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Journal Articles

Diagnostic Challenges in a Low a 2 β-Thalassemia Case

Niren Patel, MBBS, Natalia Dixon, MD, Lina Zhuang, MD, Shanequa Bryant, Ferdane Kutlar, MD, Abdullah Kutlar, MD

Blood (2014) 124 (21): 4898.

https://doi.org/10.1182/blood.V124.21.4898.4898

Published: 2014

Journal Articles

Homozygous Expression of a Novel Senegalese-Type Partial Deletion of the Beta and Delta Genes Causes a Delta 0 Beta + Thalassemia.

Hernan Sabio, MD, MS, Natalia Dixon, MD, Ferdane Kutlar, MD, Niren Patel, MBBS, Hanfang Zhang, MD, PhD, Lina Zhuang, MD, Abdullah Kutlar, MD

Blood (2012) 120 (21): 2128.

https://doi.org/10.1182/blood.V120.21.2128.2128

Published: 2012

Journal Articles

Diagnostic Complications of Thalassemic Hb Showa-Yakushiji (β110[G12] Leu→Pro),Observed in An African American Child with Co-Inherited Hb B 2 (δ16[A13]Gly→Arg) and α-Thal-2 (-α 3.7 deletion): Effects of Triple Globin Gene Abnormality On Phenotype.

Chinwe Obiaga, Niren Patel, MD, Hernan Sabio, MD, Natalia Dixon, MD, Steffen E. Meiler, MD, Lina Zhuang, MD, Abdullah Kutlar, MD, Ferdane Kutlar, MD

Blood (2009) 114 (22): 2558.

https://doi.org/10.1182/blood.V114.22.2558.2558

Published: 2009

Journal Articles

Recombinant Factor VIIa in the Management of Bleeding Associated with Congenital Factor V Deficiency.

Natalia Dixon, MD, Anita Smith, RN, CPNP, Hernan Sabio, MD

Blood (2009) 114 (22): 4444.

https://doi.org/10.1182/blood.V114.22.4444.4444

Published: 2009

Journal Articles

Efficacy of Hydroxyurea To Prevent Organ Damage in Young Children with Sickle Cell Anemia.

Courtney D. Thornburg, MD, MS, Natalia Dixon, MD, Shelly Burgett, FNP, Nicole A. Mortier, MHS, PA-C, Sherri A. Zimmerman, MD, Melanie J. Bonner, PhD, Agustin Calatroni, MA MS, Russell E. Ware, MD PhD

Blood (2007) 110 (11): 3386.

https://doi.org/10.1182/blood.V110.11.3386.3386

Published: 2007

NARROW

Diagnostic Challenges in a Low a 2 β-Thalassemia Case

Homozygous Expression of a Novel Senegalese-Type Partial Deletion of the Beta and Delta Genes Causes a Delta 0 Beta + Thalassemia.

Diagnostic Complications of Thalassemic Hb Showa-Yakushiji (β110[G12] Leu→Pro),Observed in An African American Child with Co-Inherited Hb B 2 (δ16[A13]Gly→Arg) and α-Thal-2 (-α 3.7 deletion): Effects of Triple Globin Gene Abnormality On Phenotype.

Recombinant Factor VIIa in the Management of Bleeding Associated with Congenital Factor V Deficiency.

Efficacy of Hydroxyurea To Prevent Organ Damage in Young Children with Sickle Cell Anemia.

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ASH Publications

American Society of Hematology

Diagnostic Challenges in a Low a 2 β-Thalassemia Case

Homozygous Expression of a Novel Senegalese-Type Partial Deletion of the Beta and Delta Genes Causes a Delta 0 Beta + Thalassemia.

Diagnostic Complications of Thalassemic Hb Showa-Yakushiji (β110[G12] Leu→Pro),Observed in An African American Child with Co-Inherited Hb B 2 (δ16[A13]Gly→Arg) and α-Thal-2 (-α 3.7 deletion): Effects of Triple Globin Gene Abnormality On Phenotype.

Recombinant Factor VIIa in the Management of Bleeding Associated with Congenital Factor V Deficiency.

Efficacy of Hydroxyurea To Prevent Organ Damage in Young Children with Sickle Cell Anemia.

Email alerts

ASH Publications

American Society of Hematology

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