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Simona Ferrari

Showing results (41-50 of 73) with videos related to

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European Journal of Pediatrics|October 1, 2018
Follow-up and outcome of symptomatic partial or absolute IgA deficiency in childrenViviana Moschese, Loredana Chini, Simona Graziani, et al.
Frontiers in Immunology|May 19, 2023
Case Report: Interindividual variability and possible role of heterozygous variants in a family with deficiency of adenosine deaminase 2: are all heterozygous born equals?Federica Pulvirenti, Bianca Laura Cinicola, Simona Ferrari, et al.
BMJ Health & Care Informatics|December 31, 2025
Machine learning prediction of germline <i>BRCA1/2</i> pathogenic variants in patients with ovarian cancerGiovanni Innella, Giulia Erini, Antonio De Leo, et al.
Epilepsia|March 4, 2014
Autosomal dominant partial epilepsy with auditory features: a new locus on chromosome 19q13.11-q13.31Francesca Bisulli, Ilaria Naldi, Sara Baldassari, et al.
Frontiers in Immunology|October 23, 2023
Decline of gastric cancer mortality in common variable immunodeficiency in the years 2018-2022Cinzia Milito, Federica Pulvirenti, Giulia Garzi, et al.
Haematologica|August 2, 2007
Congenital amegakaryocytic thrombocytopenia: clinical and biological consequences of five novel mutationsAnna Savoia, Carlo Dufour, Franco Locatelli, et al.
Molecular Cytogenetics|August 4, 2015
Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degenerationPamela Magini, Monica Poscente, Simona Ferrari, et al.
International Journal of Molecular Sciences|September 27, 2025
Neuroinflammation in CTLA-4 Haploinsufficiency: Case Report of a New Variant with Remarkable Response to Targeted TherapyLetizia Baldini, Lucia Del Vecchio, Sara Cerasi, et al.
Cells|June 24, 2022
T-Cell Defects Associated to Lack of Spike-Specific Antibodies after BNT162b2 Full Immunization Followed by a Booster Dose in Patients with Common Variable Immune DeficienciesFederica Pulvirenti, Stefano Di Cecca, Matilde Sinibaldi, et al.
International Journal of Molecular Sciences|June 2, 2021
Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next?Roberta Zuntini, Elena Bonora, Laura Maria Pradella, et al.
Pageof 8

Showing results (41-50 of 73) with videos related to

Sort By:
Pageof 8
European Journal of Pediatrics|October 1, 2018
Follow-up and outcome of symptomatic partial or absolute IgA deficiency in childrenViviana Moschese, Loredana Chini, Simona Graziani, et al.
Frontiers in Immunology|May 19, 2023
Case Report: Interindividual variability and possible role of heterozygous variants in a family with deficiency of adenosine deaminase 2: are all heterozygous born equals?Federica Pulvirenti, Bianca Laura Cinicola, Simona Ferrari, et al.
BMJ Health & Care Informatics|December 31, 2025
Machine learning prediction of germline <i>BRCA1/2</i> pathogenic variants in patients with ovarian cancerGiovanni Innella, Giulia Erini, Antonio De Leo, et al.
Epilepsia|March 4, 2014
Autosomal dominant partial epilepsy with auditory features: a new locus on chromosome 19q13.11-q13.31Francesca Bisulli, Ilaria Naldi, Sara Baldassari, et al.
Frontiers in Immunology|October 23, 2023
Decline of gastric cancer mortality in common variable immunodeficiency in the years 2018-2022Cinzia Milito, Federica Pulvirenti, Giulia Garzi, et al.
Haematologica|August 2, 2007
Congenital amegakaryocytic thrombocytopenia: clinical and biological consequences of five novel mutationsAnna Savoia, Carlo Dufour, Franco Locatelli, et al.
Molecular Cytogenetics|August 4, 2015
Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degenerationPamela Magini, Monica Poscente, Simona Ferrari, et al.
International Journal of Molecular Sciences|September 27, 2025
Neuroinflammation in CTLA-4 Haploinsufficiency: Case Report of a New Variant with Remarkable Response to Targeted TherapyLetizia Baldini, Lucia Del Vecchio, Sara Cerasi, et al.
Cells|June 24, 2022
T-Cell Defects Associated to Lack of Spike-Specific Antibodies after BNT162b2 Full Immunization Followed by a Booster Dose in Patients with Common Variable Immune DeficienciesFederica Pulvirenti, Stefano Di Cecca, Matilde Sinibaldi, et al.
International Journal of Molecular Sciences|June 2, 2021
Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next?Roberta Zuntini, Elena Bonora, Laura Maria Pradella, et al.
Pageof 8