Pepe E - Search Results

1

Bilateral macrostomia associated with aqueductal stenosis and glial heterotopias.

Pepe E, Petricig P, Peretta P, Cinalli G. Pepe E, et al. Cleft Palate Craniofac J. 2007 Sep;44(5):558-61. doi: 10.1597/06-096.1. Cleft Palate Craniofac J. 2007. PMID: 17760484

2

[First choice treatment of the pediatric wrist ganglia].

Petricig P, Pepe E. Petricig P, et al. Among authors: pepe e. Minerva Pediatr. 2006 Aug;58(4):379-83. Minerva Pediatr. 2006. PMID: 17008847 Italian.

3

Oral, facial, digital, vertebral anomalies with psychomotor delay: a mild form of OFD type Gabrielli?

Ferrero GB, Valenzise M, Franco B, Defilippi C, Gregato G, Corsello G, Pepe E, Silengo M. Ferrero GB, et al. Among authors: pepe e. Am J Med Genet. 2002 Dec 1;113(3):291-4. doi: 10.1002/ajmg.10815. Am J Med Genet. 2002. PMID: 12439899

4

Nickel Gluconate-Mercurius Heel-Potentised Swine Organ Preparations: a new therapeutical approach for the primary treatment of pediatric ranula and intraoral mucocele.

Garofalo S, Briganti V, Cavallaro S, Pepe E, Prete M, Suteu L, Tavormina P. Garofalo S, et al. Among authors: pepe e. Int J Pediatr Otorhinolaryngol. 2007 Feb;71(2):247-55. doi: 10.1016/j.ijporl.2006.10.013. Epub 2006 Nov 20. Int J Pediatr Otorhinolaryngol. 2007. PMID: 17116334

5

[Current approaches in the treatment of gastroschisis].

De Grazia E, Acierno C, Pepe E, Curreri G, Cataliotti F. De Grazia E, et al. Among authors: pepe e. Minerva Pediatr. 1988 Dec;40(12):701-4. Minerva Pediatr. 1988. PMID: 2977635 Italian. No abstract available.

6

A heritable cause of cleft lip and palate--Van der Woude syndrome caused by a novel IRF6 mutation. Review of the literature and of the differential diagnosis.

Ferrero GB, Baldassarre G, Panza E, Valenzise M, Pippucci T, Mussa A, Pepe E, Seri M, Silengo MC. Ferrero GB, et al. Among authors: pepe e. Eur J Pediatr. 2010 Feb;169(2):223-8. doi: 10.1007/s00431-009-1011-3. Epub 2009 Jun 18. Eur J Pediatr. 2010. PMID: 19536562

7

Neonatal hepatoblastoma in a newborn with severe phenotype of Beckwith-Wiedemann syndrome.

Mussa A, Ferrero GB, Ceoloni B, Basso E, Chiesa N, De Crescenzo A, Pepe E, Silengo M, de Sanctis L. Mussa A, et al. Among authors: pepe e. Eur J Pediatr. 2011 Nov;170(11):1407-11. doi: 10.1007/s00431-011-1455-0. Epub 2011 Mar 30. Eur J Pediatr. 2011. PMID: 21448630

8

Complex cerebral malformation including Dandy-Walker in a newborn with trisomy 9 mosaicism.

Murru P, Coscia A, Martano C, Tibaldi M, Stefanini L, Pepe E, Battistoni G, Silengo M. Murru P, et al. Among authors: pepe e. Radiol Med. 2002 Mar;103(3):261-3. Radiol Med. 2002. PMID: 11976623 English, Italian. No abstract available.

9

Bilaterally cleft lip and bilateral thumb polydactyly with triphalangeal component in a patient with two de novo deletions of HSA 4q32 and 4q34 involving PDGFC, GRIA2, and FBXO8 genes.

Calcia A, Gai G, Di Gregorio E, Talarico F, Naretto VG, Migone N, Pepe E, Grosso E, Brusco A. Calcia A, et al. Among authors: pepe e. Am J Med Genet A. 2013 Oct;161A(10):2656-62. doi: 10.1002/ajmg.a.36146. Epub 2013 Aug 16. Am J Med Genet A. 2013. PMID: 24038848 Review.

10

[Acute appendicitis in childhood. Evaluation of a computerized diagnostic model].

Li Voti G, Pepe E, Acierno C, Pitruzzella E, Lima GC, Cataliotti F. Li Voti G, et al. Among authors: pepe e. Minerva Pediatr. 1986 Jun 30;38(11-12):447-50. Minerva Pediatr. 1986. PMID: 3526108 Italian. No abstract available.

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