Schettini F - Search Results

1

A novel single-base mutation in the glucose 6-phosphate dehydrogenase gene is associated with chronic non-spherocytic haemolytic anaemia.

Filosa S, Cai W, Galanello R, Cao A, de Mattia D, Schettini F, Martini G. Filosa S, et al. Among authors: schettini f. Hum Genet. 1994 Nov;94(5):560-2. doi: 10.1007/BF00211027. Hum Genet. 1994. PMID: 7959695

2

Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for glucose-6-phosphate dehydrogenase mutations causing severe enzyme deficiency.

Filosa S, Giacometti N, Wangwei C, De Mattia D, Pagnini D, Alfinito F, Schettini F, Luzzatto L, Martini G. Filosa S, et al. Among authors: schettini f. Am J Hum Genet. 1996 Oct;59(4):887-95. Am J Hum Genet. 1996. PMID: 8808605 Free PMC article.

3

rhG-CSF in severe chronic neutropenia: successful intermittent treatment in three infants.

De Mattia D, Del Vecchio GC, Ferrante P, Schettini F. De Mattia D, et al. Among authors: schettini f. Pediatr Hematol Oncol. 1997 May-Jun;14(3):277-80. doi: 10.3109/08880019709009498. Pediatr Hematol Oncol. 1997. PMID: 9185213

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: schettini f. Haematologica. 1997 Nov-Dec;82(6):698-700. Haematologica. 1997. PMID: 9499670

5

Reconstitution of normal neutrophil function in chronic granulomatous disease by bone marrow transplantation.

Di Bartolomeo P, Di Girolamo G, Angrilli F, Schettini F, De Mattia D, Manzionna MM, Dragani A, Iacone A, Torlontano G. Di Bartolomeo P, et al. Among authors: schettini f. Bone Marrow Transplant. 1989 Nov;4(6):695-700. Bone Marrow Transplant. 1989. PMID: 2819288

6

Unbalanced coagulation-fibrinolysis potential during L-asparaginase therapy in children with acute lymphoblastic leukaemia.

Semeraro N, Montemurro P, Giordano P, Schettini F, Santoro N, De Mattia D, Giordano D, Conese M, Colucci M. Semeraro N, et al. Among authors: schettini f. Thromb Haemost. 1990 Aug 13;64(1):38-40. Thromb Haemost. 1990. PMID: 2274927

7

Characterisation of CAH alleles with non-radioactive DNA single strand conformation polymorphism analysis of the CYP21 gene.

Bobba A, Iolascon A, Giannattasio S, Albrizio M, Sinisi A, Prisco F, Schettini F, Marra E. Bobba A, et al. Among authors: schettini f. J Med Genet. 1997 Mar;34(3):223-8. doi: 10.1136/jmg.34.3.223. J Med Genet. 1997. PMID: 9132494 Free PMC article.

8

[The clinico-immunological evaluation of a bivalent vaccine against measles and rubella].

Schettini F, Manzionna MM, De Mattia D, Amendola F, Di Bitonto G. Schettini F, et al. Minerva Pediatr. 1990 Dec;42(12):531-6. Minerva Pediatr. 1990. PMID: 2087226 Italian.

9

Bone marrow transplantation for chronic granulomatous disease associated with cytochrome B deficiency.

Schettini F, De Mattia D, Manzionna MM, Seger RA, Fumarulo R, Torlontano G, Iacone A. Schettini F, et al. Pediatr Hematol Oncol. 1987;4(3):277-9. doi: 10.3109/08880018709141279. Pediatr Hematol Oncol. 1987. PMID: 3152933 No abstract available.

10

Lymphadenopathy syndrome and HIV infection in multitransfused beta-thalassemia child.

Schettini F, De Mattia D, Fumarola D, Pollice L. Schettini F, et al. Boll Ist Sieroter Milan. 1987;66(3):235-8. Boll Ist Sieroter Milan. 1987. PMID: 3435653

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

321 results

Search Page

Filters