Bosio S - Search Results

1

A new mutation trans to I278T cystathionine beta-synthase associated with Factor V Leiden causes mild homocystinuria but severe vascular disease.

Bosio S, Cavallero G, Brusa E, Alberti F, Camaschella C. Bosio S, et al. Thromb Haemost. 2001 Aug;86(2):716-7. Thromb Haemost. 2001. PMID: 11522031 No abstract available.

2

Epcr 23 bp insertion in a patient with severe progressive arterial disease: a dominant loss of function mutant in conditions of increased APC request?

Zecchina G, Bosio S, Brusa E, Rege-Cambrin G, Camaschella C. Zecchina G, et al. Among authors: bosio s. Br J Haematol. 2002 Dec;119(3):881-2. doi: 10.1046/j.1365-2141.2002.03870_6.x. Br J Haematol. 2002. PMID: 12437679 Free article. No abstract available.

3

Recurrent mutations in the iron regulatory element of L-ferritin in hereditary hyperferritinemia-cataract syndrome.

Cicilano M, Zecchina G, Roetto A, Bosio S, Infelise V, Stefani S, Mazza U, Camaschella C. Cicilano M, et al. Among authors: bosio s. Haematologica. 1999 Jun;84(6):489-92. Haematologica. 1999. PMID: 10366790

4

Hyperhomocysteinemia in patients with Cushing's syndrome.

Terzolo M, Allasino B, Bosio S, Brusa E, Daffara F, Ventura M, Aroasio E, Sacchetto G, Reimondo G, Angeli A, Camaschella C. Terzolo M, et al. Among authors: bosio s. J Clin Endocrinol Metab. 2004 Aug;89(8):3745-51. doi: 10.1210/jc.2004-0079. J Clin Endocrinol Metab. 2004. PMID: 15292300

5

Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome.

Girelli D, Bozzini C, Zecchina G, Tinazzi E, Bosio S, Piperno A, Ramenghi U, Peters J, Levi S, Camaschella C, Corrocher R. Girelli D, et al. Among authors: bosio s. Br J Haematol. 2001 Nov;115(2):334-40. doi: 10.1046/j.1365-2141.2001.03116.x. Br J Haematol. 2001. PMID: 11703332 Free article.

6

C29G in the iron-responsive element of L-ferritin: a new mutation associated with hyperferritinemia-cataract.

Bosio S, Campanella A, Gramaglia E, Porporato P, Longo F, Cremonesi L, Levi S, Camaschella C. Bosio S, et al. Blood Cells Mol Dis. 2004 Jul-Aug;33(1):31-4. doi: 10.1016/j.bcmd.2004.04.010. Blood Cells Mol Dis. 2004. PMID: 15223007

7

Variation in the phenotypic expression of C282Y hemochromatosis in an Italian family.

Bosio S, Zecchina G, Cicilano M, Roetto A, Salto AM, Camaschella C. Bosio S, et al. Haematologica. 1999 Feb;84(2):184-5. Haematologica. 1999. PMID: 10091421 No abstract available.

8

G20210A homozygosity in antiphospholipid syndrome secondary to systemic lupus erythematosus.

Sivera P, Bosio S, Bertero MT, Demaestri M, Mazza U, Camaschella C. Sivera P, et al. Among authors: bosio s. Haematologica. 2000 Jan;85(1):109-10. Haematologica. 2000. PMID: 10629608 No abstract available.

9

Haemochromatosis in patients with beta-thalassaemia trait.

Piperno A, Mariani R, Arosio C, Vergani A, Bosio S, Fargion S, Sampietro M, Girelli D, Fraquelli M, Conte D, Fiorelli G, Camaschella C. Piperno A, et al. Among authors: bosio s. Br J Haematol. 2000 Dec;111(3):908-14. Br J Haematol. 2000. PMID: 11122155 Free article.

10

Linkage to chromosome 1q in Greek families with juvenile hemochromatosis.

Papanikolaou G, Politou M, Roetto A, Bosio S, Sakelaropoulos N, Camaschella C, Loukopoulos D. Papanikolaou G, et al. Among authors: bosio s. Blood Cells Mol Dis. 2001 Jul-Aug;27(4):744-9. doi: 10.1006/bcmd.2001.0444. Blood Cells Mol Dis. 2001. PMID: 11778658

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

85 results

Search Page