Page 1 | Search Results | Blood | American Society of Hematology

1-6 of 6

Sort by

Sort Order Select

Journal Articles

A novel type of congenital hypochromic anemia associated with a nonsense mutation in the STEAP3/TSAP6 gene

Bernard Grandchamp, Gilles Hetet, Caroline Kannengiesser, Claire Oudin, Carole Beaumont, Sylvie Rodrigues-Ferreira, Robert Amson, Adam Telerman, Peter Nielsen, Elisabeth Kohne, Christina Balser, Hermann Heimpel

Blood (2011) 118 (25): 6660–6666.

https://doi.org/10.1182/blood-2011-01-329011

Published: 2011

Includes: Supplemental data

Journal Articles

Dihydrofolate Reductase Deficiency Is Caused by a Homozygous DHFR Mutation and Leads to Congenital Megaloblastic Anemia and Cerebral Folate Deficiency

Holger Cario, MD, Desiree E.C. Smith, PhD, Henk J. Blom, PhD, Harald Bode, MD, Nenad Blau, PhD, Karlheinz Holzmann, PhD, Ulrich Pannicke, Elisabeth Kohne, MD, Klaus-Michael Debatin, MD, Yvo M. Smulders, MD, Klaus Schwarz

Blood (2010) 116 (21): 1006.

https://doi.org/10.1182/blood.V116.21.1006.1006

Published: 2010

Journal Articles

Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation

Hermann Heimpel, Klaus Schwarz, Monika Ebnöther, Jeroen S. Goede, Detlev Heydrich, Torsten Kamp, Lothar Plaumann, Bettina Rath, Jochen Roessler, Otto Schildknecht, Mathias Schmid, Walter Wuillemin, Beate Einsiedler, Rosi Leichtle, Hannah Tamary, Elisabeth Kohne

Blood (2006) 107 (1): 334–340.

https://doi.org/10.1182/blood-2005-01-0421

Published: 2006

Journal Articles

Clinical and Molecular Findings in Childhood Polycythemia Vera.

Holger Cario, MD, Heike L. Pahl, PhD, Minkov Milen, MD, Reinhard Harald, MD, Elisabeth Kohne, MD, Klaus-Michael Debatin, MD

Blood (2005) 106 (11): 4961.

https://doi.org/10.1182/blood.V106.11.4961.4961

Published: 2005

Journal Articles

Congenital dyserythropoietic anemia type II: epidemiology, clinical appearance, and prognosis based on long-term observation

Hermann Heimpel, Volker Anselstetter, Ladislav Chrobak, Jonas Denecke, Beate Einsiedler, Kerstin Gallmeier, Antje Griesshammer, Thorsten Marquardt, Gritta Janka-Schaub, Martina Kron, Elisabeth Kohne

Blood (2003) 102 (13): 4576–4581.

https://doi.org/10.1182/blood-2003-02-0613

Published: 2003

Journal Articles

von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP

Reinhard Schneppenheim, Ulrich Budde, Florian Oyen, Dorothea Angerhaus, Volker Aumann, Elke Drewke, Wolf Hassenpflug, Johannes Häberle, Karim Kentouche, Elisabeth Kohne, Karin Kurnik, Dirk Mueller-Wiefel, Tobias Obser, René Santer, Karl-Walter Sykora

Blood (2003) 101 (5): 1845–1850.

https://doi.org/10.1182/blood-2002-08-2399

Published: 2003

NARROW

A novel type of congenital hypochromic anemia associated with a nonsense mutation in the STEAP3/TSAP6 gene

Dihydrofolate Reductase Deficiency Is Caused by a Homozygous DHFR Mutation and Leads to Congenital Megaloblastic Anemia and Cerebral Folate Deficiency

Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation

Clinical and Molecular Findings in Childhood Polycythemia Vera.

Congenital dyserythropoietic anemia type II: epidemiology, clinical appearance, and prognosis based on long-term observation

von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP

Email alerts

ASH Publications

American Society of Hematology

A novel type of congenital hypochromic anemia associated with a nonsense mutation in the STEAP3/TSAP6 gene

Dihydrofolate Reductase Deficiency Is Caused by a Homozygous DHFR Mutation and Leads to Congenital Megaloblastic Anemia and Cerebral Folate Deficiency

Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation

Clinical and Molecular Findings in Childhood Polycythemia Vera.

Congenital dyserythropoietic anemia type II: epidemiology, clinical appearance, and prognosis based on long-term observation

von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only