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Lucia D Notarangelo

Showing results (21-30 of 33) with videos related to

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Blood Transfusion = Trasfusione Del Sangue|June 12, 2019
Physical activity improved by adherence to prophylaxis in an Italian population of children, adolescents and adults with severe haemophilia A: the SHAPE StudyEzio Zanon, Annarita Tagliaferri, Samantha Pasca, et al.
Journal of Pediatric Hematology/Oncology|January 15, 2019
Human Fibrinogen Concentrate and Fresh Frozen Plasma in the Management of Severe Acquired Hypofibrinogenemia in Children With Acute Lymphoblastic Leukemia: Results of a Retrospective SurveyPaola Giordano, Massimo Grassi, Paola Saracco, et al.
Blood|April 7, 2011
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 familiesPatrizia Noris, Silverio Perrotta, Marco Seri, et al.
British Journal of Haematology|February 27, 2015
Are all cases of paediatric essential thrombocythaemia really myeloproliferative neoplasms? Analysis of a large cohortMaria L Randi, Giulia Geranio, Irene Bertozzi, et al.
Blood Transfusion = Trasfusione Del Sangue|September 7, 2023
Recommendations for the management of acute immune thrombocytopenia in children. A Consensus Conference from the Italian Association of Pediatric Hematology and OncologyGiovanna Russo, Emilia Parodi, Piero Farruggia, et al.
Clinical Immunology (Orlando, Fla.)|February 8, 2011
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndromeCinzia Mazza, Fabio Buzi, Federica Ortolani, et al.
Scientific Reports|January 12, 2017
Alterations in the brain adenosine metabolism cause behavioral and neurological impairment in ADA-deficient mice and patientsAisha V Sauer, Raisa Jofra Hernandez, Francesca Fumagalli, et al.
The Journal of Allergy and Clinical Immunology|July 9, 2013
Whole-exome sequencing identifies tetratricopeptide repeat domain 7A (TTC7A) mutations for combined immunodeficiency with intestinal atresiasRui Chen, Silvia Giliani, Gaetana Lanzi, et al.
Msphere|December 14, 2018
Metagenomic Discovery of 83 New Human Papillomavirus Types in Patients with ImmunodeficiencyDiana V Pastrana, Alberto Peretti, Nicole L Welch, et al.
Frontiers in Medicine|April 4, 2022
Transfusional Approach in Multi-Ethnic Sickle Cell Patients: Real-World Practice Data From a Multicenter Survey in ItalyGiovanna Graziadei, Lucia De Franceschi, Laura Sainati, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Blood Transfusion = Trasfusione Del Sangue|June 12, 2019
Physical activity improved by adherence to prophylaxis in an Italian population of children, adolescents and adults with severe haemophilia A: the SHAPE StudyEzio Zanon, Annarita Tagliaferri, Samantha Pasca, et al.
Journal of Pediatric Hematology/Oncology|January 15, 2019
Human Fibrinogen Concentrate and Fresh Frozen Plasma in the Management of Severe Acquired Hypofibrinogenemia in Children With Acute Lymphoblastic Leukemia: Results of a Retrospective SurveyPaola Giordano, Massimo Grassi, Paola Saracco, et al.
Blood|April 7, 2011
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 familiesPatrizia Noris, Silverio Perrotta, Marco Seri, et al.
British Journal of Haematology|February 27, 2015
Are all cases of paediatric essential thrombocythaemia really myeloproliferative neoplasms? Analysis of a large cohortMaria L Randi, Giulia Geranio, Irene Bertozzi, et al.
Blood Transfusion = Trasfusione Del Sangue|September 7, 2023
Recommendations for the management of acute immune thrombocytopenia in children. A Consensus Conference from the Italian Association of Pediatric Hematology and OncologyGiovanna Russo, Emilia Parodi, Piero Farruggia, et al.
Clinical Immunology (Orlando, Fla.)|February 8, 2011
Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndromeCinzia Mazza, Fabio Buzi, Federica Ortolani, et al.
Scientific Reports|January 12, 2017
Alterations in the brain adenosine metabolism cause behavioral and neurological impairment in ADA-deficient mice and patientsAisha V Sauer, Raisa Jofra Hernandez, Francesca Fumagalli, et al.
The Journal of Allergy and Clinical Immunology|July 9, 2013
Whole-exome sequencing identifies tetratricopeptide repeat domain 7A (TTC7A) mutations for combined immunodeficiency with intestinal atresiasRui Chen, Silvia Giliani, Gaetana Lanzi, et al.
Msphere|December 14, 2018
Metagenomic Discovery of 83 New Human Papillomavirus Types in Patients with ImmunodeficiencyDiana V Pastrana, Alberto Peretti, Nicole L Welch, et al.
Frontiers in Medicine|April 4, 2022
Transfusional Approach in Multi-Ethnic Sickle Cell Patients: Real-World Practice Data From a Multicenter Survey in ItalyGiovanna Graziadei, Lucia De Franceschi, Laura Sainati, et al.
Pageof 4