Iolascon A - Search Results

1

Natural history of recessive inheritance of DMT1 mutations.

Iolascon A, Camaschella C, Pospisilova D, Piscopo C, Tchernia G, Beaumont C. Iolascon A, et al. J Pediatr. 2008 Jan;152(1):136-9. doi: 10.1016/j.jpeds.2007.08.041. J Pediatr. 2008. PMID: 18154916

2

Molecular pathology of inherited erythrocyte membrane disorders: hereditary spherocytosis and elliptocytosis.

Iolascon A, Miraglia del Giudice E, Camaschella C. Iolascon A, et al. Haematologica. 1992 Jan-Feb;77(1):60-72. Haematologica. 1992. PMID: 1356891 Review.

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

Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (16q23-qter).

Carella M, Stewart G, Ajetunmobi JF, Perrotta S, Grootenboer S, Tchernia G, Delaunay J, Totaro A, Zelante L, Gasparini P, Iolascon A. Carella M, et al. Among authors: iolascon a. Am J Hum Genet. 1998 Sep;63(3):810-6. doi: 10.1086/302024. Am J Hum Genet. 1998. PMID: 9718354 Free PMC article.

5

Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II).

Perrotta S, del Giudice EM, Carbone R, Servedio V, Schettini F Jr, Nobili B, Iolascon A. Perrotta S, et al. Among authors: iolascon a. J Pediatr. 2000 Apr;136(4):556-9. doi: 10.1016/s0022-3476(00)90026-x. J Pediatr. 2000. PMID: 10753261 Review.

6

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.

7

Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis.

Tchernia G, Delhommeau F, Perrotta S, Cynober T, Bader-Meunier B, Nobili B, Rohrlich P, Salomon JL, Sagot-Bevenot S, del Giudice EM, Delaunay J, DeMattia D, Schischmanoff PO, Mohandas N, Iolascon A; ESPHI working group on hemolytic anemias. Tchernia G, et al. Among authors: iolascon a. Hematol J. 2000;1(3):146-52. doi: 10.1038/sj.thj.6200022. Hematol J. 2000. PMID: 11920183

8

Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2).

Iolascon A, d'Apolito M, Servedio V, Cimmino F, Piga A, Camaschella C. Iolascon A, et al. Blood. 2006 Jan 1;107(1):349-54. doi: 10.1182/blood-2005-06-2477. Epub 2005 Sep 13. Blood. 2006. PMID: 16160008 Free article.

9

A novel R416C mutation in human DMT1 (SLC11A2) displays pleiotropic effects on function and causes microcytic anemia and hepatic iron overload.

Lam-Yuk-Tseung S, Camaschella C, Iolascon A, Gros P. Lam-Yuk-Tseung S, et al. Among authors: iolascon a. Blood Cells Mol Dis. 2006 May-Jun;36(3):347-54. doi: 10.1016/j.bcmd.2006.01.011. Epub 2006 Apr 3. Blood Cells Mol Dis. 2006. PMID: 16584902

10

Cytokine gene polymorphisms in Italian preterm infants: association between interleukin-10 -1082 G/A polymorphism and respiratory distress syndrome.

Capasso M, Avvisati RA, Piscopo C, Laforgia N, Raimondi F, de Angelis F, Iolascon A. Capasso M, et al. Among authors: iolascon a. Pediatr Res. 2007 Mar;61(3):313-7. doi: 10.1203/pdr.0b013e318030d108. Pediatr Res. 2007. PMID: 17314689

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