Iolascon A - Search Results

1

Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian population.

Russo R, Gambale A, Esposito MR, Serra ML, Troiano A, De Maggio I, Capasso M, Luzzatto L, Delaunay J, Tamary H, Iolascon A. Russo R, et al. Among authors: iolascon a. Am J Hematol. 2011 Sep;86(9):727-32. doi: 10.1002/ajh.22096. Am J Hematol. 2011. PMID: 21850656 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 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

4

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.

5

Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide search.

Gasparini P, Miraglia del Giudice E, Delaunay J, Totaro A, Granatiero M, Melchionda S, Zelante L, Iolascon A. Gasparini P, et al. Among authors: iolascon a. Am J Hum Genet. 1997 Nov;61(5):1112-6. doi: 10.1086/301609. Am J Hum Genet. 1997. PMID: 9345103 Free PMC article.

6

Hereditary dehydrated and overhydrated stomatocytosis: recent advances.

Delaunay J, Stewart G, Iolascon A. Delaunay J, et al. Among authors: iolascon a. Curr Opin Hematol. 1999 Mar;6(2):110-4. doi: 10.1097/00062752-199903000-00009. Curr Opin Hematol. 1999. PMID: 10088641 Review.

7

Suppression of CDA II expression in a homozygote.

Beauchamp-Nicoud A, Schischmanoff PO, Alloisio N, Boivin P, Parsons SF, Mielot F, Tchernia G, Legrand A, Miraglia Del Giudice E, Gasparini P, Iolascon A, Wickramasinghe SN, Delaunay J. Beauchamp-Nicoud A, et al. Among authors: iolascon a. Br J Haematol. 1999 Sep;106(4):948-53. doi: 10.1046/j.1365-2141.1999.01626.x. Br J Haematol. 1999. PMID: 10519996 Free article.

8

Geographic distribution of CDA-II: did a founder effect operate in Southern Italy?

Iolascon A, Servedio V, Carbone R, Totaro A, Carella M, Perrotta S, Wickramasinghe SN, Delaunay J, Heimpel H, Gasparini P. Iolascon A, et al. Haematologica. 2000 May;85(5):470-4. Haematologica. 2000. PMID: 10800161

9

The congenital dyserythropoietic anaemias.

Delaunay J, Iolascon A. Delaunay J, et al. Among authors: iolascon a. Baillieres Best Pract Res Clin Haematol. 1999 Dec;12(4):691-705. doi: 10.1053/beha.1999.0048. Baillieres Best Pract Res Clin Haematol. 1999. PMID: 10895259 Review.

10

Natural history of congenital dyserythropoietic anemia type II.

Iolascon A, Delaunay J, Wickramasinghe SN, Perrotta S, Gigante M, Camaschella C. Iolascon A, et al. Blood. 2001 Aug 15;98(4):1258-60. doi: 10.1182/blood.v98.4.1258. Blood. 2001. PMID: 11493480 Free article.

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