Pavone P - Search Results

1

Congenital familial myasthenic syndromes: disease and course in an affected dizygotic twin pair.

Pavone P, Praticò AD, Pavone V, Falsaperla R. Pavone P, et al. Among authors: pavone v. BMJ Case Rep. 2013 Jan 29;2013:bcr2012007651. doi: 10.1136/bcr-2012-007651. BMJ Case Rep. 2013. PMID: 23365176 Free PMC article.

2

Extraordinary intrathecal bone reaction in beta-thalassaemia intermedia.

Parano E, Pavone V, Di Gregorio F, Pavone P, Trifiletti RR. Parano E, et al. Among authors: pavone p, pavone v. Lancet. 1999 Sep 11;354(9182):922. doi: 10.1016/s0140-6736(99)03587-4. Lancet. 1999. PMID: 10489960 Free article.

3

[Post-influenza viral myositis: report of a case].

Pavone P, Trobia GL, Sciacca T, Parano E, Sciacca P, Falsaperla R. Pavone P, et al. Pediatr Med Chir. 1999 Mar-Apr;21(2):79-81. Pediatr Med Chir. 1999. PMID: 10570786 Italian.

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

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

6

Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: a novel form of CMD.

Voit T, Parano E, Straub V, Schröder JM, Schaper J, Pavone P, Falsaperla R, Pavone L, Herrmann R. Voit T, et al. Among authors: pavone l, pavone p. Neuromuscul Disord. 2002 Oct;12(7-8):623-30. doi: 10.1016/s0960-8966(02)00018-4. Neuromuscul Disord. 2002. PMID: 12207929

7

Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease.

Taniguchi K, Kobayashi K, Saito K, Yamanouchi H, Ohnuma A, Hayashi YK, Manya H, Jin DK, Lee M, Parano E, Falsaperla R, Pavone P, Van Coster R, Talim B, Steinbrecher A, Straub V, Nishino I, Topaloglu H, Voit T, Endo T, Toda T. Taniguchi K, et al. Among authors: pavone p. Hum Mol Genet. 2003 Mar 1;12(5):527-34. doi: 10.1093/hmg/ddg043. Hum Mol Genet. 2003. PMID: 12588800

8

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

9

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

10

Pseudohypoparathyroidism Ia with Evans syndrome.

Pavone P, Praticò AD, Castellano-Chiodo D, Ruggieri M. Pavone P, et al. J Pediatr Hematol Oncol. 2008 Aug;30(8):628-30. doi: 10.1097/MPH.0b013e318175890f. J Pediatr Hematol Oncol. 2008. PMID: 18799944

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