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Journal Articles

Coinheritance of Alpha -3.7 Deletion and Hb Questembert [ 131 alpha-2 Tct > CCT](Ser131>Pro)] in an African American Patient Results in an Alpha Thalassemia Phenotype

Asiya Shakir, MD, Betty Pace, MD, Niren Patel, MBBS, Ferdane Kutlar, MD, Abdullah Kutlar, MD, Afshin Ameri, MD

Blood (2015) 126 (23): 4597.

https://doi.org/10.1182/blood.V126.23.4597.4597

Published: 2015

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

Improving the Accuracy of BCR-ABL Transcript Quantitation: Pitfalls of Using a Common Standard for b3a2 and b2a2 Transcripts

Hanfang Zhang, MD, PhD, Linda Fletcher, Niren Patel, MBBS, Shanequa Bryant, Honglin Li, PhD, Ferdane Kutlar, MD, Anand P. Jillella, MD, Vamsi Kota, MBBS, Betsy Clair, Abdullah Kutlar, MD

Blood (2012) 120 (21): 4423.

https://doi.org/10.1182/blood.V120.21.4423.4423

Published: 2012

Journal Articles

Exploratory Study of Haptoglobin Levels by Genotype in Adult Sickle Cell Patients

Harrison C. Brown, BBA, Ferdane Kutlar, MD, Betsy Clair, Abdullah Kutlar, MD

Blood (2011) 118 (21): 2145.

https://doi.org/10.1182/blood.V118.21.2145.2145

Published: 2011

Journal Articles

BCL11A Polymorphism and HbF Response to Hydroxyurea in Adult Patients with Sickle Cell Disease

Philip Sobash, Ferdane Kutlar, MD, Harrison C. Brown, BBA, Betsy Clair, Abdullah Kutlar, MD

Blood (2011) 118 (21): 1051.

https://doi.org/10.1182/blood.V118.21.1051.1051

Published: 2011

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

Potential Pitfalls In Quantitative Real-Time PCR for Molecular Monitoring of BCR-ABL In the Management of CML.

Hanfang Zhang, MD, PhD, Niren Patel, MBBS, Ferdane Kutlar, MD, Anand P. Jillella, MD, Celalettin Ustun, MD, Leigh G Wells, MSN, RN, FNP-BC, Betsy Clair, Abdullah Kutlar, MD

Blood (2010) 116 (21): 1228.

https://doi.org/10.1182/blood.V116.21.1228.1228

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

Pomalidomide Modifies Sickle Cell Related Organ Damage in Transgenic Mice with Sickle Cell Anemia.

Steffen E. Meiler, MD, Marlene Wade, Laure Moutouh de Parseval, MD, Laura G Corral, Paul S. Swerdlow, MD, Ferdane Kutlar, MD, Abdullah Kutlar

Blood (2009) 114 (22): 904.

https://doi.org/10.1182/blood.V114.22.904.904

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

Journal Articles

In Vitro Exploratory Studies of Haptoglobin Polymorphisms and Their Effect on Cytokine Release from Cultured Mononuclear Cells in Sickle Cell Disease.

Komal Bora, Kavita Natarajan, MBBS, Ferdane Kutlar, MD, Hanfang Zhang, MD, PhD, Hongyan Xu, PhD, Betsy Clair, Kathleen M McKie, MD, Abdullah Kutlar, MD

Blood (2008) 112 (11): 1441.

https://doi.org/10.1182/blood.V112.11.1441.1441

Published: 2008

Journal Articles

Candidate Gene Polymorphisms and Their Association with TCD Velocities in Children with Sickle Cell Disease.

Abdullah Kutlar, MD, Donald Brambilla, PhD, Betsy Clair, Anne Haghighat, Sule Bakanay, MD, Gaye Adams, MD, Ferdane Kutlar, MD, Virgil McKie, MD, Beatrice Files, MD, Gerald Woods, MD, Melanie Kirby, MD, Elliott Vichinsky, MD, Clark Brown, MD, Charles Scher, MD, Robert Adams, MD

Blood (2007) 110 (11): 429.

https://doi.org/10.1182/blood.V110.11.429.429

Published: 2007

Journal Articles

Heat Shock Protein Inhibition in Sickle Cell Disease: A Novel Approach to Attenuating the Inflammatory Response?.

Kavita Natarajan, MBBS, John Catravas, PhD, Joseph Cannon, PhD, Tao Li, MD, Ferdane Kutlar, MD, Gloria Sloan, Sabine Fields, RN, Betsy Clair, Abdullah Kutlar, MD

Blood (2007) 110 (11): 2263.

https://doi.org/10.1182/blood.V110.11.2263.2263

Published: 2007

Journal Articles

Missense Mutation of the Last Nucleotide of Exon 1 of β-globin Gene Interferes with the Expression of Wild Allele.

Neeraj Agarwal, MD, Ferdane Kutlar, MD, Scott Reading, PhD, Abdullah Kutlar, MD, Josef Prchal, MD

Blood (2007) 110 (11): 1777.

https://doi.org/10.1182/blood.V110.11.1777.1777

Published: 2007

Journal Articles

A Case of HPP with a Novel Combination of α and β Spectrin Mutations.

Kavita Natarajan, MBBS, Ferdane Kutlar, MD, Tao Li, MD, Patrick Gallagher, MD, Abdullah Kutlar, MD

Blood (2007) 110 (11): 1736.

https://doi.org/10.1182/blood.V110.11.1736.1736

Published: 2007

Journal Articles

The Occurrence of Four Globin Abnormalities in One Individual: Hb SC Disease with Hb Chicago and Deletional Alpha Thalassemia.

Heather Hughes, Ferdane Kutlar, MD, Kathleen M. McKie, MD, Leslie Holley, Dedrey Elam, Abdullah Kutlar, MD

Blood (2007) 110 (11): 3802.

https://doi.org/10.1182/blood.V110.11.3802.3802

Published: 2007

Journal Articles

Novel Mechanism of β0 Thalassemia: Missense Mutation of the Last Nucleotide of β Globin Exon 1 (G->C) Leads to Undetectable Transcript and Mutant Peptide.

Neeraj Agarwal, MD, Mariluz P. Mojica-Henshaw, MD, PhD, Ferdane Kutlar, MD, Amos Gaikwad, MD, Ching N. Ou, PhD, Abdullah Kutlar, MD, Josef T. Prchal, MD

Blood (2006) 108 (11): 1598.

https://doi.org/10.1182/blood.V108.11.1598.1598

Published: 2006

Journal Articles

Mu Opioid Receptor (OPRM-1) Polymorphisms among Patients with Sickle Cell Disease.

Sharmila Mehta, MD, Nicholas Campbell, Lakiea Bailey, Ferdane Kutlar, MD, Dedrey Elam, Betsy Clair, Abdullah Kutlar, MD

Blood (2005) 106 (11): 3804.

https://doi.org/10.1182/blood.V106.11.3804.3804

Published: 2005

NARROW

Coinheritance of Alpha -3.7 Deletion and Hb Questembert [ 131 alpha-2 Tct > CCT](Ser131>Pro)] in an African American Patient Results in an Alpha Thalassemia Phenotype

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.

Improving the Accuracy of BCR-ABL Transcript Quantitation: Pitfalls of Using a Common Standard for b3a2 and b2a2 Transcripts

Exploratory Study of Haptoglobin Levels by Genotype in Adult Sickle Cell Patients

BCL11A Polymorphism and HbF Response to Hydroxyurea in Adult Patients with Sickle Cell Disease

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

Potential Pitfalls In Quantitative Real-Time PCR for Molecular Monitoring of BCR-ABL In the Management of CML.

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.

Pomalidomide Modifies Sickle Cell Related Organ Damage in Transgenic Mice with Sickle Cell Anemia.

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

In Vitro Exploratory Studies of Haptoglobin Polymorphisms and Their Effect on Cytokine Release from Cultured Mononuclear Cells in Sickle Cell Disease.

Candidate Gene Polymorphisms and Their Association with TCD Velocities in Children with Sickle Cell Disease.

Heat Shock Protein Inhibition in Sickle Cell Disease: A Novel Approach to Attenuating the Inflammatory Response?.

Missense Mutation of the Last Nucleotide of Exon 1 of β-globin Gene Interferes with the Expression of Wild Allele.

A Case of HPP with a Novel Combination of α and β Spectrin Mutations.

The Occurrence of Four Globin Abnormalities in One Individual: Hb SC Disease with Hb Chicago and Deletional Alpha Thalassemia.

Novel Mechanism of β0 Thalassemia: Missense Mutation of the Last Nucleotide of β Globin Exon 1 (G->C) Leads to Undetectable Transcript and Mutant Peptide.

Mu Opioid Receptor (OPRM-1) Polymorphisms among Patients with Sickle Cell Disease.

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American Society of Hematology

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American Society of Hematology

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