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2019

Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects

Gorski, M. M., Lecchi, A., Femia, E. A., La Marca, S., Cairo, A., Pappalardo, E., Lotta, L. A., Artoni, A. & Peyvandi, F., Jan 1 2019, In : Haematologica. 104, 10, p. 2084-2090 7 p.

Research output: Contribution to journalArticle

Open Access

Risk of diagnostic delay in congenital thrombotic thrombocytopenic purpura

Ferrari, B., Cairo, A., Pagliari, M. T., Mancini, I., Arcudi, S. & Peyvandi, F., Apr 1 2019, In : Journal of Thrombosis and Haemostasis. 17, 4, p. 666-669 4 p.

Research output: Contribution to journalArticle

2018

Next-generation DNA sequencing to identify novel genetic risk factors for cerebral vein thrombosis

Gorski, M. M., de Haan, H. G., Mancini, I., Lotta, L. A., Bucciarelli, P., Passamonti, S. M., Cairo, A., Pappalardo, E., van Hylckama Vlieg, A., Martinelli, I., Rosendaal, F. R. & Peyvandi, F., Sep 1 2018, In : Thrombosis Research. 169, p. 76-81 6 p.

Research output: Contribution to journalArticle

2016

Immunochip analysis identifies novel susceptibility loci in the human leukocyte antigen region for acquired thrombotic thrombocytopenic purpura

Mancini, I., Ricaño-Ponce, I., Pappalardo, E., Cairo, A., Gorski, M. M., Casoli, G., Ferrari, B., Alberti, M., Mikovic, D., Noris, M., Wijmenga, C., Peyvandi, F., Rinaldi, E., Melpignano, A., Campus, S., Podda, R. A., Caria, M. C., Caddori, A., Di Francesco, E., Giuffrida, G. & 23 others, Agostini, V., Roncarati, U., Mannarella, C., Fragasso, A., Podda, G. M., Bertinato, E., Cerbone, A. M., Tufano, A., Loffredo, G., Poggi, V., Pizzuti, M., Re, G., Ronchi, M., Codeluppi, K., Facchini, L., Fanti, A., Amarri, S., Trisolini, S. M., Capria, S., Aprile, L., Defina, M., Cerù, S. & the Italian Group of TTP Investigators, Dec 1 2016, In : Journal of Thrombosis and Haemostasis. 14, 12, p. 2356-2367 12 p.

Research output: Contribution to journalArticle

Immunochip analysis identifies novel susceptibility loci in the human leukocyte antigen region for acquired thrombotic thrombocytopenic purpura

Mancini, I., Ricaño-Ponce, I., Pappalardo, E., Cairo, A., Gorski, M. M., Casoli, G., Ferrari, B., Alberti, M., Mikovic, D., Noris, M., Wijmenga, C., Peyvandi, F., Investigators, T. I. G. O. TTP., Rinaldi, E., Melpignano, A., Campus, S., Podda, R. A., Caria, M. C., Caddori, A., Di Francesco, E. & 23 others, Giuffrida, G., Agostini, V., Roncarati, U., Mannarella, C., Fragasso, A., Podda, G. M., Bertinato, E., Cerbone, A. M., Tufano, A., Loffredo, G., Poggi, V., Pizzuti, M., Re, G., Ronchi, M., Codeluppi, K., Facchini, L., Fanti, A., Amarri, S., Trisolini, S. M., Capria, S., Aprile, L., Defina, M. & Cerù, S., 2016, In : Journal of Thrombosis and Haemostasis. 14, 12, p. 2356-2367 12 p.

Research output: Contribution to journalArticle

The D173G mutation in ADAMTS-13 causes a severe form of congenital thrombotic thrombocytopenic purpura: A clinical, biochemical and in silico study

Lancellotti, S., Peyvandi, F., Pagliari, M. T., Cairo, A., Abdel-Azeim, S., Chermak, E., Lazzareschi, I., Mastrangelo, S., Cavallo, L., Oliva, R. & De Cristofaro, R., 2016, In : Thrombosis and Haemostasis. 115, 1, p. 51-62 12 p.

Research output: Contribution to journalArticle

2015

Congenital and acquired ADAMTS13 deficiency: Two mechanisms, one patient

Ferrari, B., Cairo, A., Pontiggia, S., Mancini, I., Masini, L. & Peyvandi, F., Aug 1 2015, In : Journal of Clinical Apheresis. 30, 4, p. 252-256 5 p.

Research output: Contribution to journalArticle

Frequency of the p.Gly262Asp mutation in congenital Factor X deficiency

Epcacan, S., Menegatti, M., Akbayram, S., Cairo, A., Peyvandi, F. & Oner, A. F., Oct 1 2015, In : European Journal of Clinical Investigation. 45, 10, p. 1087-1091 5 p.

Research output: Contribution to journalArticle

Neonatal onset of congenital factor X deficiency: A description of two novel mutations with 6-year follow-up

Corsini, I., Menegatti, M., Cairo, A. & Dani, C., Sep 1 2015, In : Blood Coagulation and Fibrinolysis. 26, 6, p. 679-681 3 p.

Research output: Contribution to journalArticle

2014

Congenital factor XIII deficiency in Pakistan: Characterization of seven families and identification of four novel mutations

Borhany, M., Handrkova, H., Cairo, A., Schroeder, V., Fatima, N., Naz, A., Amanat, S., Shamsi, T., Peyvandi, F. & Kohler, H. P., 2014, In : Haemophilia. 20, 4, p. 568-574 7 p.

Research output: Contribution to journalArticle

Congenital thrombotic thrombocytopenic purpura with novel mutations in three unrelated turkish children

Metin, A., Unal, S., Gümrük, F., Palla, R., Cairo, A., Underwood, M. & Gurgey, A., Mar 2014, In : Pediatric Blood and Cancer. 61, 3, p. 558-561 4 p.

Research output: Contribution to journalArticle

Genotype and phenotype report on patients with combined deficiency of factor v and factor VIII in Iran

Karimi, M., Cairo, A., Safarpour, M. M., Haghpanah, S., Ekramzadeh, M., Afrasiabi, A., Shahriari, M. & Menegatti, M., 2014, In : Blood Coagulation and Fibrinolysis. 25, 4, p. 360-363 4 p.

Research output: Contribution to journalArticle

Spontaneous epidural hematoma in a child with inherited factor XIII deficiency

Farah, R. A., Al Danaf, J. Z., Chahinian, R. A., Braiteh, N. T., Al Ojaimi, N. F., Cairo, A., Farhat, H. & Mantoura, J. R., Jan 2014, In : Journal of Pediatric Hematology/Oncology. 36, 1, p. 62-65 4 p.

Research output: Contribution to journalArticle

Two novel heterozygote missense mutations of the ADAMTS13 gene in a child with recurrent Thrombotic thrombocytopenic purpura

Rossio, R., Ferrari, B., Cairo, A., Mancini, I., Pisapia, G., Palazzo, G. & Peyvandi, F., 2013, In : Blood Transfusion. 11, 2, p. 241-244 4 p.

Research output: Contribution to journalArticle

2011

B and T lymphocytes in acquired Thrombotic Thrombocytopenic Purpura during disease remission

Mariani, M., Cairo, A., Palla, R., Lotta, L. A., Consonni, D., Rovati, A., Trisolini, S. & Peyvandi, F., Dec 2011, In : Thrombosis Research. 128, 6, p. 590-592 3 p.

Research output: Contribution to journalArticle

Novel aspects of factor XIII deficiency

Muszbek, L., Bagoly, Z., Cairo, A. & Peyvandi, F., Sep 2011, In : Current Opinion in Hematology. 18, 5, p. 366-372 7 p.

Research output: Contribution to journalArticle

2010

ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura

Lotta, L. A., Garagiola, I., Palla, R., Cairo, A. & Peyvandi, F., Jan 2010, In : Human Mutation. 31, 1, p. 11-19 9 p.

Research output: Contribution to journalArticle

2006

The thrombospondin-1 N700S polymorphism is associated with early myocardial infarction without altering von Willebrand factor multimer size

Zwicker, J. I., Peyvandi, F., Palla, R., Lombardi, R., Canciani, M. T., Cairo, A., Ardissino, D., Bernardinelli, L., Bauer, K. A., Lawler, J. & Mannucci, P., Aug 15 2006, In : Blood. 108, 4, p. 1280-1283 4 p.

Research output: Contribution to journalArticle