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Bianca Tesi

Showing results (51-60 of 67) with videos related to

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Genome Medicine|December 20, 2015
Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosisBianca Tesi, Kristina Lagerstedt-Robinson, Samuel C C Chiang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 6, 2022
Genome sequencing is a sensitive first-line test to diagnose individuals with intellectual disabilityAnna Lindstrand, Marlene Ek, Malin Kvarnung, et al.
Frontiers in Genetics|July 7, 2025
Diagnostic yield of 1000 trio analyses with exome and genome sequencing in a clinical settingHelena Malmgren, Malin Kvarnung, Peter Gustafsson, et al.
Blood|March 23, 2023
The clinical picture of ERCC6L2 disease: from bone marrow failure to acute leukemiaMarja Hakkarainen, Ilse Kaaja, Suvi P M Douglas, et al.
European Journal of Medical Genetics|October 21, 2022
Genotype-phenotype associations in a large PTEN Hamartoma Tumor Syndrome (PHTS) patient cohortLinda A J Hendricks, Nicoline Hoogerbrugge, Hanka Venselaar, et al.
Blood|July 3, 2024
Efficacy of T-cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosisSamuel C C Chiang, Laura E Covill, Bianca Tesi, et al.
Nature Medicine|January 10, 2017
Targeting SAMHD1 with the Vpx protein to improve cytarabine therapy for hematological malignanciesNikolas Herold, Sean G Rudd, Linda Ljungblad, et al.
JCO Precision Oncology|June 29, 2023
Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With CancerElisabeth Wadensten, Sandra Wessman, Frida Abel, et al.
Haematologica|May 30, 2015
The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesisSebastian Fn Bode, Sandra Ammann, Waleed Al-Herz, et al.
Journal of the National Cancer Institute|September 29, 2022
Cancer risks by sex and variant type in PTEN hamartoma tumor syndromeLinda A J Hendricks, Nicoline Hoogerbrugge, Arjen R Mensenkamp, et al.
Pageof 7

Showing results (51-60 of 67) with videos related to

Sort By:
Pageof 7
Genome Medicine|December 20, 2015
Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosisBianca Tesi, Kristina Lagerstedt-Robinson, Samuel C C Chiang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 6, 2022
Genome sequencing is a sensitive first-line test to diagnose individuals with intellectual disabilityAnna Lindstrand, Marlene Ek, Malin Kvarnung, et al.
Frontiers in Genetics|July 7, 2025
Diagnostic yield of 1000 trio analyses with exome and genome sequencing in a clinical settingHelena Malmgren, Malin Kvarnung, Peter Gustafsson, et al.
Blood|March 23, 2023
The clinical picture of ERCC6L2 disease: from bone marrow failure to acute leukemiaMarja Hakkarainen, Ilse Kaaja, Suvi P M Douglas, et al.
European Journal of Medical Genetics|October 21, 2022
Genotype-phenotype associations in a large PTEN Hamartoma Tumor Syndrome (PHTS) patient cohortLinda A J Hendricks, Nicoline Hoogerbrugge, Hanka Venselaar, et al.
Blood|July 3, 2024
Efficacy of T-cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosisSamuel C C Chiang, Laura E Covill, Bianca Tesi, et al.
Nature Medicine|January 10, 2017
Targeting SAMHD1 with the Vpx protein to improve cytarabine therapy for hematological malignanciesNikolas Herold, Sean G Rudd, Linda Ljungblad, et al.
JCO Precision Oncology|June 29, 2023
Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With CancerElisabeth Wadensten, Sandra Wessman, Frida Abel, et al.
Haematologica|May 30, 2015
The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesisSebastian Fn Bode, Sandra Ammann, Waleed Al-Herz, et al.
Journal of the National Cancer Institute|September 29, 2022
Cancer risks by sex and variant type in PTEN hamartoma tumor syndromeLinda A J Hendricks, Nicoline Hoogerbrugge, Arjen R Mensenkamp, et al.
Pageof 7