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Items: 8

1.

A Damage Sensor Associated with the Cuticle Coordinates Three Core Environmental Stress Responses in Caenorhabditis elegans.

Dodd W, Tang L, Lone JC, Wimberly K, Wu CW, Consalvo C, Wright JE, Pujol N, Choe KP.

Genetics. 2018 Apr;208(4):1467-1482. doi: 10.1534/genetics.118.300827. Epub 2018 Feb 27.

2.

[Leishmaniasis in a splenectomized thalassodrepanocytic young adult].

Pavone P, Giugno GR, Luca G, Samperi P, Consalvo C, Lucenti C.

Minerva Pediatr. 2005 Oct;57(5):325-8. Italian.

PMID:
16205619
3.

A mild form of Hb S-beta-thalassemia syndrome is assured in Sicilian patients by beta+mutant IVS-I nt 6(T-->C)

Mirabile E, Testa R, Samperi P, Consalvo C, Romano V, Schilirò G.

Eur J Haematol. 1997 Jan;58(1):67-9. No abstract available.

PMID:
9020376
4.

Liver involvement in white patients with sickle-cell disease.

Samperi P, Consalvo C, Romano V, Gelardi S, Di Bella D, Schilirò G.

Arch Pediatr Adolesc Med. 1996 Nov;150(11):1177-80.

PMID:
8904859
5.

Association of Hb S/Hb lepore and delta beta-thalassemia/Hb lepore in Sicilian patients: review of the presence of Hb lepore in Sicily.

Mirabile E, Testa R, Consalvo C, Dickerhoff R, Schilirò G.

Eur J Haematol. 1995 Aug;55(2):126-30.

PMID:
7543057
6.

Growth and development in white patients with sickle cell diseases.

Caruso-Nicoletti M, Mancuso M, Spadaro G, Samperi P, Consalvo C, Schilirò G.

Am J Pediatr Hematol Oncol. 1992 Nov;14(4):285-8.

PMID:
1280913
7.

Iron status in white sickle cell disease patients.

Russo-Mancuso G, Samperi P, Gangarossa S, Consalvo C, Schilirò G.

Eur J Haematol. 1992 Apr;48(4):232-3. No abstract available.

PMID:
1592104
8.

Clinical, hematological, and molecular features in Sicilians with sickle cell disease.

Schilirò G, Samperi P, Consalvo C, Gangarossa S, Testa R, Miraglia V, Lo Nigro L.

Hemoglobin. 1992;16(6):469-80.

PMID:
1487418

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