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Bianca Tesi

Showing results (31-40 of 67) with videos related to

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Frontiers in Immunology|January 25, 2014
An N-Terminal Missense Mutation in STX11 Causative of FHL4 Abrogates Syntaxin-11 Binding to Munc18-2Martha-Lena Müller, Samuel C C Chiang, Marie Meeths, et al.
British Journal of Haematology|July 14, 2018
Microdeletion of 7p12.1p13, including IKZF1, causes intellectual impairment, overgrowth, and susceptibility to leukaemiaTekla Järviaho, Vasilios Zachariadis, Bianca Tesi, et al.
Journal of Pediatric Hematology/Oncology|July 11, 2017
A Case of Familial Hemophagocytic Lymphohistiocytosis Type 4 With Involvement of the Central Nervous System Complicated With InfarctSaliha Ciraci, Alper Ozcan, Mustafa M Ozdemir, et al.
Hemasphere|August 14, 2024
How to manage patients with germline <i>DDX41</i> variants: Recommendations from the Nordic working group on germline predisposition for myeloid neoplasmsPanagiotis Baliakas, Bianca Tesi, Jörg Cammenga, et al.
British Journal of Haematology|November 25, 2025
Comorbidities and mutations including single- and multihit TET2 mutations in relation to outcome in chronic myelomonocytic leukaemia-A population-based studyMatilda Kjellander Kynning, Ebba Westerberg, Linda Forsell, et al.
Pediatric Blood & Cancer|July 18, 2015
Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense MutationsBianca Tesi, Samuel C C Chiang, Dalia El-Ghoneimy, et al.
Annals of Internal Medicine|January 20, 2025
Germline <i>UBA1</i> Variant With Somatic Amplification in a Woman With Inflammatory Diseases and Myelodysplastic SyndromeMaria Creignou, Maria Sirenko, Pedro L Moura, et al.
Archivum Immunologiae Et Therapiae Experimentalis|October 22, 2021
Molecular Genetics Diversity of Primary Hemophagocytic Lymphohistiocytosis among Polish Pediatric PatientsKatarzyna Bąbol-Pokora, Magdalena Wołowiec, Katarzyna Popko, et al.
Immunity|March 19, 2015
Cytomegalovirus infection drives adaptive epigenetic diversification of NK cells with altered signaling and effector functionHeinrich Schlums, Frank Cichocki, Bianca Tesi, et al.
Frontiers in Medicine|August 14, 2023
Register-based and genetic studies of Prader-Willi syndrome show a high frequency of gonadal tumors and a possible mechanism for tumorigenesis through imprinting relaxationCarolina Maya-González, Sandra Wessman, Kristina Lagerstedt-Robinson, et al.
Pageof 7

Showing results (31-40 of 67) with videos related to

Sort By:
Pageof 7
Frontiers in Immunology|January 25, 2014
An N-Terminal Missense Mutation in STX11 Causative of FHL4 Abrogates Syntaxin-11 Binding to Munc18-2Martha-Lena Müller, Samuel C C Chiang, Marie Meeths, et al.
British Journal of Haematology|July 14, 2018
Microdeletion of 7p12.1p13, including IKZF1, causes intellectual impairment, overgrowth, and susceptibility to leukaemiaTekla Järviaho, Vasilios Zachariadis, Bianca Tesi, et al.
Journal of Pediatric Hematology/Oncology|July 11, 2017
A Case of Familial Hemophagocytic Lymphohistiocytosis Type 4 With Involvement of the Central Nervous System Complicated With InfarctSaliha Ciraci, Alper Ozcan, Mustafa M Ozdemir, et al.
Hemasphere|August 14, 2024
How to manage patients with germline <i>DDX41</i> variants: Recommendations from the Nordic working group on germline predisposition for myeloid neoplasmsPanagiotis Baliakas, Bianca Tesi, Jörg Cammenga, et al.
British Journal of Haematology|November 25, 2025
Comorbidities and mutations including single- and multihit TET2 mutations in relation to outcome in chronic myelomonocytic leukaemia-A population-based studyMatilda Kjellander Kynning, Ebba Westerberg, Linda Forsell, et al.
Pediatric Blood & Cancer|July 18, 2015
Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense MutationsBianca Tesi, Samuel C C Chiang, Dalia El-Ghoneimy, et al.
Annals of Internal Medicine|January 20, 2025
Germline <i>UBA1</i> Variant With Somatic Amplification in a Woman With Inflammatory Diseases and Myelodysplastic SyndromeMaria Creignou, Maria Sirenko, Pedro L Moura, et al.
Archivum Immunologiae Et Therapiae Experimentalis|October 22, 2021
Molecular Genetics Diversity of Primary Hemophagocytic Lymphohistiocytosis among Polish Pediatric PatientsKatarzyna Bąbol-Pokora, Magdalena Wołowiec, Katarzyna Popko, et al.
Immunity|March 19, 2015
Cytomegalovirus infection drives adaptive epigenetic diversification of NK cells with altered signaling and effector functionHeinrich Schlums, Frank Cichocki, Bianca Tesi, et al.
Frontiers in Medicine|August 14, 2023
Register-based and genetic studies of Prader-Willi syndrome show a high frequency of gonadal tumors and a possible mechanism for tumorigenesis through imprinting relaxationCarolina Maya-González, Sandra Wessman, Kristina Lagerstedt-Robinson, et al.
Pageof 7