Nobili B - Search Results

1

Clinical and molecular evaluation of non-dominant hereditary spherocytosis.

Miraglia del Giudice E, Nobili B, Francese M, D'Urso L, Iolascon A, Eber S, Perrotta S. Miraglia del Giudice E, et al. Among authors: nobili b. Br J Haematol. 2001 Jan;112(1):42-7. doi: 10.1046/j.1365-2141.2001.02501.x. Br J Haematol. 2001. PMID: 11167781 Free article.

2

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. Among authors: nobili b. Br J Haematol. 1991 Aug;78(4):551-4. doi: 10.1111/j.1365-2141.1991.tb04487.x. Br J Haematol. 1991. PMID: 1832935

3

Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis.

Miraglia del Giudice E, Iolascon A, Pinto L, Nobili B, Perrotta S. Miraglia del Giudice E, et al. Among authors: nobili b. Br J Haematol. 1994 Sep;88(1):52-5. doi: 10.1111/j.1365-2141.1994.tb04976.x. Br J Haematol. 1994. PMID: 7803256

4

Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotype.

Miraglia del Giudice E, Perrotta S, Nobili B, Pinto L, Cutillo L, Iolascon A. Miraglia del Giudice E, et al. Among authors: nobili b. Br J Haematol. 1993 Nov;85(3):553-7. doi: 10.1111/j.1365-2141.1993.tb03347.x. Br J Haematol. 1993. PMID: 8136278

5

Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele.

Miraglia del Giudice E, Francese M, Polito R, Nobili B, Iolascon A, Perrotta S. Miraglia del Giudice E, et al. Among authors: nobili b. Haematologica. 1997 May-Jun;82(3):332-3. Haematologica. 1997. PMID: 9234582

6

High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis.

Miraglia del Giudice E, Francese M, Nobili B, Morlé L, Cutillo S, Delaunay J, Perrotta S. Miraglia del Giudice E, et al. Among authors: nobili b. J Pediatr. 1998 Jan;132(1):117-20. doi: 10.1016/s0022-3476(98)70495-0. J Pediatr. 1998. PMID: 9470011

7

Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency.

Miraglia del Giudice E, Lombardi C, Francese M, Nobili B, Conte ML, Amendola G, Cutillo S, Iolascon A, Perrotta S. Miraglia del Giudice E, et al. Among authors: nobili b. Br J Haematol. 1998 May;101(2):251-4. doi: 10.1046/j.1365-2141.1998.00688.x. Br J Haematol. 1998. PMID: 9609518 Free article.

8

Molecular heterogeneity of hereditary elliptocytosis in Italy.

Miraglia del Giudice E, Perrotta S, Sannino E, De Angelis F, Nobili B, Iolascon A. Miraglia del Giudice E, et al. Among authors: nobili b. Haematologica. 1994 Sep-Oct;79(5):400-5. Haematologica. 1994. PMID: 7843625

9

Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis.

del Giudice EM, Perrotta S, Nobili B, Specchia C, d'Urzo G, Iolascon A. del Giudice EM, et al. Among authors: nobili b. Blood. 1999 Oct 1;94(7):2259-62. Blood. 1999. PMID: 10498597 Free article.

10

Reversible erythrocyte skeleton destabilization is modulated by beta-spectrin phosphorylation in childhood leukemia.

Perrotta S, del Giudice EM, Iolascon A, De Vivo M, Di Pinto D, Cutillo S, Nobili B. Perrotta S, et al. Among authors: nobili b. Leukemia. 2001 Mar;15(3):440-4. doi: 10.1038/sj.leu.2402047. Leukemia. 2001. PMID: 11237068

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