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Manuela Germeshausen

Showing results (31-40 of 35) with videos related to

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British Journal of Haematology|November 28, 2008
Familial thrombocytosis caused by the novel germ-line mutation p.Pro106Leu in the MPL geneEl-Harith Abdelghaffar El-Harith, Cornelia Roesl, Matthias Ballmaier, 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.
Nature Genetics|December 26, 2006
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)Christoph Klein, Magda Grudzien, Giridharan Appaswamy, 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|April 17, 2016
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disordersIlenia Simeoni, Jonathan C Stephens, Fengyuan Hu, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
British Journal of Haematology|November 28, 2008
Familial thrombocytosis caused by the novel germ-line mutation p.Pro106Leu in the MPL geneEl-Harith Abdelghaffar El-Harith, Cornelia Roesl, Matthias Ballmaier, 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.
Nature Genetics|December 26, 2006
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)Christoph Klein, Magda Grudzien, Giridharan Appaswamy, 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|April 17, 2016
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disordersIlenia Simeoni, Jonathan C Stephens, Fengyuan Hu, et al.
Pageof 4