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Manuela Germeshausen

Showing results (11-20 of 35) with videos related to

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Current Opinion in Hematology|November 30, 2006
Severe congenital neutropenia: inheritance and pathophysiologyJulia Skokowa, Manuela Germeshausen, Cornelia Zeidler, et al.
Current Opinion in Hematology|June 10, 2008
G-CSF receptor mutations in patients with congenital neutropeniaManuela Germeshausen, Julia Skokowa, Matthias Ballmaier, et al.
Journal of Pediatric Hematology/Oncology|September 29, 2012
A novel G6PC3 gene mutation in a patient with severe congenital neutropeniaCaner Aytekin, Manuela Germeshausen, Nilden Tuygun, et al.
British Journal of Haematology|December 15, 2005
Congenital amegakaryocytic thrombocytopenia: a retrospective clinical analysis of 20 patientsStephanie King, Manuela Germeshausen, Gabriele Strauss, et al.
European Journal of Pediatrics|February 24, 2010
Kostmann disease with developmental delay in three patientsCaner Aytekin, Manuela Germeshausen, Nilden Tuygun, et al.
Haematologica|March 12, 2010
Digenic mutations in severe congenital neutropeniaManuela Germeshausen, Cornelia Zeidler, Manfred Stuhrmann, et al.
Pediatric Blood & Cancer|April 30, 2013
Congenital amegakaryocytic thrombocytopenia (CAMT) presenting as severe pancytopenia in the first month of lifeMichael T Stoddart, Philip Connor, Manuela Germeshausen, et al.
European Journal of Pediatrics|February 19, 2010
Eponym. Kostmann diseaseCaner Aytekin, Manuela Germeshausen, Nilden Tuygun, et al.
Pediatric Transplantation|November 11, 2008
Unrelated cord blood transplantation in children with severe congenital neutropeniaM Akif Yesilipek, Gulsun Tezcan, Manuela Germeshausen, et al.
Human Mutation|March 7, 2013
The spectrum of ELANE mutations and their implications in severe congenital and cyclic neutropeniaManuela Germeshausen, Sabine Deerberg, Yvonne Peter, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Current Opinion in Hematology|November 30, 2006
Severe congenital neutropenia: inheritance and pathophysiologyJulia Skokowa, Manuela Germeshausen, Cornelia Zeidler, et al.
Current Opinion in Hematology|June 10, 2008
G-CSF receptor mutations in patients with congenital neutropeniaManuela Germeshausen, Julia Skokowa, Matthias Ballmaier, et al.
Journal of Pediatric Hematology/Oncology|September 29, 2012
A novel G6PC3 gene mutation in a patient with severe congenital neutropeniaCaner Aytekin, Manuela Germeshausen, Nilden Tuygun, et al.
British Journal of Haematology|December 15, 2005
Congenital amegakaryocytic thrombocytopenia: a retrospective clinical analysis of 20 patientsStephanie King, Manuela Germeshausen, Gabriele Strauss, et al.
European Journal of Pediatrics|February 24, 2010
Kostmann disease with developmental delay in three patientsCaner Aytekin, Manuela Germeshausen, Nilden Tuygun, et al.
Haematologica|March 12, 2010
Digenic mutations in severe congenital neutropeniaManuela Germeshausen, Cornelia Zeidler, Manfred Stuhrmann, et al.
Pediatric Blood & Cancer|April 30, 2013
Congenital amegakaryocytic thrombocytopenia (CAMT) presenting as severe pancytopenia in the first month of lifeMichael T Stoddart, Philip Connor, Manuela Germeshausen, et al.
European Journal of Pediatrics|February 19, 2010
Eponym. Kostmann diseaseCaner Aytekin, Manuela Germeshausen, Nilden Tuygun, et al.
Pediatric Transplantation|November 11, 2008
Unrelated cord blood transplantation in children with severe congenital neutropeniaM Akif Yesilipek, Gulsun Tezcan, Manuela Germeshausen, et al.
Human Mutation|March 7, 2013
The spectrum of ELANE mutations and their implications in severe congenital and cyclic neutropeniaManuela Germeshausen, Sabine Deerberg, Yvonne Peter, et al.
Pageof 4