Iolascon A - Search Results

1

Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemia.

D'Apolito M, Marrone A, Servedio V, Vajro P, De Falco L, Iolascon A. D'Apolito M, et al. Among authors: iolascon a. Haematologica. 2007 Jan;92(1):133-4. doi: 10.3324/haematol.10585. Haematologica. 2007. PMID: 17229650 Free article.

2

(TA)8 allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndrome.

Iolascon A, Faienza MF, Centra M, Storelli S, Zelante L, Savoia A. Iolascon A, et al. Haematologica. 1999 Feb;84(2):106-9. Haematologica. 1999. PMID: 10091406

3

Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndromes.

Sampietro M, Iolascon A. Sampietro M, et al. Among authors: iolascon a. Haematologica. 1999 Feb;84(2):150-7. Haematologica. 1999. PMID: 10091414 Review.

4

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.

5

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

6

Two regions of deletion in 9p22- p24 in neuroblastoma are frequently observed in favorable tumors.

Giordani L, Iolascon A, Servedio V, Mazzocco K, Longo L, Tonini GP. Giordani L, et al. Among authors: iolascon a. Cancer Genet Cytogenet. 2002 May;135(1):42-7. doi: 10.1016/s0165-4608(01)00640-9. Cancer Genet Cytogenet. 2002. PMID: 12072202

7

Genes transcriptionally modulated by interferon alpha2a correlate with the cytokine activity.

Iolascon A, Volinia S, Borriello A, Giordani L, Moretti A, Servedio V, Maiorano N, Cucciolla V, Criniti V, Gasparini P, Indaco S, Della Ragione F. Iolascon A, et al. Haematologica. 2004 Sep;89(9):1046-53. Haematologica. 2004. PMID: 15377465

8

Spectrum of UGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlation.

Servedio V, d'Apolito M, Maiorano N, Minuti B, Torricelli F, Ronchi F, Zancan L, Perrotta S, Vajro P, Boschetto L, Iolascon A. Servedio V, et al. Among authors: iolascon a. Hum Mutat. 2005 Mar;25(3):325. doi: 10.1002/humu.9322. Hum Mutat. 2005. PMID: 15712364

9

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.

10

Kernicterus associated with hereditary spherocytosis and UGT1A1 promoter polymorphism.

Berardi A, Lugli L, Ferrari F, Gargano G, D'Apolito M, Marrone A, Iolascon A. Berardi A, et al. Among authors: iolascon a. Biol Neonate. 2006;90(4):243-6. doi: 10.1159/000093668. Epub 2006 May 30. Biol Neonate. 2006. PMID: 16735790

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