Parano E - Search Results

1

Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review.

Pavone P, Marino L, Cacciaguerra G, Di Nora A, Parano E, Musumeci G, Ruggieri M, Polizzi A, Falsaperla R. Pavone P, et al. Among authors: parano e. Children (Basel). 2023 Aug 21;10(8):1421. doi: 10.3390/children10081421. Children (Basel). 2023. PMID: 37628420 Free PMC article. Review.

2

Reversible palsy of the hypoglossal nerve complicating infectious mononucleosis in a young child.

Parano E, Giuffrida S, Restivo D, Saponara R, Greco F, Trifiletti RR. Parano E, et al. Neuropediatrics. 1998 Feb;29(1):46-7. doi: 10.1055/s-2007-973534. Neuropediatrics. 1998. PMID: 9553950

3

Reflex sympathetic dystrophy associated with deep peroneal nerve entrapment.

Parano E, Pavone V, Greco F, Majorana M, Trifiletti RR. Parano E, et al. Brain Dev. 1998 Mar;20(2):80-2. doi: 10.1016/s0387-7604(97)00106-x. Brain Dev. 1998. PMID: 9545176 Free article.

4

Electrophysiologic correlates of peripheral nervous system maturation in infancy and childhood.

Parano E, Uncini A, De Vivo DC, Lovelace RE. Parano E, et al. J Child Neurol. 1993 Oct;8(4):336-8. doi: 10.1177/088307389300800408. J Child Neurol. 1993. PMID: 8228028

5

Walker-Warburg syndrome.

Parano E. Parano E. Neuropediatrics. 1990 Nov;21(4):224. doi: 10.1055/s-2008-1071503. Neuropediatrics. 1990. PMID: 2290488 No abstract available.

6

A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions.

Carter TA, Bönnemann CG, Wang CH, Obici S, Parano E, De Fatima Bonaldo M, Ross BM, Penchaszadeh GK, Mackenzie A, Soares MB, Kunkel LM, Gilliam TC. Carter TA, et al. Among authors: parano e. Hum Mol Genet. 1997 Feb;6(2):229-36. doi: 10.1093/hmg/6.2.229. Hum Mol Genet. 1997. PMID: 9063743

7

[Heart involvement in progressive spinal muscular atrophy. A review of the literature and case histories in childhood].

Distefano G, Sciacca P, Parisi MG, Parano E, Smilari P, Marletta M, Fiumara A. Distefano G, et al. Among authors: parano e. Pediatr Med Chir. 1994 Mar-Apr;16(2):125-8. Pediatr Med Chir. 1994. PMID: 8078785 Review. Italian.

8

Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses.

Shah AB, Chernov I, Zhang HT, Ross BM, Das K, Lutsenko S, Parano E, Pavone L, Evgrafov O, Ivanova-Smolenskaya IA, Annerén G, Westermark K, Urrutia FH, Penchaszadeh GK, Sternlieb I, Scheinberg IH, Gilliam TC, Petrukhin K. Shah AB, et al. Among authors: parano e. Am J Hum Genet. 1997 Aug;61(2):317-28. doi: 10.1086/514864. Am J Hum Genet. 1997. PMID: 9311736 Free PMC article.

9

TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa.

Banerjee P, Kleyn PW, Knowles JA, Lewis CA, Ross BM, Parano E, Kovats SG, Lee JJ, Penchaszadeh GK, Ott J, Jacobson SG, Gilliam TC. Banerjee P, et al. Among authors: parano e. Nat Genet. 1998 Feb;18(2):177-9. doi: 10.1038/ng0298-177. Nat Genet. 1998. PMID: 9462751

10

[Surgical therapy in gastroesophageal reflux disease].

Ingegneros L, Pepe G, Pepe F, Monciino P, Rizza G, Parano E, Basile F, Calì V. Ingegneros L, et al. Among authors: parano e. Minerva Chir. 1987 Jun 30;42(12):1023-6. Minerva Chir. 1987. PMID: 3627512 Italian. No abstract available.

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