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Manuela Germeshausen

Showing results (1-10 of 35) with videos related to

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British Journal of Haematology|April 25, 2009
Advances in the understanding of congenital amegakaryocytic thrombocytopeniaMatthias Ballmaier, Manuela Germeshausen
Best Practice & Research. Clinical Haematology|August 18, 2021
Congenital amegakaryocytic thrombocytopenia - Not a single diseaseManuela Germeshausen, Matthias Ballmaier
Seminars in Thrombosis and Hemostasis|November 22, 2011
Congenital amegakaryocytic thrombocytopenia: clinical presentation, diagnosis, and treatmentMatthias Ballmaier, Manuela Germeshausen
Haematologica|July 25, 2020
CAMT-MPL: congenital amegakaryocytic thrombocytopenia caused by MPL mutations - heterogeneity of a monogenic disorder - a comprehensive analysis of 56 patientsManuela Germeshausen, Matthias Ballmaier
Blood|September 21, 2006
Incidence of CSF3R mutations in severe congenital neutropenia and relevance for leukemogenesis: Results of a long-term surveyManuela Germeshausen, Matthias Ballmaier, Karl Welte
Human Mutation|February 14, 2006
MPL mutations in 23 patients suffering from congenital amegakaryocytic thrombocytopenia: the type of mutation predicts the course of the diseaseManuela Germeshausen, Matthias Ballmaier, Karl Welte
Blood|November 21, 2008
In vivo expansion of cells expressing acquired CSF3R mutations in patients with severe congenital neutropeniaManuela Germeshausen, Karl Welte, Matthias Ballmaier
Hamostaseologie|November 2, 2023
THROMKIDplus Patient Registry and Biomaterial Banking for Children with Inherited Platelet DisordersMatthias Ballmaier, Manuela Germeshausen, Harald Schulze, et al.
British Journal of Haematology|January 6, 2009
Clinical implications of ELA2-, HAX1-, and G-CSF-receptor (CSF3R) mutations in severe congenital neutropeniaCornelia Zeidler, Manuela Germeshausen, Christoph Klein, et al.
European Journal of Haematology|April 23, 2014
A novel G6PC3 gene mutation in severe congenital neutropenia: pancytopenia and variable bone marrow phenotype can also be part of this syndromeTugba Arikoglu, Necdet Kuyucu, Manuela Germeshausen, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
British Journal of Haematology|April 25, 2009
Advances in the understanding of congenital amegakaryocytic thrombocytopeniaMatthias Ballmaier, Manuela Germeshausen
Best Practice & Research. Clinical Haematology|August 18, 2021
Congenital amegakaryocytic thrombocytopenia - Not a single diseaseManuela Germeshausen, Matthias Ballmaier
Seminars in Thrombosis and Hemostasis|November 22, 2011
Congenital amegakaryocytic thrombocytopenia: clinical presentation, diagnosis, and treatmentMatthias Ballmaier, Manuela Germeshausen
Haematologica|July 25, 2020
CAMT-MPL: congenital amegakaryocytic thrombocytopenia caused by MPL mutations - heterogeneity of a monogenic disorder - a comprehensive analysis of 56 patientsManuela Germeshausen, Matthias Ballmaier
Blood|September 21, 2006
Incidence of CSF3R mutations in severe congenital neutropenia and relevance for leukemogenesis: Results of a long-term surveyManuela Germeshausen, Matthias Ballmaier, Karl Welte
Human Mutation|February 14, 2006
MPL mutations in 23 patients suffering from congenital amegakaryocytic thrombocytopenia: the type of mutation predicts the course of the diseaseManuela Germeshausen, Matthias Ballmaier, Karl Welte
Blood|November 21, 2008
In vivo expansion of cells expressing acquired CSF3R mutations in patients with severe congenital neutropeniaManuela Germeshausen, Karl Welte, Matthias Ballmaier
Hamostaseologie|November 2, 2023
THROMKIDplus Patient Registry and Biomaterial Banking for Children with Inherited Platelet DisordersMatthias Ballmaier, Manuela Germeshausen, Harald Schulze, et al.
British Journal of Haematology|January 6, 2009
Clinical implications of ELA2-, HAX1-, and G-CSF-receptor (CSF3R) mutations in severe congenital neutropeniaCornelia Zeidler, Manuela Germeshausen, Christoph Klein, et al.
European Journal of Haematology|April 23, 2014
A novel G6PC3 gene mutation in severe congenital neutropenia: pancytopenia and variable bone marrow phenotype can also be part of this syndromeTugba Arikoglu, Necdet Kuyucu, Manuela Germeshausen, et al.
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