Prato G - Search Results

1

Schimke immuno-osseous dysplasia, two new cases with peculiar EEG pattern.

Prato G, De Grandis E, Mancardi MM, Cordani R, Giacomini T, Pisciotta L, Uccella S, Severino M, Tortora D, Pavanello M, Bertamino M, Verrina E, Caridi G, Di Rocco M, Nobili L. Prato G, et al. Brain Dev. 2020 May;42(5):408-413. doi: 10.1016/j.braindev.2020.01.008. Epub 2020 Feb 27. Brain Dev. 2020. PMID: 32115305

2

Congenital segmental lymphedema in tuberous sclerosis complex with associated subependymal giant cell astrocytomas treated with Mammalian target of rapamycin inhibitors.

Prato G, Mancardi MM, Baglietto MG, Janis S, Vercellino N, Rossi A, Consales A, Raso A, Garrè ML. Prato G, et al. J Child Neurol. 2014 Sep;29(9):NP54-7. doi: 10.1177/0883073813499969. Epub 2013 Sep 20. J Child Neurol. 2014. PMID: 24056156

3

Epileptic encephalopathy with continuous spike and wave during sleep associated to periventricular leukomalacia.

De Grandis E, Mancardi MM, Carelli V, Carpaneto M, Morana G, Prato G, Mirabelli-Badenier M, Pinto F, Veneselli E, Baglietto MG. De Grandis E, et al. Among authors: prato g. J Child Neurol. 2014 Nov;29(11):1479-85. doi: 10.1177/0883073813508223. Epub 2013 Nov 28. J Child Neurol. 2014. PMID: 24293309

4

RORB gene and 9q21.13 microdeletion: report on a patient with epilepsy and mild intellectual disability.

Baglietto MG, Caridi G, Gimelli G, Mancardi M, Prato G, Ronchetto P, Cuoco C, Tassano E. Baglietto MG, et al. Among authors: prato g. Eur J Med Genet. 2014 Jan;57(1):44-6. doi: 10.1016/j.ejmg.2013.12.001. Epub 2013 Dec 17. Eur J Med Genet. 2014. PMID: 24355400

5

Early-Onset Shapiro Syndrome Variant Treated with Pizotifen: A Case Report.

Denegri L, Prato G, Mancardi MM, Schiaffino C, Striano P, Baglietto MG. Denegri L, et al. Among authors: prato g. Neurodiagn J. 2017;57(2):139-146. doi: 10.1080/21646821.2017.1309941. Neurodiagn J. 2017. PMID: 28622125

6

ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases.

Stagnaro M, Pisciotta L, Gherzi M, Di Rocco M, Gurrieri F, Parrini E, Prato G, Veneselli E, De Grandis E. Stagnaro M, et al. Among authors: prato g. Eur J Paediatr Neurol. 2018 Mar;22(2):264-271. doi: 10.1016/j.ejpn.2018.01.010. Epub 2018 Jan 31. Eur J Paediatr Neurol. 2018. PMID: 29396171

7

Epileptic Encephalopathy in Adams-Oliver Syndrome Associated to a New DOCK6 Mutation: A Peculiar Behavioral Phenotype.

Pisciotta L, Capra V, Accogli A, Giacomini T, Prato G, Tavares P, Pinto-Basto J, Morana G, Mancardi MM. Pisciotta L, et al. Among authors: prato g. Neuropediatrics. 2018 Jun;49(3):217-221. doi: 10.1055/s-0038-1639372. Epub 2018 Apr 9. Neuropediatrics. 2018. PMID: 29631299

8

ABCC6 mutations and early onset stroke: Two cases of a typical Pseudoxanthoma Elasticum.

Bertamino M, Severino M, Grossi A, Rusmini M, Tortora D, Gandolfo C, Pederzoli S, Malattia C, Picco P, Striano P, Ceccherini I, Di Rocco M; Gaslini Pediatric Stroke Group. Bertamino M, et al. Eur J Paediatr Neurol. 2018 Jul;22(4):725-728. doi: 10.1016/j.ejpn.2018.04.002. Epub 2018 Apr 12. Eur J Paediatr Neurol. 2018. PMID: 29709427

9

Reversible cerebral vasoconstriction complicating cerebral atherosclerotic vascular disease in Schimke immuno-osseous dysplasia.

Severino M, Giacomini T, Verrina E, Prato G, Rossi A. Severino M, et al. Among authors: prato g. Neuroradiology. 2018 Sep;60(9):885-888. doi: 10.1007/s00234-018-2052-y. Epub 2018 Jul 6. Neuroradiology. 2018. PMID: 29978300 No abstract available.

10

CNNM2 homozygous mutations cause severe refractory hypomagnesemia, epileptic encephalopathy and brain malformations.

Accogli A, Scala M, Calcagno A, Napoli F, Di Iorgi N, Arrigo S, Mancardi MM, Prato G, Pisciotta L, Nagel M, Severino M, Capra V. Accogli A, et al. Among authors: prato g. Eur J Med Genet. 2019 Mar;62(3):198-203. doi: 10.1016/j.ejmg.2018.07.014. Epub 2018 Jul 17. Eur J Med Genet. 2019. PMID: 30026055

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