Farina V - Search Results

1

Geleophysic dysplasia: 7-year follow-up study of a patient with an intermediate form.

Titomanlio L, Della Casa R, Lecora M, Farina V, Sebastio G, Andria G, Parenti G. Titomanlio L, et al. Among authors: farina v. Am J Med Genet. 1999 Sep 3;86(1):82-5. Am J Med Genet. 1999. PMID: 10440835

2

Inv dup del (1)(pter-->q44::q44-->q42:) with the classical phenotype of trisomy 1q42-qter.

De Brasi D, Rossi E, Giglio S, D'Agostino A, Titomanlio L, Farina V, Andria G, Sebastio G. De Brasi D, et al. Among authors: farina v. Am J Med Genet. 2001 Nov 22;104(2):127-30. doi: 10.1002/ajmg.1589. Am J Med Genet. 2001. PMID: 11746042

3

Clinical variability of cardio-facio-cutaneous syndrome: report of two additional cases.

Ghezzi M, Parenti G, de Franchis R, Farina V, de Leva F, Guarino A, Canani RB, Strisciuglio P. Ghezzi M, et al. Among authors: farina v. Clin Genet. 1992 Oct;42(4):206-9. doi: 10.1111/j.1399-0004.1992.tb03239.x. Clin Genet. 1992. PMID: 1358488 Review.

4

Pulmonary manifestations of Gaucher disease: an increased risk for L444P homozygotes?

Santamaria F, Parenti G, Guidi G, Filocamo M, Strisciuglio P, Grillo G, Farina V, Sarnelli P, Rizzolo MG, Rotondo A, Andria G. Santamaria F, et al. Among authors: farina v. Am J Respir Crit Care Med. 1998 Mar;157(3 Pt 1):985-9. doi: 10.1164/ajrccm.157.3.9706057. Am J Respir Crit Care Med. 1998. PMID: 9517621

5

Echo-Doppler abnormalities in mucopolysaccharide storage diseases.

Farina V, de Leva F, Caso P, Scippa L, Parenti G, Strisciuglio P. Farina V, et al. Acta Paediatr. 1992 Sep;81(9):702-4. doi: 10.1111/j.1651-2227.1992.tb12339.x. Acta Paediatr. 1992. PMID: 1421914 No abstract available.

6

Prolonged Q-T interval syndrome presenting as idiopathic epilepsy.

Pignata C, Farina V, Andria G, Del Giudice E, Striano S, Adinolfi L. Pignata C, et al. Among authors: farina v. Neuropediatrics. 1983 Nov;14(4):235-6. doi: 10.1055/s-2008-1059585. Neuropediatrics. 1983. PMID: 6657011

7

Subtle alterations of cardiac performance in children with growth hormone deficiency: results of a two-year prospective, case-control study.

Capalbo D, Lo Vecchio A, Farina V, Spinelli L, Palladino A, Tiano C, Lettiero T, Lombardi G, Colao A, Salerno M. Capalbo D, et al. Among authors: farina v. J Clin Endocrinol Metab. 2009 Sep;94(9):3347-55. doi: 10.1210/jc.2008-2639. Epub 2009 Jul 7. J Clin Endocrinol Metab. 2009. PMID: 19584193

8

Studies on the pathogenesis of Costello syndrome.

Mancini GM, van Diggelen OP, Kleijer WJ, Di Rocco M, Farina V, Yuksel-Apak M, Kayserili H, Halley DJ. Mancini GM, et al. Among authors: farina v. J Med Genet. 2003 Apr;40(4):e37. doi: 10.1136/jmg.40.4.e37. J Med Genet. 2003. PMID: 12676910 Free PMC article. No abstract available.

9

Longitudinal assessment of cardiac status by echocardiographic evaluation of left ventricular diastolic function in thalassaemic children.

Fiorillo A, Farina V, D'Amore R, Scippa L, Cortese P, DeChiara C. Fiorillo A, et al. Among authors: farina v. Acta Paediatr. 2000 Apr;89(4):436-41. doi: 10.1080/080352500750028159. Acta Paediatr. 2000. PMID: 10830456

10

Myocardial dysfunction in two hypothyroid twins with thalassaemia major.

Fiorillo A, Farina V, DiMaio S, Ciriaco M, Nunziata L, Scippa L, D'Agostino N. Fiorillo A, et al. Among authors: farina v. Acta Paediatr Scand. 1989 May;78(3):455-7. doi: 10.1111/j.1651-2227.1989.tb11110.x. Acta Paediatr Scand. 1989. PMID: 2741689 No abstract available.

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