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Revue Des Maladies Respiratoires|January 1, 1989
[Effect of a single dose of nifedipine on the CO transfer capacity in patients with scleroderma]E Orvoen-Frija, M F Dore, J N Fiessinger, et al.
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles|September 19, 1977
[Serological identification of an antigen associated with acute lymphoid leukemia]C Guibout, J F Dore, L Marholev, et al.
Carcinogenesis|May 1, 1992
Tumorigenic activity of a rearranged c-myc gene from a human T-cell leukemia lineD Petroni, P Comi, B Giglioni, et al.
Blood|February 15, 1990
A new hereditary persistence of fetal hemoglobin deletion has the breakpoint within the 3' beta-globin gene enhancerC Camaschella, A Serra, E Gottardi, et al.
Human Pathology|June 1, 1997
Microsatellite instability in KSHV/HHV-8 positive body-cavity-based lymphomaG Gaidano, C Pastore, A Gloghini, et al.
Leukemia|October 26, 2002
Alterations of the FLT3 gene in acute promyelocytic leukemia: association with diagnostic characteristics and analysis of clinical outcome in patients treated with the Italian AIDA protocolN I Noguera, M Breccia, M Divona, et al.
Cancer Research|July 15, 1997
Infant acute leukemias show the same biased distribution of ALL1 gene breaks as topoisomerase II related secondary acute leukemiasG Cimino, M C Rapanotti, A Biondi, et al.
Blood|August 1, 1987
The 3' ends of the deletions of Spanish delta beta zero-thalassemia and black HPFH 1 and 2 lie within 17 kilobasesC Camaschella, A Serra, G Saglio, et al.
Haematologica|November 24, 1998
Expression of cell cycle regulatory genes in chronic myelogenous leukemiaA Iolascon, F Della Ragione, L Giordani, et al.
American Journal of Human Genetics|March 1, 1991
Screening for mutations in the phenylalanine hydroxylase gene from Italian patients with phenylketonuria by using the chemical cleavage method: a new splice mutationI Dianzani, S M Forrest, C Camaschella, et al.
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