Laverda AM - Search Results

1

Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: a CoQ10-responsive condition.

Salviati L, Sacconi S, Murer L, Zacchello G, Franceschini L, Laverda AM, Basso G, Quinzii C, Angelini C, Hirano M, Naini AB, Navas P, DiMauro S, Montini G. Salviati L, et al. Among authors: laverda am. Neurology. 2005 Aug 23;65(4):606-8. doi: 10.1212/01.wnl.0000172859.55579.a7. Neurology. 2005. PMID: 16116126

2

Diffusion-weighted imaging findings in hemolytic uremic syndrome with central nervous system involvement.

Toldo I, Manara R, Cogo P, Sartori S, Murer L, Battistella PA, Laverda AM. Toldo I, et al. Among authors: laverda am. J Child Neurol. 2009 Feb;24(2):247-50. doi: 10.1177/0883073808323022. Epub 2008 Dec 12. J Child Neurol. 2009. PMID: 19074752

3

Acute quadriplegic myopathy in a 17-month-old boy.

Salviati L, Laverda AM, Zancan L, Fanin M, Angelini C, Meznaric-Petrusa M. Salviati L, et al. Among authors: laverda am. J Child Neurol. 2000 Jan;15(1):63-6. doi: 10.1177/088307380001500115. J Child Neurol. 2000. PMID: 10641615

4

Diencephalic syndrome and disseminated juvenile pilocytic astrocytomas of the hypothalamic-optic chiasm region.

Perilongo G, Carollo C, Salviati L, Murgia A, Pillon M, Basso G, Gardiman M, Laverda A. Perilongo G, et al. Cancer. 1997 Jul 1;80(1):142-6. doi: 10.1002/(sici)1097-0142(19970701)80:1<142::aid-cncr19>3.0.co;2-y. Cancer. 1997. PMID: 9210720

5

Increased level of N-acetylaspartylglutamate (NAAG) in the CSF of a patient with Pelizaeus-Merzbacher-like disease due to mutation in the GJA12 gene.

Sartori S, Burlina AB, Salviati L, Trevisson E, Toldo I, Laverda AM, Burlina AP. Sartori S, et al. Among authors: laverda am. Eur J Paediatr Neurol. 2008 Jul;12(4):348-50. doi: 10.1016/j.ejpn.2007.07.011. Epub 2007 Sep 18. Eur J Paediatr Neurol. 2008. PMID: 17881259

6

Dandy-Walker malformation masking the molar tooth sign: an illustrative case with magnetic resonance imaging follow-up.

Sartori S, Ludwig K, Fortuna M, Marzocchi C, Calderone M, Toldo I, Salviati L, Laverda AM, Tenconi R. Sartori S, et al. Among authors: laverda am. J Child Neurol. 2010 Nov;25(11):1419-22. doi: 10.1177/0883073810370477. Epub 2010 Sep 7. J Child Neurol. 2010. PMID: 20823032

7

A novel deletion in the GJA12 gene causes Pelizaeus-Merzbacher-like disease.

Salviati L, Trevisson E, Baldoin MC, Toldo I, Sartori S, Calderone M, Tenconi R, Laverda A. Salviati L, et al. Neurogenetics. 2007 Jan;8(1):57-60. doi: 10.1007/s10048-006-0065-x. Epub 2006 Oct 10. Neurogenetics. 2007. PMID: 17031678

8

Neurogenic vesico-urethral dysfunction in children with cerebral palsy.

Drigo P, Seren F, Artibani W, Laverda AM, Battistella PA, Zacchello G. Drigo P, et al. Among authors: laverda am. Ital J Neurol Sci. 1988 Apr;9(2):151-4. doi: 10.1007/BF02337462. Ital J Neurol Sci. 1988. PMID: 3397269

9

Pre- and postprandial electroencephalography in glucose transporter type 1 deficiency syndrome: an illustrative case to discuss the concept of carbohydrate responsiveness.

Parolin G, Drigo P, Toldo I, Boniver C, Gatta M, Burlina A, Laverda AM, Sartori S. Parolin G, et al. Among authors: laverda am. J Child Neurol. 2011 Jan;26(1):103-8. doi: 10.1177/0883073810376444. J Child Neurol. 2011. PMID: 21212456

10

Fumarase deficiency is an autosomal recessive encephalopathy affecting both the mitochondrial and the cytosolic enzymes.

Gellera C, Uziel G, Rimoldi M, Zeviani M, Laverda A, Carrara F, DiDonato S. Gellera C, et al. Neurology. 1990 Mar;40(3 Pt 1):495-9. doi: 10.1212/wnl.40.3_part_1.495. Neurology. 1990. PMID: 2314594

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