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Cornelia Zeidler

Showing results (41-50 of 54) with videos related to

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Haematologica|July 6, 2014
Outcome and management of pregnancies in severe chronic neutropenia patients by the European Branch of the Severe Chronic Neutropenia International RegistryCornelia Zeidler, Ulrike A H Grote, Anna Nickel, et al.
Nature Genetics|December 26, 2006
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)Christoph Klein, Magda Grudzien, Giridharan Appaswamy, et al.
Current Opinion in Hematology|November 20, 2018
Neutropenia in glycogen storage disease Ib: outcomes for patients treated with granulocyte colony-stimulating factorDavid C Dale, Audrey Anna Bolyard, Tracy Marrero, et al.
Haematologica|March 27, 2025
Genetic and clinical characteristics of patients with Shwachman Diamond syndrome with special consideration of treatment with granulocyte-colony stimulating factorSabine Mellor-Heineke, Julia Skokowa, Natali Gerschmann, et al.
Haematologica|June 29, 2019
CRISPR/Cas9-mediated <i>ELANE</i> knockout enables neutrophilic maturation of primary hematopoietic stem and progenitor cells and induced pluripotent stem cells of severe congenital neutropenia patientsMasoud Nasri, Malte Ritter, Perihan Mir, et al.
Hemasphere|April 17, 2025
European guidelines on treatment and supportive measures in chronic neutropenias: A consensus between the European Hematology Association and the EuNet-INNOCHRON COST Action based on a systematic evidence reviewFrancesca Fioredda, Michail Spanoudakis, Julia Skokowa, et al.
Cell Stem Cell|April 24, 2021
iPSC modeling of stage-specific leukemogenesis reveals BAALC as a key oncogene in severe congenital neutropeniaBenjamin Dannenmann, Maksim Klimiankou, Benedikt Oswald, et al.
Blood Advances|January 8, 2025
Extended clinical phenotypes and treatment modalities in 32 JAGN1-deficient patients: a multicenter study by ESID and EBMT IEWPJulia Fekadu-Siebald, Emilia Salzmann-Manrique, Jan Robert Heusel, et al.
The New England Journal of Medicine|January 2, 2009
A syndrome with congenital neutropenia and mutations in G6PC3Kaan Boztug, Giridharan Appaswamy, Angel Ashikov, et al.
Blood|December 6, 2024
A new severe congenital neutropenia syndrome associated with autosomal recessive COPZ1 mutationsNatalia Borbaran Bravo, Ekaterina Deordieva, Larissa Doll, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Haematologica|July 6, 2014
Outcome and management of pregnancies in severe chronic neutropenia patients by the European Branch of the Severe Chronic Neutropenia International RegistryCornelia Zeidler, Ulrike A H Grote, Anna Nickel, et al.
Nature Genetics|December 26, 2006
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)Christoph Klein, Magda Grudzien, Giridharan Appaswamy, et al.
Current Opinion in Hematology|November 20, 2018
Neutropenia in glycogen storage disease Ib: outcomes for patients treated with granulocyte colony-stimulating factorDavid C Dale, Audrey Anna Bolyard, Tracy Marrero, et al.
Haematologica|March 27, 2025
Genetic and clinical characteristics of patients with Shwachman Diamond syndrome with special consideration of treatment with granulocyte-colony stimulating factorSabine Mellor-Heineke, Julia Skokowa, Natali Gerschmann, et al.
Haematologica|June 29, 2019
CRISPR/Cas9-mediated <i>ELANE</i> knockout enables neutrophilic maturation of primary hematopoietic stem and progenitor cells and induced pluripotent stem cells of severe congenital neutropenia patientsMasoud Nasri, Malte Ritter, Perihan Mir, et al.
Hemasphere|April 17, 2025
European guidelines on treatment and supportive measures in chronic neutropenias: A consensus between the European Hematology Association and the EuNet-INNOCHRON COST Action based on a systematic evidence reviewFrancesca Fioredda, Michail Spanoudakis, Julia Skokowa, et al.
Cell Stem Cell|April 24, 2021
iPSC modeling of stage-specific leukemogenesis reveals BAALC as a key oncogene in severe congenital neutropeniaBenjamin Dannenmann, Maksim Klimiankou, Benedikt Oswald, et al.
Blood Advances|January 8, 2025
Extended clinical phenotypes and treatment modalities in 32 JAGN1-deficient patients: a multicenter study by ESID and EBMT IEWPJulia Fekadu-Siebald, Emilia Salzmann-Manrique, Jan Robert Heusel, et al.
The New England Journal of Medicine|January 2, 2009
A syndrome with congenital neutropenia and mutations in G6PC3Kaan Boztug, Giridharan Appaswamy, Angel Ashikov, et al.
Blood|December 6, 2024
A new severe congenital neutropenia syndrome associated with autosomal recessive COPZ1 mutationsNatalia Borbaran Bravo, Ekaterina Deordieva, Larissa Doll, et al.
Pageof 6