Olivieri O - Search Results

1

Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events.

Patel RS, Schmidt AF, Tragante V, McCubrey RO, Holmes MV, Howe LJ, Direk K, Åkerblom A, Leander K, Virani SS, Kaminski KA, Muehlschlegel JD, Dubé MP, Allayee H, Almgren P, Alver M, Baranova EV, Behlouli H, Boeckx B, Braund PS, Breitling LP, Delgado G, Duarte NE, Dufresne L, Eriksson N, Foco L, Gijsberts CM, Gong Y, Hartiala J, Heydarpour M, Hubacek JA, Kleber M, Kofink D, Kuukasjärvi P, Lee VV, Leiherer A, Lenzini PA, Levin D, Lyytikäinen LP, Martinelli N, Mons U, Nelson CP, Nikus K, Pilbrow AP, Ploski R, Sun YV, Tanck MWT, Tang WHW, Trompet S, van der Laan SW, van Setten J, Vilmundarson RO, Viviani Anselmi C, Vlachopoulou E, Boerwinkle E, Briguori C, Carlquist JF, Carruthers KF, Casu G, Deanfield J, Deloukas P, Dudbridge F, Fitzpatrick N, Gigante B, James S, Lokki ML, Lotufo PA, Marziliano N, Mordi IR, Muhlestein JB, Newton Cheh C, Pitha J, Saely CH, Samman-Tahhan A, Sandesara PB, Teren A, Timmis A, Van de Werf F, Wauters E, Wilde AAM, Ford I, Stott DJ, Algra A, Andreassi MG, Ardissino D, Arsenault BJ, Ballantyne CM, Bergmeijer TO, Bezzina CR, Body SC, Bogaty P, de Borst GJ, Brenner H, Burkhardt R, Carpeggiani C, Condorelli G, Cooper-DeHoff RM, Cresci S, de Faire U, Doughty RN, D… See abstract for full author list ➔ Patel RS, et al. Among authors: olivieri o. Circ Genom Precis Med. 2019 Apr;12(4):e002471. doi: 10.1161/CIRCGEN.119.002471. Epub 2019 Mar 21. Circ Genom Precis Med. 2019. PMID: 30897348 Free PMC article.

2

Red blood cell molecular abnormalities in non haematological diseases.

De Sandre G, Girelli D, Olivieri O. De Sandre G, et al. Among authors: olivieri o. Haematologica. 1990 Sep-Oct;75(5):447-53. Haematologica. 1990. PMID: 1965832 Review.

3

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.

4

Differences in body mass index and smoking habit between untreated essential hypertensive patients with or without altered blood pressure circadian rhythm.

Russo C, Olivieri O, Girelli D, Stanzial AM, Azzini M, Corrocher R. Russo C, et al. Among authors: olivieri o. J Hypertens Suppl. 1993 Dec;11(5):S298-9. J Hypertens Suppl. 1993. PMID: 8158394 No abstract available.

5

Delayed multiorgan non-neoplastic damage after exposure to radiotherapy in infancy.

Olivieri O, Girelli D, Russo C, Nardelli E, Corrocher R. Olivieri O, et al. Eur J Med. 1993 Jan;2(1):58-9. Eur J Med. 1993. PMID: 8258008 No abstract available.

6

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

7

Selenium, zinc, and thyroid hormones in healthy subjects: low T3/T4 ratio in the elderly is related to impaired selenium status.

Olivieri O, Girelli D, Stanzial AM, Rossi L, Bassi A, Corrocher R. Olivieri O, et al. Biol Trace Elem Res. 1996 Jan;51(1):31-41. doi: 10.1007/BF02790145. Biol Trace Elem Res. 1996. PMID: 8834378

8

Relationships between serum uric acid and lipids in healthy subjects.

Russo C, Olivieri O, Girelli D, Guarini P, Corrocher R. Russo C, et al. Among authors: olivieri o. Prev Med. 1996 Sep-Oct;25(5):611-6. doi: 10.1006/pmed.1996.0096. Prev Med. 1996. PMID: 8888330

9

Influences of lipid and non-lipid nutritional parameters on factor VII coagulant activity in normal subjects: the Nove study.

Girelli D, Olivieri O, Arigliano PL, Guarini P, Bassi A, Corrocher R. Girelli D, et al. Among authors: olivieri o. Eur J Clin Invest. 1996 Mar;26(3):199-204. doi: 10.1046/j.1365-2362.1996.117265.x. Eur J Clin Invest. 1996. PMID: 8904348

10

Hereditary hyperferritinemia-cataract syndrome caused by a 29-base pair deletion in the iron responsive element of ferritin L-subunit gene.

Girelli D, Corrocher R, Bisceglia L, Olivieri O, Zelante L, Panozzo G, Gasparini P. Girelli D, et al. Among authors: olivieri o. Blood. 1997 Sep 1;90(5):2084-8. Blood. 1997. PMID: 9292547 Free article.

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