Sfoglia per Autore
Clinical and biochemical study of thalassemia intermedia in Campania (southern Italy)
1987 Iolascon, A; Pinto, L; Nobili, Bruno; Lania, A; Iafusco, Dario; MIRAGLIA DEL GIUDICE, Emanuele; Matarese, Sm; Salvati, P; Cutillo, S.
A modification of the 'pink test' may improve the diagnosis of hereditary spherocytosis
1989 Pinto, L; Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Nobili, Bruno
La mineralometria ossea computerizzata nelle anemie emolitiche croniche
1990 Iolascon, Giovanni; Ronca, Dante; Pinto, L; Nobile, B; Matarese, S. M. R.; MIRAGLIA DEL GIUDICE, Emanuele; Iolascon, A.
Analysis of N-ras gene mutations in medulloblastomas by polymerase chain reaction and oligonucleotide probes in formalin-fixed, paraffin-embedded tissues
1991 Iolascon, A; Lania, A; Badiali, M; Pession, A; Saglio, G; Giangaspero, F; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Cutillo, S.
Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases
1991 Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Camaschella, C; Pinto, L; Nobili, Bruno; Perrotta, Silverio; Cutillo, S.
Hereditary spherocytosis characterized by increased spectrin/band 3 ratio
1992 MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Pinto, L; Cappellini, Md; Fiorelli, G; Cutillo, S; Iolascon, A.
Alpha I/65 hereditary elliptocytosis in southern Italy: evidence for an African origin
1992 MIRAGLIA DEL GIUDICE, Emanuele; Ducluzeau, Mt; Alloisio, N; Wilmotte, R; Delaunay, J; Perrotta, Silverio; Cutillo, S; Iolascon, A.
Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis
1992 Cutillo, S; Pinto, L; Nobili, Bruno; MIRAGLIA DEL GIUDICE, Emanuele; Iolascon, A.
Molecular pathology of inherited erythrocyte membrane disorders: hereditary spherocytosis and elliptocytosis
1992 Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Camaschella, C.
Hereditary spherocytosis (HS) due to loss of anion exchange transporter
1992 Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Pinto, L; Fiorelli, G; Cappellini, Dm; Vasseur, C; Bursaux, E; Cutillo, S.
Spectrin cagliari. an Ala-->Gly substitution in helix 1 of beta spectrin repeat 17 that severely disrupts the structure and self-association of the erythrocyte spectrin heterodimer
1993 Sahr, Ke; Coetzer, Tl; Moy, Ls; Derick, Lh; Chishti, Ah; Jarolim, P; Lorenzo, F; MIRAGLIA DEL GIUDICE, Emanuele; Iolascon, A; Gallanello, R.
Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotype
1993 MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Nobili, Bruno; Pinto, L; Cutillo, L; Iolascon, A.
Severe poikilocytosis associated with a de novo alpha 28 Arg-->Cys mutation in spectrin
1993 Lorenzo, F; MIRAGLIA DEL GIUDICE, Emanuele; Alloisio, N; Morle, L; Forissier, A; Perrotta, Silverio; Sciarratta, G; Iolascon, A; Delaunay, J.
A rapid method for the detection of alpha I/65 hereditary elliptocytosis
1993 Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Pinto, L; Cutillo, S.
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis
1994 MIRAGLIA DEL GIUDICE, Emanuele; Iolascon, A; Pinto, L; Nobili, Bruno; Perrotta, Silverio
A deletional frameshift mutation in spectrin beta-gene associated with hereditary elliptocytosis in spectrin Napoli
1994 Wilmotte, R; MIRAGLIA DEL GIUDICE, Emanuele; Marechal, J; Perrotta, Silverio; DE MATTIA, D; Delaunay, J; Iolascon, A.
Glucose 6-phosphate dehydrogenase deficiency and red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemia
1994 Alfinito, F; Calabro, V; Cappellini, Md; Fiorelli, G; Filosa, S; Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Migliorati, R; Vallone, D.
Molecular heterogeneity of hereditary elliptocytosis in Italy
1994 MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Sannino, E; DE ANGELIS, F; Nobili, Bruno; Iolascon, A.
Mild elliptocytosis associated with the alpha 34 Arg-->Trp mutation in spectrin Genova (alpha I/74)
1994 Perrotta, Silverio; MIRAGLIA DEL GIUDICE, Emanuele; Alloisio, N; Sciarratta, G; Pinto, L; Delaunay, J; Cutillo, S; Iolascon, A.
Increased Membrane‐Protein Methylation in Hereditary Spherocytosis: A Marker of Cytoskeletal Disarray
1995 Ingrosso, Diego; D'Angelo, S.; Perna, Alessandra; Iolascon, A.; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Zappia, V.; Galletti, P.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Clinical and biochemical study of thalassemia intermedia in Campania (southern Italy) | 1-gen-1987 | Iolascon, A; Pinto, L; Nobili, Bruno; Lania, A; Iafusco, Dario; MIRAGLIA DEL GIUDICE, Emanuele; Matarese, Sm; Salvati, P; Cutillo, S. | |
A modification of the 'pink test' may improve the diagnosis of hereditary spherocytosis | 1-gen-1989 | Pinto, L; Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Nobili, Bruno | |
La mineralometria ossea computerizzata nelle anemie emolitiche croniche | 1-gen-1990 | Iolascon, Giovanni; Ronca, Dante; Pinto, L; Nobile, B; Matarese, S. M. R.; MIRAGLIA DEL GIUDICE, Emanuele; Iolascon, A. | |
Analysis of N-ras gene mutations in medulloblastomas by polymerase chain reaction and oligonucleotide probes in formalin-fixed, paraffin-embedded tissues | 1-gen-1991 | Iolascon, A; Lania, A; Badiali, M; Pession, A; Saglio, G; Giangaspero, F; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Cutillo, S. | |
Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases | 1-gen-1991 | Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Camaschella, C; Pinto, L; Nobili, Bruno; Perrotta, Silverio; Cutillo, S. | |
Hereditary spherocytosis characterized by increased spectrin/band 3 ratio | 1-gen-1992 | MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Pinto, L; Cappellini, Md; Fiorelli, G; Cutillo, S; Iolascon, A. | |
Alpha I/65 hereditary elliptocytosis in southern Italy: evidence for an African origin | 1-gen-1992 | MIRAGLIA DEL GIUDICE, Emanuele; Ducluzeau, Mt; Alloisio, N; Wilmotte, R; Delaunay, J; Perrotta, Silverio; Cutillo, S; Iolascon, A. | |
Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis | 1-gen-1992 | Cutillo, S; Pinto, L; Nobili, Bruno; MIRAGLIA DEL GIUDICE, Emanuele; Iolascon, A. | |
Molecular pathology of inherited erythrocyte membrane disorders: hereditary spherocytosis and elliptocytosis | 1-gen-1992 | Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Camaschella, C. | |
Hereditary spherocytosis (HS) due to loss of anion exchange transporter | 1-gen-1992 | Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Pinto, L; Fiorelli, G; Cappellini, Dm; Vasseur, C; Bursaux, E; Cutillo, S. | |
Spectrin cagliari. an Ala-->Gly substitution in helix 1 of beta spectrin repeat 17 that severely disrupts the structure and self-association of the erythrocyte spectrin heterodimer | 1-gen-1993 | Sahr, Ke; Coetzer, Tl; Moy, Ls; Derick, Lh; Chishti, Ah; Jarolim, P; Lorenzo, F; MIRAGLIA DEL GIUDICE, Emanuele; Iolascon, A; Gallanello, R. | |
Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotype | 1-gen-1993 | MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Nobili, Bruno; Pinto, L; Cutillo, L; Iolascon, A. | |
Severe poikilocytosis associated with a de novo alpha 28 Arg-->Cys mutation in spectrin | 1-gen-1993 | Lorenzo, F; MIRAGLIA DEL GIUDICE, Emanuele; Alloisio, N; Morle, L; Forissier, A; Perrotta, Silverio; Sciarratta, G; Iolascon, A; Delaunay, J. | |
A rapid method for the detection of alpha I/65 hereditary elliptocytosis | 1-gen-1993 | Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Pinto, L; Cutillo, S. | |
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis | 1-gen-1994 | MIRAGLIA DEL GIUDICE, Emanuele; Iolascon, A; Pinto, L; Nobili, Bruno; Perrotta, Silverio | |
A deletional frameshift mutation in spectrin beta-gene associated with hereditary elliptocytosis in spectrin Napoli | 1-gen-1994 | Wilmotte, R; MIRAGLIA DEL GIUDICE, Emanuele; Marechal, J; Perrotta, Silverio; DE MATTIA, D; Delaunay, J; Iolascon, A. | |
Glucose 6-phosphate dehydrogenase deficiency and red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemia | 1-gen-1994 | Alfinito, F; Calabro, V; Cappellini, Md; Fiorelli, G; Filosa, S; Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Migliorati, R; Vallone, D. | |
Molecular heterogeneity of hereditary elliptocytosis in Italy | 1-gen-1994 | MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Sannino, E; DE ANGELIS, F; Nobili, Bruno; Iolascon, A. | |
Mild elliptocytosis associated with the alpha 34 Arg-->Trp mutation in spectrin Genova (alpha I/74) | 1-gen-1994 | Perrotta, Silverio; MIRAGLIA DEL GIUDICE, Emanuele; Alloisio, N; Sciarratta, G; Pinto, L; Delaunay, J; Cutillo, S; Iolascon, A. | |
Increased Membrane‐Protein Methylation in Hereditary Spherocytosis: A Marker of Cytoskeletal Disarray | 1-gen-1995 | Ingrosso, Diego; D'Angelo, S.; Perna, Alessandra; Iolascon, A.; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Zappia, V.; Galletti, P. |
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