Iolascon A - Search Results

1

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.

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

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.

4

Resistance to activated protein C as a risk factor of stroke in a thalassemic patient.

Giordano P, Sabato V, Schettini F, De Mattia D, Iolascon A. Giordano P, et al. Among authors: iolascon a. Haematologica. 1997 Nov-Dec;82(6):698-700. Haematologica. 1997. PMID: 9499670

5

Hereditary spherocytosis: from clinical to molecular defects.

Iolascon A, Miraglia del Giudice E, Perrotta S, Alloisio N, Morlé L, Delaunay J. Iolascon A, et al. Haematologica. 1998 Mar;83(3):240-57. Haematologica. 1998. PMID: 9573679 Review.

6

Decision making at the bedside: diagnosis of hereditary spherocytosis in a transfused infant.

Miraglia del Giudice E, Perrotta S, Lombardi C, Iolascon A. Miraglia del Giudice E, et al. Among authors: iolascon a. Haematologica. 1998 Apr;83(4):347-9. Haematologica. 1998. PMID: 9592985

7

Expression of cell cycle regulatory genes in chronic myelogenous leukemia.

Iolascon A, Della Ragione F, Giordani L, Serra A, Saglio G, Faienza MF. Iolascon A, et al. Haematologica. 1998 Sep;83(9):771-7. Haematologica. 1998. PMID: 9825572

8

Gilbert's syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonates.

Iolascon A, Faienza MF, Perrotta S, Meloni GF, Ruggiu G, del Giudice EM. Iolascon A, et al. Haematologica. 1999 Feb;84(2):99-102. Haematologica. 1999. PMID: 10091404 Clinical Trial.

9

(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

10

Homozygous prothrombin gene mutation and ischemic cerebrovascular disease: a case report.

Giordano P, De Lucia D, Coppola B, Iolascon A. Giordano P, et al. Among authors: iolascon a. Acta Haematol. 1999;102(2):101-3. doi: 10.1159/000040979. Acta Haematol. 1999. PMID: 10529515

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