Romano V - Search Results

1

Congenital dyserythropoietic anemia type II associated with G6PD Seattle in a Sicilian child.

Gangarossa S, Romano V, Miraglia del Giudice E, Perrotta S, Iolascon A, Schiliro G. Gangarossa S, et al. Among authors: romano v. Acta Haematol. 1995;93(1):36-9. doi: 10.1159/000204087. Acta Haematol. 1995. PMID: 7725848

2

Micromegakaryocytes in a patient with partial deletion of the long arm of chromosome 11 [del(11)(q24.2qter)] and chronic thrombocytopenic purpura.

Gangarossa S, Mattina T, Romano V, Milana G, Mollica F, Schilirò G. Gangarossa S, et al. Among authors: romano v. Am J Med Genet. 1996 Mar 15;62(2):120-3. doi: 10.1002/(SICI)1096-8628(19960315)62:2<120::AID-AJMG4>3.0.CO;2-#. Am J Med Genet. 1996. PMID: 8882392

3

Liver involvement in white patients with sickle-cell disease.

Samperi P, Consalvo C, Romano V, Gelardi S, Di Bella D, Schilirò G. Samperi P, et al. Among authors: romano v. Arch Pediatr Adolesc Med. 1996 Nov;150(11):1177-80. doi: 10.1001/archpedi.1996.02170360067011. Arch Pediatr Adolesc Med. 1996. PMID: 8904859

4

Low serum levels of interleukin-6 in children with post-infective acute thrombocytopenic purpura.

Gangarossa S, Romano V, Munda SE, Sciotto A, Schilirò G. Gangarossa S, et al. Among authors: romano v. Eur J Haematol. 1995 Aug;55(2):117-20. doi: 10.1111/j.1600-0609.1995.tb01820.x. Eur J Haematol. 1995. PMID: 7628586

5

Efficacy of oral administration of high-dose cobamamide in a patient with Imerslund-Gräsbeck syndrome.

Gangarossa S, Romano V, Schilirò G. Gangarossa S, et al. Among authors: romano v. Pediatr Hematol Oncol. 1996 Jul-Aug;13(4):387-9. doi: 10.3109/08880019609030846. Pediatr Hematol Oncol. 1996. PMID: 8837146 No abstract available.

6

A mild form of Hb S-beta-thalassemia syndrome is assured in Sicilian patients by beta+mutant IVS-I nt 6(T-->C).

Mirabile E, Testa R, Samperi P, Consalvo C, Romano V, Schilirò G. Mirabile E, et al. Among authors: romano v. Eur J Haematol. 1997 Jan;58(1):67-9. doi: 10.1111/j.1600-0609.1997.tb01412.x. Eur J Haematol. 1997. PMID: 9020376 No abstract available.

7

RFLP analysis in 5 Sicilian families with the fragile X syndrome.

Romano V, Mascali G, Chiavetta V, Ragusa RM, Barletta C, Romano C, Mollica F, Mattina T, Gross A, Brown WT, et al. Romano V, et al. Among authors: romano c. Am J Med Genet. 1991 Feb-Mar;38(2-3):347-8. doi: 10.1002/ajmg.1320380236. Am J Med Genet. 1991. PMID: 1673309 No abstract available.

8

Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenylalaninemia in southern Europe.

Guldberg P, Romano V, Ceratto N, Bosco P, Ciuna M, Indelicato A, Mollica F, Meli C, Giovannini M, Riva E, et al. Guldberg P, et al. Among authors: romano v. Hum Mol Genet. 1993 Oct;2(10):1703-7. doi: 10.1093/hmg/2.10.1703. Hum Mol Genet. 1993. PMID: 8268925

9

Eight new mutations of the phenylalanine hydroxylase gene in Italian patients with hyperphenylalaninemia.

Bosco P, Cali F, Meli C, Mollica F, Zammarchi E, Cerone R, Vanni C, Palillo L, Greco D, Romano V. Bosco P, et al. Among authors: romano v. Hum Mutat. 1998;11(3):240-3. doi: 10.1002/(SICI)1098-1004(1998)11:3<240::AID-HUMU9>3.0.CO;2-L. Hum Mutat. 1998. PMID: 9521426

10

PAH deficiency in Italy: correlation of genotype with phenotype in the Sicilian population.

Romano V, Guldberg P, Güttler F, Meli C, Mollica F, Pavone L, Giovannini M, Riva E, Biasucci G, Luotti D, Palillo L, Calí F, Ceratto N, Anello G, Bosco P. Romano V, et al. J Inherit Metab Dis. 1996;19(1):15-24. doi: 10.1007/BF01799343. J Inherit Metab Dis. 1996. PMID: 8830172

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