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Matteo Doglio

Showing results (21-30 of 27) with videos related to

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Med (New York, N.Y.)|June 15, 2026
Long-term remission of neuromyelitis optica with allogeneic hematopoietic stem cell transplantGiorgio Orofino, Angela Genchi, Maria Teresa Lupo Stanghellini, et al.
Orphanet Journal of Rare Diseases|October 20, 2017
A web-based collection of genotype-phenotype associations in hereditary recurrent fevers from the Eurofever registryRiccardo Papa, Matteo Doglio, Helen J Lachmann, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|May 24, 2016
The Phenotype and Genotype of Mevalonate Kinase Deficiency: A Series of 114 Cases From the Eurofever RegistryNienke M Ter Haar, Jerold Jeyaratnam, Helen J Lachmann, et al.
Haematologica|October 6, 2022
Cytomegalovirus-specific T cells restricted for shared and donor human leukocyte antigens differentially impact on cytomegalovirus reactivation risk after allogeneic hematopoietic stem cell transplantationElena Tassi, Maddalena Noviello, Pantaleo De Simone, et al.
Science Translational Medicine|February 9, 2022
CRISPR-based gene disruption and integration of high-avidity, WT1-specific T cell receptors improve antitumor T cell functionEliana Ruggiero, Erica Carnevale, Aaron Prodeus, et al.
Frontiers in Immunology|October 17, 2022
Case Report: Consistent disease manifestations with a staggered time course in two identical twins affected by adenosine deaminase 2 deficiencyFederica Barzaghi, Maria Pia Cicalese, Matteo Zoccolillo, et al.
Science Translational Medicine|May 1, 2024
Early skeletal outcomes after hematopoietic stem and progenitor cell gene therapy for Hurler syndromeGiulia Consiglieri, Francesca Tucci, Maurizio De Pellegrin, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Med (New York, N.Y.)|June 15, 2026
Long-term remission of neuromyelitis optica with allogeneic hematopoietic stem cell transplantGiorgio Orofino, Angela Genchi, Maria Teresa Lupo Stanghellini, et al.
Orphanet Journal of Rare Diseases|October 20, 2017
A web-based collection of genotype-phenotype associations in hereditary recurrent fevers from the Eurofever registryRiccardo Papa, Matteo Doglio, Helen J Lachmann, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|May 24, 2016
The Phenotype and Genotype of Mevalonate Kinase Deficiency: A Series of 114 Cases From the Eurofever RegistryNienke M Ter Haar, Jerold Jeyaratnam, Helen J Lachmann, et al.
Haematologica|October 6, 2022
Cytomegalovirus-specific T cells restricted for shared and donor human leukocyte antigens differentially impact on cytomegalovirus reactivation risk after allogeneic hematopoietic stem cell transplantationElena Tassi, Maddalena Noviello, Pantaleo De Simone, et al.
Science Translational Medicine|February 9, 2022
CRISPR-based gene disruption and integration of high-avidity, WT1-specific T cell receptors improve antitumor T cell functionEliana Ruggiero, Erica Carnevale, Aaron Prodeus, et al.
Frontiers in Immunology|October 17, 2022
Case Report: Consistent disease manifestations with a staggered time course in two identical twins affected by adenosine deaminase 2 deficiencyFederica Barzaghi, Maria Pia Cicalese, Matteo Zoccolillo, et al.
Science Translational Medicine|May 1, 2024
Early skeletal outcomes after hematopoietic stem and progenitor cell gene therapy for Hurler syndromeGiulia Consiglieri, Francesca Tucci, Maurizio De Pellegrin, et al.
Pageof 3