Olivieri O - Search Results

1

Atypical hemolytic uremic syndrome: Unique clinical presentation linked to rare CFHR5 mutation.

Menotti S, Donini M, Pessolano G, Tiro L, Cantini M, Croce J, Morandi M, Mazzi F, Donadello K, Olivieri O, Dima F, De Marchi S, Gambaro G, Polati E, De Franceschi L. Menotti S, et al. Among authors: olivieri o. EJHaem. 2021 Sep 14;2(4):838-841. doi: 10.1002/jha2.288. eCollection 2021 Nov. EJHaem. 2021. PMID: 35845199 Free PMC article. No abstract available.

2

Molecular basis for the recently described hereditary hyperferritinemia-cataract syndrome: a mutation in the iron-responsive element of ferritin L-subunit gene (the "Verona mutation").

Girelli D, Corrocher R, Bisceglia L, Olivieri O, De Franceschi L, Zelante L, Gasparini P. Girelli D, et al. Among authors: olivieri o. Blood. 1995 Dec 1;86(11):4050-3. Blood. 1995. PMID: 7492760 Free article.

3

Oxidative damage and erythrocyte membrane transport abnormalities in thalassemias.

Olivieri O, De Franceschi L, Capellini MD, Girelli D, Corrocher R, Brugnara C. Olivieri O, et al. Blood. 1994 Jul 1;84(1):315-20. Blood. 1994. PMID: 8018927 Free article.

4

Red blood cell cation transports in uraemic anaemia: evidence for an increased K/Cl co-transport activity. Effects of dialysis and erythropoietin treatment.

De Franceschi L, Olivieri O, Girelli D, Lupo A, Bernich P, Corrocher R. De Franceschi L, et al. Among authors: olivieri o. Eur J Clin Invest. 1995 Oct;25(10):762-8. doi: 10.1111/j.1365-2362.1995.tb01955.x. Eur J Clin Invest. 1995. PMID: 8557063

5

Deficiency of Src family kinases Fgr and Hck results in activation of erythrocyte K/Cl cotransport.

De Franceschi L, Fumagalli L, Olivieri O, Corrocher R, Lowell CA, Berton G. De Franceschi L, et al. Among authors: olivieri o. J Clin Invest. 1997 Jan 15;99(2):220-7. doi: 10.1172/JCI119150. J Clin Invest. 1997. PMID: 9005990 Free PMC article.

6

Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: effects of different membrane protein defects.

De Franceschi L, Olivieri O, Miraglia del Giudice E, Perrotta S, Sabato V, Corrocher R, Iolascon A. De Franceschi L, et al. Among authors: olivieri o. Am J Hematol. 1997 Jul;55(3):121-8. doi: 10.1002/(sici)1096-8652(199707)55:3<121::aid-ajh1>3.0.co;2-u. Am J Hematol. 1997. PMID: 9256290 Free article.

7

Decreased band 3 anion transport activity and band 3 clusterization in congenital dyserythropoietic anemia type II.

De Franceschi L, Turrini F, del Giudice EM, Perrotta S, Olivieri O, Corrocher R, Mannu F, Iolascon A. De Franceschi L, et al. Among authors: olivieri o. Exp Hematol. 1998 Aug;26(9):869-73. Exp Hematol. 1998. PMID: 9694508

8

Deferiprone therapy in homozygous human beta-thalassemia removes erythrocyte membrane free iron and reduces KCl cotransport activity.

de Franceschi L, Shalev O, Piga A, Collell M, Olivieri O, Corrocher R, Hebbel RP, Brugnara C. de Franceschi L, et al. Among authors: olivieri o. J Lab Clin Med. 1999 Jan;133(1):64-9. doi: 10.1053/lc.1999.v133.a94241. J Lab Clin Med. 1999. PMID: 10385483 Clinical Trial.

9

Erythrocyte aging in neurodegenerative disorders.

De Franceschi L, Olivieri O, Corrocher R. De Franceschi L, et al. Among authors: olivieri o. Cell Mol Biol (Noisy-le-grand). 2004 Mar;50(2):179-85. Cell Mol Biol (Noisy-le-grand). 2004. PMID: 15095788 Review.

10

Deoxygenation affects tyrosine phosphoproteome of red cell membrane from patients with sickle cell disease.

Siciliano A, Turrini F, Bertoldi M, Matte A, Pantaleo A, Olivieri O, De Franceschi L. Siciliano A, et al. Among authors: olivieri o. Blood Cells Mol Dis. 2010 Apr 15;44(4):233-42. doi: 10.1016/j.bcmd.2010.02.007. Epub 2010 Mar 4. Blood Cells Mol Dis. 2010. PMID: 20206558

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