Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Hermann Heimpel

Showing results (21-30 of 36) with videos related to

Pageof 4
Sort By:
Annals of Hematology|April 1, 2009
Bulky extramedullary hematopoiesis is not a rare complication of congenital dyserythropoietic anemiaHermann Heimpel, Ulrich Dührsen, P Hofbauer, et al.
Hemoglobin|November 17, 2010
A dyserythropoietic anemia associated with homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), a variant with an unstable α chainLoïc Garçon, Achille Iolascon, Serge Pissard, et al.
Advances in Experimental Medicine and Biology|September 9, 2010
Epidemiology of rare anaemias in EuropeBeatrice Gulbis, Androulla Eleftheriou, Michael Angastiniotis, et al.
Blood|June 30, 2005
The Jak2V617F mutation, PRV-1 overexpression, and EEC formation define a similar cohort of MPD patientsPhilipp S Goerttler, Cordula Steimle, Edith März, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 9, 2011
Growth differentiation factor 15 in patients with congenital dyserythropoietic anaemia (CDA) type IIGuillem Casanovas, Dorine W Swinkels, Sandro Altamura, et al.
Blood|August 23, 2003
Congenital dyserythropoietic anemia type II: epidemiology, clinical appearance, and prognosis based on long-term observationHermann Heimpel, Volker Anselstetter, Ladislav Chrobak, et al.
British Journal of Haematology|July 30, 2016
Analysis of a cohort of 101 CDAII patients: description of 24 new molecular variants and genotype-phenotype correlationsPaola Bianchi, Klaus Schwarz, Josef Högel, et al.
Blood|October 28, 2011
A novel type of congenital hypochromic anemia associated with a nonsense mutation in the STEAP3/TSAP6 geneBernard Grandchamp, Gilles Hetet, Caroline Kannengiesser, et al.
Blood|August 2, 2003
Quantification of PRV-1 mRNA distinguishes polycythemia vera from secondary erythrocytosisSteffen Klippel, Elisabeth Strunck, Snezana Temerinac, et al.
Blood|September 6, 2005
Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observationHermann Heimpel, Klaus Schwarz, Monika Ebnöther, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Annals of Hematology|April 1, 2009
Bulky extramedullary hematopoiesis is not a rare complication of congenital dyserythropoietic anemiaHermann Heimpel, Ulrich Dührsen, P Hofbauer, et al.
Hemoglobin|November 17, 2010
A dyserythropoietic anemia associated with homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), a variant with an unstable α chainLoïc Garçon, Achille Iolascon, Serge Pissard, et al.
Advances in Experimental Medicine and Biology|September 9, 2010
Epidemiology of rare anaemias in EuropeBeatrice Gulbis, Androulla Eleftheriou, Michael Angastiniotis, et al.
Blood|June 30, 2005
The Jak2V617F mutation, PRV-1 overexpression, and EEC formation define a similar cohort of MPD patientsPhilipp S Goerttler, Cordula Steimle, Edith März, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 9, 2011
Growth differentiation factor 15 in patients with congenital dyserythropoietic anaemia (CDA) type IIGuillem Casanovas, Dorine W Swinkels, Sandro Altamura, et al.
Blood|August 23, 2003
Congenital dyserythropoietic anemia type II: epidemiology, clinical appearance, and prognosis based on long-term observationHermann Heimpel, Volker Anselstetter, Ladislav Chrobak, et al.
British Journal of Haematology|July 30, 2016
Analysis of a cohort of 101 CDAII patients: description of 24 new molecular variants and genotype-phenotype correlationsPaola Bianchi, Klaus Schwarz, Josef Högel, et al.
Blood|October 28, 2011
A novel type of congenital hypochromic anemia associated with a nonsense mutation in the STEAP3/TSAP6 geneBernard Grandchamp, Gilles Hetet, Caroline Kannengiesser, et al.
Blood|August 2, 2003
Quantification of PRV-1 mRNA distinguishes polycythemia vera from secondary erythrocytosisSteffen Klippel, Elisabeth Strunck, Snezana Temerinac, et al.
Blood|September 6, 2005
Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observationHermann Heimpel, Klaus Schwarz, Monika Ebnöther, et al.
Pageof 4