2009 Aug;30(7):1325-7. doi: 10.3174/ajnr.A1508. Epub 2009 Mar 11. AJNR Am J Neuroradiol. 2009. PMID: 19279282 Free PMC article.

2

Leigh Syndrome with COX deficiency and SURF1 gene mutations: MR imaging findings.

Rossi A, Biancheri R, Bruno C, Di Rocco M, Calvi A, Pessagno A, Tortori-Donati P. Rossi A, et al. Among authors: pessagno a. AJNR Am J Neuroradiol. 2003 Jun-Jul;24(6):1188-91. AJNR Am J Neuroradiol. 2003. PMID: 12812953 Free PMC article.

3

Presence of delayed myelination and macrocephaly in the sister of a patient with vacuolating leukoencephalopathy with subcortical cysts.

Biancheri R, Pisaturo C, Perrone MV, Pessagno A, Rossi A, Veneselli E. Biancheri R, et al. Among authors: pessagno a. Neuropediatrics. 2000 Dec;31(6):321-4. doi: 10.1055/s-2000-12949. Neuropediatrics. 2000. PMID: 11508554

4

Different molecular mechanisms leading to white matter hypomyelination in infantile onset lysosomal disorders.

Di Rocco M, Rossi A, Parenti G, Allegri AE, Filocamo M, Pessagno A, Tortori-Donati P, Minetti C, Biancheri R. Di Rocco M, et al. Among authors: pessagno a. Neuropediatrics. 2005 Aug;36(4):265-9. doi: 10.1055/s-2005-865863. Neuropediatrics. 2005. PMID: 16138252

5

Long-term follow-up of neuroblastoma-associated opsoclonus-myoclonus-ataxia syndrome.

De Grandis E, Parodi S, Conte M, Angelini P, Battaglia F, Gandolfo C, Pessagno A, Pistoia V, Mitchell WG, Pike M, Haupt R, Veneselli E. De Grandis E, et al. Among authors: pessagno a. Neuropediatrics. 2009 Jun;40(3):103-11. doi: 10.1055/s-0029-1237723. Epub 2009 Dec 17. Neuropediatrics. 2009. PMID: 20020394

6

Enhancing cranial nerves and cauda equina: an emerging magnetic resonance imaging pattern in metachromatic leukodystrophy and krabbe disease.

Morana G, Biancheri R, Dirocco M, Filocamo M, Marazzi MG, Pessagno A, Rossi A. Morana G, et al. Among authors: pessagno a. Neuropediatrics. 2009 Dec;40(6):291-4. doi: 10.1055/s-0030-1249654. Epub 2010 May 5. Neuropediatrics. 2009. PMID: 20446225

7

Anti-N-methyl-D-aspartate-receptor encephalitis in a four-year-old girl.

Biancheri R, Pessagno A, Baglietto MG, Irani SR, Rossi A, Giribaldi G, Badenier MM, Vincent A, Veneselli E. Biancheri R, et al. Among authors: pessagno a. J Pediatr. 2010 Feb;156(2):332-4. doi: 10.1016/j.jpeds.2009.07.057. J Pediatr. 2010. PMID: 20105645

8

Clinical and electroencephalographic features in patients with CDKL5 mutations: two new Italian cases and review of the literature.

Pintaudi M, Baglietto MG, Gaggero R, Parodi E, Pessagno A, Marchi M, Russo S, Veneselli E. Pintaudi M, et al. Among authors: pessagno a. Epilepsy Behav. 2008 Feb;12(2):326-31. doi: 10.1016/j.yebeh.2007.10.010. Epub 2007 Dec 11. Epilepsy Behav. 2008. PMID: 18063413 Review.

9

Aicardi-Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy.

Orcesi S, Pessagno A, Biancheri R, La Piana R, Mascaretti M, Rossi A, Rice GI, Crow YJ, Fazzi E, Veneselli E. Orcesi S, et al. Among authors: pessagno a. Eur J Paediatr Neurol. 2008 Sep;12(5):408-11. doi: 10.1016/j.ejpn.2007.10.005. Epub 2008 Feb 20. Eur J Paediatr Neurol. 2008. PMID: 18069026

10

GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease.

Caroli F, Biancheri R, Seri M, Rossi A, Pessagno A, Bugiani M, Corsolini F, Savasta S, Romano S, Antonelli C, Romano A, Pareyson D, Gambero P, Uziel G, Ravazzolo R, Ceccherini I, Filocamo M. Caroli F, et al. Among authors: pessagno a. Clin Genet. 2007 Nov;72(5):427-33. doi: 10.1111/j.1399-0004.2007.00869.x. Epub 2007 Sep 25. Clin Genet. 2007. PMID: 17894839

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