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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 Challenge Presented by “Hb F only” Pattern In Newborn Screening for Hemoglobinopathies: Approach to Accurate Diagnosis

Niren Patel, MBBS, Hanfang Zhang, MD, PhD, Lina Zhuang, MD, Rupa Redding-Lallinger, MD, Ruth Luddy, MD, Abdullah Kutlar, MD, Ferdane Kutlar, MD

Blood (2010) 116 (21): 5173.

https://doi.org/10.1182/blood.V116.21.5173.5173

Published: 2010

Journal Articles

The Quest for Hb Questembert: A Challenging Case of An Unstable Hb Variant

Kavita Natarajan, Niren Patel, MBBS, Lina Zhuang, MD, Harris Carmichael, Elizabeth Manaloor, MD, Abdullah Kutlar, MD, Ferdane Kutlar, MD

Blood (2010) 116 (21): 4814.

https://doi.org/10.1182/blood.V116.21.4814.4814

Published: 2010

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

Hb Dothan [β25/26 (B7/B8)/(-GTG/-GLY)/Gly+Glu→Glu]; A Novel Mechanism Leading to a M-Hemoglobin.

Ferdane Kutlar, MD, Lee Hilliard, MD, Lina Zhuang, MD, Niren Patel, MBBS, Abdullah Kutlar, MD

Blood (2008) 112 (11): 1440.

https://doi.org/10.1182/blood.V112.11.1440.1440

Published: 2008

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 Challenge Presented by “Hb F only” Pattern In Newborn Screening for Hemoglobinopathies: Approach to Accurate Diagnosis

The Quest for Hb Questembert: A Challenging Case of An Unstable Hb Variant

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.

Hb Dothan [β25/26 (B7/B8)/(-GTG/-GLY)/Gly+Glu→Glu]; A Novel Mechanism Leading to a M-Hemoglobin.

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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 Challenge Presented by “Hb F only” Pattern In Newborn Screening for Hemoglobinopathies: Approach to Accurate Diagnosis

The Quest for Hb Questembert: A Challenging Case of An Unstable Hb Variant

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.

Hb Dothan [β25/26 (B7/B8)/(-GTG/-GLY)/Gly+Glu→Glu]; A Novel Mechanism Leading to a M-Hemoglobin.

Email alerts

ASH Publications

American Society of Hematology

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