Iolascon A - Search Results

1

Mutational spectrum in congenital dyserythropoietic anemia type II: identification of 19 novel variants in SEC23B gene.

Russo R, Esposito MR, Asci R, Gambale A, Perrotta S, Ramenghi U, Forni GL, Uygun V, Delaunay J, Iolascon A. Russo R, et al. Among authors: iolascon a. Am J Hematol. 2010 Dec;85(12):915-20. doi: 10.1002/ajh.21866. Am J Hematol. 2010. PMID: 20941788 Free PMC 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

Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases.

Iolascon A, Miraglia del Giudice E, Camaschella C, Pinto L, Nobili B, Perrotta S, Cutillo S. Iolascon A, et al. Br J Haematol. 1991 Aug;78(4):551-4. doi: 10.1111/j.1365-2141.1991.tb04487.x. Br J Haematol. 1991. PMID: 1832935

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

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: iolascon a. Acta Haematol. 1995;93(1):36-9. doi: 10.1159/000204087. Acta Haematol. 1995. PMID: 7725848

6

Rapid detection of medium chain acyl-CoA dehydrogenase gene mutations by non-radioactive, single strand conformation polymorphism minigels.

Iolascon A, Parrella T, Perrotta S, Guardamagna O, Coates PM, Sartore M, Surrey S, Fortina P. Iolascon A, et al. J Med Genet. 1994 Jul;31(7):551-4. doi: 10.1136/jmg.31.7.551. J Med Genet. 1994. PMID: 7966191 Free PMC article.

7

Mild elliptocytosis associated with the alpha 34 Arg-->Trp mutation in spectrin Genova (alpha I/74).

Perrotta S, Miraglia del Giudice E, Alloisio N, Sciarratta G, Pinto L, Delaunay J, Cutillo S, Iolascon A. Perrotta S, et al. Among authors: iolascon a. Blood. 1994 Jun 1;83(11):3346-9. Blood. 1994. PMID: 8193371 Free article.

8

Ankyrin Napoli: a de novo deletional frameshift mutation in exon 16 of ankyrin gene (ANK1) associated with spherocytosis.

del Giudice EM, Hayette S, Bozon M, Perrotta S, Alloisio N, Vallier A, Iolascon A, Delaunay J, Morlé L. del Giudice EM, et al. Among authors: iolascon a. Br J Haematol. 1996 Jun;93(4):828-34. doi: 10.1046/j.1365-2141.1996.d01-1746.x. Br J Haematol. 1996. PMID: 8703812

9

Congenital dyserythropoietic anemia type II: molecular basis and clinical aspects.

Iolascon A, D'Agostaro G, Perrotta S, Izzo P, Tavano R, Miraglia del Giudice B. Iolascon A, et al. Haematologica. 1996 Nov-Dec;81(6):543-59. Haematologica. 1996. PMID: 9009444 Review.

10

Novel band 3 variants (bands 3 Foggia, Napoli I and Napoli II) associated with hereditary spherocytosis and band 3 deficiency: status of the D38A polymorphism within the EPB3 locus.

Miraglia del Giudice E, Vallier A, Maillet P, Perrotta S, Cutillo S, Iolascon A, Tanner MJ, Delaunay J, Alloisio N. Miraglia del Giudice E, et al. Among authors: iolascon a. Br J Haematol. 1997 Jan;96(1):70-6. doi: 10.1046/j.1365-2141.1997.8732504.x. Br J Haematol. 1997. PMID: 9012689 Free article.

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