GUISO, LUCIA ANNA

GUISO, LUCIA ANNA  

Istituto di Ricerca Genetica e Biomedica - IRGB - Sede Secondaria Sassari  

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Titolo Data di pubblicazione Autore(i) File
The homozygous state of Hb J Sardegna 1-gen-2002 Pistidda P.; Guiso L.; Frogheri L.; Longinotti M.
Expression of bcl-2 Genes Family in Circulating Erythroblasts of Patients with Thalassemia Intermedia 1-gen-2001 Frogheri, L; Maddau, G; Guiso, L; Pistidda, P; Bonfigli, S; Longinotti, M; Dore, F
Membrane Phospholipids Asymmetry In Circulating Erythroblasts Of Patients With beta-Thalassemia Intermedia 1-gen-1999 Frogheri L.; Dore F.; Bonfigli S.; Guiso L.; Maddau G.; Pistidda P.; Longinotti M.
bcl-x Expression In Circulating Erythroblasts From Patients With Ineffective Erythropoiesis 1-gen-1998 Frogheri L.; Dore F.; Bonfigli S.; Pistidda P.; Guiso L.; Longinotti M.
Maximal gamma-globin expression in the compound heterozygous state for -175(G)gamma HPFH and beta degrees 39 nonsense thalassaemia: A case study 1-gen-1997 Pistidda, P; Frogheri, L; Guiso, L; Manca, L; Dore, F; Mura, L; Longinotti, M
Fetal hemoglobin expression in the compound heterozygous state for nondeletional HPFH and beta-thalassemia 1-gen-1996 Frogheri, L; Pistidda, P; Guiso, L; Dore, F; Mura, L; Longinotti, M
Frequency and phenotype of delta+-thalassemia in Sardinia 1-gen-1996 Guiso L.; Frogheri L.; Pistidda P.; Angioni L.; Bonfigli S.; Longinotti M.; Dore F
Frequency of delta(+)27-thalassaemia in Sardinians 1-gen-1996 Guiso, L; Frogheri, L; Pistidda, P; Angioni, L; Dore, F; Pardini, S; Longinotti, M
Wide-scale re-evaluation of the incidence of beta-thalassemia in Sardinia 1-gen-1996 Longinotti, M; Dore, F; Pardini, S; Pistidda, P; Guiso, L; Frogheri, L; Bonfigli, S; Nieddu, R M; Oggiano, L; Inzaina, A; Mulas, P
FETAL HEMOGLOBIN EXPRESSION IN COMPOUND HETEROZYGOTES FOR -117(G-]A) (A)GAMMA HPFH AND BETA(O)39 NONSENSE THALASSEMIA 1-gen-1995 PISTIDDA, P; FROGHERI, L; OGGIANO, L; GUISO, L; MANCA, L; DORE, F; MASALA, B; GILMAN, JG; LONGINOTTI, M
A NOVEL MEDITERRANEAN DELTA-BETA-THALASSEMIA DETERMINANT CONTAINING THE DELTA+27 AND BETA-DEGREES-39 POINT MUTATIONS IN CIS 1-gen-1994 Oggiano, L; Guiso, L; Frogheri, L; Loudianos, G; Pistidda, P; Rimini, E; Pirastu, M; Cao, A; Longinotti, M
MILD BETA+(-87)-THALASSEMIA CACCC BOX MUTATION IS ASSOCIATED WITH ELEVATED FETAL HEMOGLOBIN EXPRESSION IN CIS 1-gen-1994 Gilman, Jg; Manca, L; Frogheri, L; Pistidda, P; Guiso, L; Longinotti, M; Masala, B
Differential diagnosis in thalassemia syndromes|DIAGNOSI DIFFERENZIALE DELLE SINDROMI TALASSEMICHE 1-gen-1992 Dore, F; Pardini, S; Bonfigli, S; Oggiano, L; Murineddu, M; Pistidda, P; Guiso, L; Frogheri, L; Gaviano, E; Longinotti, M
HEMATOLOGICAL PHENOTYPES IN A FAMILY WITH TRIPLICATED ALPHA-GLOBIN GENE, BETA(39) AND DELTA+(27) THALASSEMIA MUTATIONS 1-gen-1992 OGGIANO, L; RIMINI, E; FROGHERI, L; GUISO, L; PISTIDDA, P; LONGINOTTI, M
THALASSEMIA INTERMEDIA TODAY 1-gen-1992 LONGINOTTI M; DORE F; OGGIANO L; PARDINI S; PISTIDDA P; GUISO L; FROGHERI L; BONFIGLI S; MURINEDDU M; RIMINI E