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Journal Articles

Clinical Characterization of a Novel Mutation in SLC25A38 Resulting in Congenital Sideroblastic Anemia in a Canadian First Nations Population

Kelsey Uminski, MD BSc, Donald S. Houston, MD PhD, Jessica Hartley, MS, CGC, Geoffrey Cuvelier, MD, Sara J. Israels, MD

Blood (2018) 132 (Supplement 1): 1035.

https://doi.org/10.1182/blood-2018-99-110343

Published: 2018

Journal Articles

Copper Deficiency

Allison Close, MD, Lynn M. Malec, MD MSc

Blood (2017) 130 (Supplement 1): 4742.

https://doi.org/10.1182/blood.V130.Suppl_1.4742.4742

Published: 2017

Journal Articles

Glucose Phosphate Isomerase Deficiency In 2 Patients With Novel Mutations Presenting As Severe Neurologic Abnormalities and Transfusion Dependent Hemolytic Anemia

Mammen Puliyel, M.B., B.S., Patrick G. Gallagher, MD, Vasilios Berdoukas, MBBS, Bertil Glader, MD, PhD, Thomas Coates, MD

Blood (2013) 122 (21): 947.

https://doi.org/10.1182/blood.V122.21.947.947

Published: 2013

Journal Articles

Thrombocytopenia and Platelet Ultra-Structural Abnormalities Associated with RUNX1 Haploinsufficiency in Monosomy 21 Mosaicism.

Riten Kumar, MD, MSc, Fred Pluthero, PhD, Hilary Christensen, Walter H. Kahr, MD, PhD

Blood (2012) 120 (21): 2190.

https://doi.org/10.1182/blood.V120.21.2190.2190

Published: 2012

Journal Articles

Prospective Analysis of Bruising in Children with and without an Inherited Bleeding Disorder.

M. Hamilton, B. Jenkins, F. Dunstan, A. Kemp, R. Liesner, E. Chalmers, J. Hanley, A. Jungmann, A. Thomas, P. Collins

Blood (2006) 108 (11): 1024.

https://doi.org/10.1182/blood.V108.11.1024.1024

Published: 2006

NARROW

Clinical Characterization of a Novel Mutation in SLC25A38 Resulting in Congenital Sideroblastic Anemia in a Canadian First Nations Population

Copper Deficiency

Glucose Phosphate Isomerase Deficiency In 2 Patients With Novel Mutations Presenting As Severe Neurologic Abnormalities and Transfusion Dependent Hemolytic Anemia

Thrombocytopenia and Platelet Ultra-Structural Abnormalities Associated with RUNX1 Haploinsufficiency in Monosomy 21 Mosaicism.

Prospective Analysis of Bruising in Children with and without an Inherited Bleeding Disorder.

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ASH Publications

American Society of Hematology

Clinical Characterization of a Novel Mutation in SLC25A38 Resulting in Congenital Sideroblastic Anemia in a Canadian First Nations Population

Copper Deficiency

Glucose Phosphate Isomerase Deficiency In 2 Patients With Novel Mutations Presenting As Severe Neurologic Abnormalities and Transfusion Dependent Hemolytic Anemia

Thrombocytopenia and Platelet Ultra-Structural Abnormalities Associated with RUNX1 Haploinsufficiency in Monosomy 21 Mosaicism.

Prospective Analysis of Bruising in Children with and without an Inherited Bleeding Disorder.

Email alerts

ASH Publications

American Society of Hematology

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