Pavone P - Search Results

1

Pavone P, Polizzi A, Marino SD, Corsello G, Falsaperla R, Marino S, Ruggieri M. Pavone P, et al. Neurol Sci. 2020 Dec;41(12):3547-3562. doi: 10.1007/s10072-020-04600-5. Epub 2020 Aug 22. Neurol Sci. 2020. PMID: 32827285 Free PMC article. Review.

2

Colobomatous microphthalmia, microcephaly with cerebellar hypoplasia: association or new syndrome?

Pavone P, Parano E, Polizzi A, Trifiletti RR. Pavone P, et al. Am J Med Genet. 2000 Jun 5;92(4):278-80. Am J Med Genet. 2000. PMID: 10842296

3

Lack of progression of brain atrophy in Aicardi-Goutières syndrome.

Polizzi A, Pavone P, Parano E, Incorpora G, Ruggieri M. Polizzi A, et al. Among authors: pavone p. Pediatr Neurol. 2001 Apr;24(4):300-2. doi: 10.1016/s0887-8994(00)00268-x. Pediatr Neurol. 2001. PMID: 11377106

4

Long-term survival in a child with arthrogryposis multiplex congenita and spinal muscular atrophy.

Falsaperla R, Romeo G, Di Giorgio A, Pavone P, Parano E, Connolly AM. Falsaperla R, et al. Among authors: pavone p. J Child Neurol. 2001 Dec;16(12):934-6. doi: 10.1177/088307380101601213. J Child Neurol. 2001. PMID: 11785510

5

Peripheral neuropathy as first sign of ulcerative colitis in a child.

Greco F, Pavone P, Falsaperla R, Sorge G. Greco F, et al. Among authors: pavone p. J Clin Gastroenterol. 2004 Feb;38(2):115-7. doi: 10.1097/00004836-200402000-00006. J Clin Gastroenterol. 2004. PMID: 14745284

6

Epilepsy is not a prominent feature of primary autism.

Pavone P, Incorpora G, Fiumara A, Parano E, Trifiletti RR, Ruggieri M. Pavone P, et al. Neuropediatrics. 2004 Aug;35(4):207-10. doi: 10.1055/s-2004-821079. Neuropediatrics. 2004. PMID: 15328558

7

Ophthalmological manifestations in segmental neurofibromatosis type 1.

Ruggieri M, Pavone P, Polizzi A, Di Pietro M, Scuderi A, Gabriele A, Spalice A, Iannetti P. Ruggieri M, et al. Among authors: pavone p. Br J Ophthalmol. 2004 Nov;88(11):1429-33. doi: 10.1136/bjo.2004.043802. Br J Ophthalmol. 2004. PMID: 15489488 Free PMC article.

8

A complex brain malformation syndrome with rhombencephalosynapsis, preaxial hexadactyly plus facial and skull anomalies.

Pavone P, Incorpora G, Ruggieri M. Pavone P, et al. Neuropediatrics. 2005 Aug;36(4):279-83. doi: 10.1055/s-2005-872813. Neuropediatrics. 2005. PMID: 16138255

9

Callosal anomalies with interhemispheric cyst: expanding the phenotype.

Pavone P, Barone R, Baieli S, Parano E, Incorpora G, Ruggieri M. Pavone P, et al. Acta Paediatr. 2005 Aug;94(8):1066-72. doi: 10.1111/j.1651-2227.2005.tb02047.x. Acta Paediatr. 2005. PMID: 16188851

10

Subclinical cardiological involvement in Sicilian patients with pure congenital muscular dystrophy.

Falsaperla R, Romeo G, Mattia C, Pavone P, Quattrocchi S. Falsaperla R, et al. Among authors: pavone p. Minerva Pediatr. 2005 Oct;57(5):275-9. Minerva Pediatr. 2005. PMID: 16205611

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