Pavone P - Search Results

1

Microcephaly associated with Legg-Calvè-Perthes disease in two siblings.

Savasta S, Ruggieri M, Pavone P, Praticò AD, Polizzi A, Beluffi G, Pavone V. Savasta S, et al. Among authors: pavone p, pavone v. Neurol Sci. 2012 Dec;33(6):1401-5. doi: 10.1007/s10072-011-0891-y. Epub 2012 Jan 6. Neurol Sci. 2012. PMID: 22222936

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

Arthrogryposis multiplex congenita and pituitary ectopia. A case report.

Parano E, Trifiletti RR, Barone R, Pavone V, Pavone P. Parano E, et al. Among authors: pavone p, pavone v. Neuropediatrics. 2000 Dec;31(6):325-7. doi: 10.1055/s-2000-12957. Neuropediatrics. 2000. PMID: 11508555

5

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

6

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.

7

CNS findings in three cases of septo-optic dysplasia, including one with semilobar holoprosencephaly.

Polizzi A, Pavone P, Iannetti P, Gambardella A, Ruggieri M. Polizzi A, et al. Among authors: pavone p. Am J Med Genet A. 2005 Aug 1;136A(4):357. doi: 10.1002/ajmg.a.30630. Am J Med Genet A. 2005. PMID: 15942946 No abstract available.

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

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: pavone p. 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.

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