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Journal Articles

An Alternatively Spliced Form of CD79b Gene May Account for Altered B-Cell Receptor Expression in B-Chronic Lymphocytic Leukemia

A. Alfarano, S. Indraccolo, P. Circosta, S. Minuzzo, A. Vallario, R. Zamarchi, A. Fregonese, F. Calderazzo, A. Faldella, M. Aragno, C. Camaschella, A. Amadori, F. Caligaris-Cappio

Blood (1999) 93 (7): 2327–2335.

https://doi.org/10.1182/blood.V93.7.2327

Published: 1999

Journal Articles

Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemia

P Fortina, T Parrella, M Sartore, E Gottardi, V Gabutti, K Delgrosso, E Mansfield, E Rappaport, E Schwartz, C Camaschella

Blood (1994) 83 (11): 3356–3362.

https://doi.org/10.1182/blood.V83.11.3356.3356

Published: 1994

Journal Articles

Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutations

S Murru, G Loudianos, M Deiana, C Camaschella, GV Sciarratta, S Agosti, MI Parodi, P Cerruti, A Cao, M Pirastu

Blood (1991) 77 (6): 1342–1347.

https://doi.org/10.1182/blood.V77.6.1342.1342

Published: 1991

Journal Articles

Molecular characterization of hereditary persistence of fetal hemoglobin in a patient from Cuba [letter]

G Martinez, A Hernandez, L Corral, A Muniz, C Alaez, A Serra, A Alfarano, G Saglio, C Camaschella

Blood (1990) 76 (6): 1262–1263.

https://doi.org/10.1182/blood.V76.6.1262.1262

Published: 1990

Journal Articles

Prenatal diagnosis of fetal hemoglobin Lepore-Boston disease on maternal peripheral blood

C Camaschella, A Alfarano, E Gottardi, M Travi, P Primignani, F Caligaris Cappio, G Saglio

Blood (1990) 75 (11): 2102–2106.

https://doi.org/10.1182/blood.V75.11.2102.2102

Published: 1990

Journal Articles

A new hereditary persistence of fetal hemoglobin deletion has the breakpoint within the 3' beta-globin gene enhancer

C Camaschella, A Serra, E Gottardi, A Alfarano, D Revello, U Mazza, G Saglio

Blood (1990) 75 (4): 1000–1005.

https://doi.org/10.1182/blood.V75.4.1000.1000

Published: 1990

Journal Articles

The homozygous state of G to A--117A gamma hereditary persistence of fetal hemoglobin

C Camaschella, L Oggiano, M Sampietro, E Gottardi, A Alfarano, P Pistidda, F Dore, R Taramelli, S Ottolenghi, M Longinotti

Blood (1989) 73 (7): 1999–2002.

https://doi.org/10.1182/blood.V73.7.1999.1999

Published: 1989

Journal Articles

Delineation of specific beta-thalassemia mutations in high-risk areas of Italy: a prerequisite for prenatal diagnosis

M Pirastu, G Saglio, C Camaschella, A Loi, A Serra, T Bertero, W Gabutti, A Cao

Blood (1988) 71 (4): 983–988.

https://doi.org/10.1182/blood.V71.4.983.983

Published: 1988

Journal Articles

The 3' ends of the deletions of Spanish delta beta zero-thalassemia and black HPFH 1 and 2 lie within 17 kilobases

C Camaschella, A Serra, G Saglio, M Baiget, N Malgaretti, R Mantovani, S Ottolenghi

Blood (1987) 70 (2): 593–596.

https://doi.org/10.1182/blood.V70.2.593.593

Published: 1987

Journal Articles

Sardinian delta beta zero-thalassemia: a further example of a C to T substitution at position -196 of the A gamma globin gene promoter

S Ottolenghi, B Giglioni, A Pulazzini, P Comi, C Camaschella, A Serra, A Guerrasio, G Saglio

Blood (1987) 69 (4): 1058–1061.

https://doi.org/10.1182/blood.V69.4.1058.1058

Published: 1987

Journal Articles

Italian type of deletional hereditary persistence of fetal hemoglobin

G Saglio, C Camaschella, A Serra, T Bertero, G Rege Cambrin, A Guerrasio, U Mazza, P Izzo, F Terragni, B Giglioni

Blood (1986) 68 (3): 646–651.

https://doi.org/10.1182/blood.V68.3.646.646

Published: 1986

Journal Articles

Interaction between Hb Hasharon and alpha-thalassemia: an approach to the problem of the number of human alpha loci

P Pich, G Saglio, C Camaschella, O David, MA Vasino, G Ricco, U Mazza

Blood (1978) 51 (2): 339–346.

https://doi.org/10.1182/blood.V51.2.339.339

Published: 1978

Journal Articles

The relationship between anemia, fecal stercobilinogen, erythrocyte survival, and globin synthesis in heterozygotes for beta-thalassemia

E Gallo, P Pich, G Ricco, G Saglio, C Camaschella, U Mazza

Blood (1975) 46 (5): 693–698.

https://doi.org/10.1182/blood.V46.5.693.693

Published: 1975

NARROW

An Alternatively Spliced Form of CD79b Gene May Account for Altered B-Cell Receptor Expression in B-Chronic Lymphocytic Leukemia

Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemia

Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutations

Molecular characterization of hereditary persistence of fetal hemoglobin in a patient from Cuba [letter]

Prenatal diagnosis of fetal hemoglobin Lepore-Boston disease on maternal peripheral blood

A new hereditary persistence of fetal hemoglobin deletion has the breakpoint within the 3' beta-globin gene enhancer

The homozygous state of G to A--117A gamma hereditary persistence of fetal hemoglobin

Delineation of specific beta-thalassemia mutations in high-risk areas of Italy: a prerequisite for prenatal diagnosis

The 3' ends of the deletions of Spanish delta beta zero-thalassemia and black HPFH 1 and 2 lie within 17 kilobases

Sardinian delta beta zero-thalassemia: a further example of a C to T substitution at position -196 of the A gamma globin gene promoter

Italian type of deletional hereditary persistence of fetal hemoglobin

Interaction between Hb Hasharon and alpha-thalassemia: an approach to the problem of the number of human alpha loci

The relationship between anemia, fecal stercobilinogen, erythrocyte survival, and globin synthesis in heterozygotes for beta-thalassemia

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American Society of Hematology

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American Society of Hematology

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