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Your search keyword '"Cerri, R."' showing total 6 results
Start Over Author "Cerri, R." Journal acta haematologica
6 results on '"Cerri, R."'

1. Bone Marrow Transplantation for Severe Aplastic Anemia.

Author

Marmont, A.M., Van Lint, M.T., Avanzi, G., Reali, G., Adami, R., Soldá, A., Strada, P., Barbanti, M., Mingari, M.C., Soro, O., Grazi, G., Pedullá, D., Cerri, R., Rossi, E., Giordano, D., Santini, G., Carella, A., Risso, M., Vimercati, R., and Piaggio, G.

Published
1979
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3. Bone Marrow Transplantation for Severe Aplastic Anemia

Author

D. Pedulla, Almalina Bacigalupo, E. Librace, Edoardo Rossi, Angelo Michele Carella, G. Reali, D. Giordano, R. Vimercati, Maria Cristina Mingari, Alberto M. Marmont, Gino Santini, A. Solda, M. R. Raffo, O. Soro, Cerri R, M. Barbanti, M. T. Van Lint, Paolo Strada, G. Grazi, G. Avanzi, V. Vitale, R. Adami, Giovanna Piaggio, and Marco Risso

Subjects
medicine.medical_specialty, Bone marrow transplantation, Cyclophosphamide, business.industry, Hematology, General Medicine, medicine.disease, Severe Aplastic Anemia, Gastroenterology, surgical procedures, operative, hemic and lymphatic diseases, Internal medicine, Medicine, Aplastic anemia, business, medicine.drug
Abstract

9 patients with severe aplastic anemia (SAA) were treated with bone marrow transplantation (BMT). 5 were conditioned with cyclophosphamide and received and HLA-identical graft (4 patients) or a mismat

Published
1979
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4. A New Chromosome Translocation (3;21) in M2 Acute Lymphocytic Leukemia

Author

C. Rabitti, C. Parodi, Marco Risso, Cerri R, S. De Filippi, Almalina Bacigalupo, A. Castellaneta, A. M. Marmont, and A. Caimo

Subjects
Genetics, medicine.medical_specialty, Adolescent, Chromosomes, Human, 1-3, Cytogenetics, Chromosomal translocation, Karyotype, Hematology, General Medicine, Biology, medicine.disease, Molecular biology, Translocation, Genetic, Chromosome Banding, Leukemia, Lymphoid, Leukemia, Chromosome 3, Karyotyping, hemic and lymphatic diseases, Acute lymphocytic leukemia, Chromosomes, Human, 21-22 and Y, medicine, Humans, Female, Chromosome 21
Abstract

High-resolution chromosome banding studies were carried out on leukemic cells from a young patient with acute nonlymphocytic leukemia (ANLL), M2 of the FAB classification. A new chromosomal abnormality involving a translocation between chromosomes 3 and 21 was observed, i.e., t(3;21)(p14;q22). A complete remission was never obtained in spite of aggressive chemotherapy and the patient died 8 months after diagnosis.

Published
1986
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5. Positive direct antiglobulin tests and heteroimmune hemolysis in patients with severe aplastic anemia and pure red cell anemia treated with antilymphocytic globulin

Author

Cerri R, A. M. Marmont, G. Lercari, M. T. Van Lint, Marco Risso, and Almalina Bacigalupo

Subjects
congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Globulin, Pure red cell aplasia, macromolecular substances, Red-Cell Aplasia, Pure, Gastroenterology, Polymyositis, Hemolysis, Coombs test, hemic and lymphatic diseases, Internal medicine, medicine, Animals, Humans, Horses, Aplastic anemia, Congenital hypoplastic anemia, Antilymphocyte Serum, Clinical Trials as Topic, medicine.diagnostic_test, biology, business.industry, Anemia, Aplastic, Hematology, General Medicine, medicine.disease, Severe Aplastic Anemia, body regions, stomatognathic diseases, Coombs Test, biology.protein, business
Abstract

Forty-six patients with severe aplastic anemia (SAA), 1 with adult pure red cell aplasia (PRCA), 1 with congenital hypoplastic anemia (Diamond-Blackfan) and 1 with severe polymyositis were treated with intravenous antilymphocyte globulins (ALG) of different sources (2 of equine and 1 of rabbit origin). In all patients, direct and indirect antiglobulin tests (DAT and IAT) were performed, and in all patients treated with one type of equine ALG, positive DATs were found in Rh0(D)-positive patients, while the serum of Rh0(D)-negative patients treated with the same ALG reacted in vitro with Rh0(D)-positive erythrocytes. The antibody was eluted and shown to be of equine origin. Two patients suffered from frank heteroimmune hemolytic anemia. Since October 1984, the ALG of this particular source has not displayed any overt anti-erythrocyte activity any more. However, all clinicians treating patients with this type of immune immunosuppression should know that ALG may retain human erythrocyte (presumably anti-LW) activity.

Published
1985

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