Nobili B - Search Results

1

Clinical and biochemical study of thalassemia intermedia in Campania (southern Italy).

Iolascon A, Pinto L, Nobili B, Lania A, Iafusco D, Miraglia del Giudice E, Matarese SM, Salvati P, Cutillo S. Iolascon A, et al. Among authors: nobili b. Birth Defects Orig Artic Ser. 1987;23(5A):281-5. Birth Defects Orig Artic Ser. 1987. PMID: 3689908 No abstract available.

2

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

3

Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis.

Cutillo S, Pinto L, Nobili B, Miraglia del Giudice E, Iolascon A. Cutillo S, et al. Among authors: nobili b. Eur J Pediatr. 1992 Jan;151(1):35-7. doi: 10.1007/BF02073887. Eur J Pediatr. 1992. PMID: 1728542

4

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

5

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

6

[Alpha thalassemia in Campania: results of a survey of 319 newborn infants].

Pinto L, Esposito L, Vitale R, Cicale F, Scarano G, Nobili B. Pinto L, et al. Among authors: nobili b. Pediatria (Napoli). 1978 Dec 31;86(4):637-45. Pediatria (Napoli). 1978. PMID: 375183 Review. Italian. No abstract available.

7

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

8

[Bart's hemoglobin in newborn infants of Campania].

Iolascon A, Nobili B, Pinto L, Pepe A, Pisanti MA, Picardi L, Iolascon G. Iolascon A, et al. Among authors: nobili b. Pediatria (Napoli). 1982 Sep 30;90(3):339-41. Pediatria (Napoli). 1982. PMID: 7155705 Italian. No abstract available.

9

Flow-cytometric analysis of erythrocytes and reticulocytes in congenital dyserythropoietic anaemia type II (CDA II): value in differential diagnosis with hereditary spherocytosis.

Danise P, Amendola G, Nobili B, Perrotta S, Miraglia Del Giudice E, Matarese SM, Iolascon A, Brugnara C. Danise P, et al. Among authors: nobili b. Clin Lab Haematol. 2001 Feb;23(1):7-13. doi: 10.1046/j.1365-2257.2001.00354.x. Clin Lab Haematol. 2001. PMID: 11422224

10

[Glycerol test in thalassemia diagnosis (author's transl)].

Iolascon A, Nobili B, Pinto L, Pisanti MA, Visone C. Iolascon A, et al. Among authors: nobili b. Pediatria (Napoli). 1982 Mar 31;90(1):35-43. Pediatria (Napoli). 1982. PMID: 7110840 Italian. No abstract available.

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