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Karl Welte

Showing results (121-130 of 148) with videos related to

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Current Opinion in Hematology|November 27, 2014
The diversity of mutations and clinical outcomes for ELANE-associated neutropeniaVahagn Makaryan, Cornelia Zeidler, Audrey Anna Bolyard, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 22, 2010
Granulocyte colony-stimulating factor (G-CSF) treatment of childhood acute myeloid leukemias that overexpress the differentiation-defective G-CSF receptor isoform IV is associated with a higher incidence of relapseStephanie Ehlers, Christin Herbst, Martin Zimmermann, et al.
Hemasphere|July 11, 2020
Congenital and Acquired Chronic Neutropenias: Challenges, Perspectives and Implementation of the EuNet-INNOCHRON ActionHelen A Papadaki, Irene Mavroudi, Antonio Almeida, et al.
Hemasphere|April 3, 2023
The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST ActionFrancesca Fioredda, Julia Skokowa, Hannah Tamary, et al.
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.
Human Mutation|April 23, 2014
TCIRG1-associated congenital neutropeniaVahagn Makaryan, Elisabeth A Rosenthal, Audrey Anna Bolyard, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 31, 2025
Tuning of G-CSFR signaling by de novo designed agonistsTimo Ullrich, Christoph Pollmann, Malte Ritter, et al.
Leukemia|November 4, 2021
A unique role of p53 haploinsufficiency or loss in the development of acute myeloid leukemia with FLT3-ITD mutationMin Yang, Zengkai Pan, Kezhi Huang, 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.
Pageof 15

Showing results (121-130 of 148) with videos related to

Sort By:
Pageof 15
Current Opinion in Hematology|November 27, 2014
The diversity of mutations and clinical outcomes for ELANE-associated neutropeniaVahagn Makaryan, Cornelia Zeidler, Audrey Anna Bolyard, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 22, 2010
Granulocyte colony-stimulating factor (G-CSF) treatment of childhood acute myeloid leukemias that overexpress the differentiation-defective G-CSF receptor isoform IV is associated with a higher incidence of relapseStephanie Ehlers, Christin Herbst, Martin Zimmermann, et al.
Hemasphere|July 11, 2020
Congenital and Acquired Chronic Neutropenias: Challenges, Perspectives and Implementation of the EuNet-INNOCHRON ActionHelen A Papadaki, Irene Mavroudi, Antonio Almeida, et al.
Hemasphere|April 3, 2023
The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST ActionFrancesca Fioredda, Julia Skokowa, Hannah Tamary, et al.
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.
Human Mutation|April 23, 2014
TCIRG1-associated congenital neutropeniaVahagn Makaryan, Elisabeth A Rosenthal, Audrey Anna Bolyard, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 31, 2025
Tuning of G-CSFR signaling by de novo designed agonistsTimo Ullrich, Christoph Pollmann, Malte Ritter, et al.
Leukemia|November 4, 2021
A unique role of p53 haploinsufficiency or loss in the development of acute myeloid leukemia with FLT3-ITD mutationMin Yang, Zengkai Pan, Kezhi Huang, 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.
Pageof 15