Iolascon A - Search Results

1

Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibition.

Perrotta S, Nobili B, Rossi F, Criscuolo M, Iolascon A, Di Pinto D, Passaro I, Cennamo L, Oliva A, Della Ragione F. Perrotta S, et al. Among authors: iolascon a. Blood. 2002 Mar 15;99(6):2017-22. doi: 10.1182/blood.v99.6.2017. Blood. 2002. PMID: 11877274 Free article.

2

Alpha I/65 hereditary elliptocytosis in southern Italy: evidence for an African origin.

del Giudice EM, Ducluzeau MT, Alloisio N, Wilmotte R, Delaunay J, Perrotta S, Cutillo S, Iolascon A. del Giudice EM, et al. Among authors: iolascon a. Hum Genet. 1992 Jul;89(5):553-6. doi: 10.1007/BF00219183. Hum Genet. 1992. PMID: 1353056

3

Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis.

Cutillo S, Pinto L, Nobili B, Miraglia del Giudice E, Iolascon A. Cutillo S, et al. Among authors: iolascon a. Eur J Pediatr. 1992 Jan;151(1):35-7. doi: 10.1007/BF02073887. Eur J Pediatr. 1992. PMID: 1728542

4

Analysis of N-ras gene mutations in medulloblastomas by polymerase chain reaction and oligonucleotide probes in formalin-fixed, paraffin-embedded tissues.

Iolascon A, Lania A, Badiali M, Pession A, Saglio G, Giangaspero F, Miraglia del Giudice E, Perrotta S, Cutillo S. Iolascon A, et al. Med Pediatr Oncol. 1991;19(4):240-5. doi: 10.1002/mpo.2950190406. Med Pediatr Oncol. 1991. PMID: 2056968

5

Clinical and biochemical study of thalassemia intermedia in Campania (southern Italy).

Iolascon A, Pinto L, Nobili B, Lania A, Iafusco D, Miraglia del Giudice E, Matarese SM, Salvati P, Cutillo S. Iolascon A, et al. Birth Defects Orig Artic Ser. 1987;23(5A):281-5. Birth Defects Orig Artic Ser. 1987. PMID: 3689908 No abstract available.

6

Increased membrane-protein methylation in hereditary spherocytosis. A marker of cytoskeletal disarray.

Ingrosso D, D'Angelo S, Perna AF, Iolascon A, Miraglia del Giudice E, Perrotta S, Zappia V, Galletti P. Ingrosso D, et al. Among authors: iolascon a. Eur J Biochem. 1995 Mar 15;228(3):894-8. doi: 10.1111/j.1432-1033.1995.tb20337.x. Eur J Biochem. 1995. PMID: 7737191 Free article.

7

Spectrin Anastasia (alpha I/78): a new spectrin variant (alpha 45 Arg-->Thr) with moderate elliptocytogenic potential.

Perrotta S, Iolascon A, De Angelis F, Pagano L, Colonna G, Cutillo S, Miraglia del Giudice E. Perrotta S, et al. Among authors: iolascon a. Br J Haematol. 1995 Apr;89(4):933-6. Br J Haematol. 1995. PMID: 7772539

8

Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis.

Miraglia del Giudice E, Iolascon A, Pinto L, Nobili B, Perrotta S. Miraglia del Giudice E, et al. Among authors: iolascon a. Br J Haematol. 1994 Sep;88(1):52-5. doi: 10.1111/j.1365-2141.1994.tb04976.x. Br J Haematol. 1994. PMID: 7803256

9

Molecular heterogeneity of hereditary elliptocytosis in Italy.

Miraglia del Giudice E, Perrotta S, Sannino E, De Angelis F, Nobili B, Iolascon A. Miraglia del Giudice E, et al. Among authors: iolascon a. Haematologica. 1994 Sep-Oct;79(5):400-5. Haematologica. 1994. PMID: 7843625

10

5'-Deoxy-5'-methylthioadenosine phosphorylase and p16INK4 deficiency in multiple tumor cell lines.

Della Ragione F, Russo G, Oliva A, Mastropietro S, Mancini A, Borrelli A, Casero RA, Iolascon A, Zappia V. Della Ragione F, et al. Among authors: iolascon a. Oncogene. 1995 Mar 2;10(5):827-33. Oncogene. 1995. PMID: 7898924

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