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Journal Articles

Congenital Methemoglobinemia Under Diagnosed Condition with Variiable Therapeurtic Options

Mohamed A. Yassin, MBBS,MSc,CABM,FACP,MSC, Dina Sameh Soliman, PhD

Blood (2017) 130 (Supplement 1): 4746.

https://doi.org/10.1182/blood.V130.Suppl_1.4746.4746

Published: 2017

Journal Articles

Cytochrome B5 Reductase T116S Polymorphism Is Associated with Decreased Risk of Severe Anemia Among Zambian Children with Malaria

Victor R. Gordeuk, MD, Mehdi Nouraie, PhD, Xiaomei Niu, PhD, Jessica Nachel DelBove, Josef T. Prchal, MD

Blood (2010) 116 (21): 4233.

https://doi.org/10.1182/blood.V116.21.4233.4233

Published: 2010

Journal Articles

Cytochrome b5 Reductase T116S Mutation and Hemolysis in Sickle Cell Disease.

Mehdi Nouraie, Noel S. Reading, PhD, Andrew Campbell, Caterina Minniti, M.D., Sohail R Rana, MD, Lori Luchtman-Jones, MD, Craig Sable, Niti Dham, MD, Gregory Ensing, Gregory J Kato, Mark Gladwin, MD, Oswaldo L Castro, MD, Josef T. Prchal, MD, Victor R. Gordeuk, MD

Blood (2009) 114 (22): 903.

https://doi.org/10.1182/blood.V114.22.903.903

Published: 2009

Journal Articles

Type I Methemoglobinemia Caused by the Cytochrome b5 Reductase 806C>T Mutation Is Present in the Indigenous Evenk People of Yakutia.

Tatyana Burtseva, Tatiana Ammosova, PhD, Josef T. Prchal, MD, Vyacheslav Chasnyk, MD, Sergei Nekhai, PhD, Victor R. Gordeuk, MD

Blood (2009) 114 (22): 2588.

https://doi.org/10.1182/blood.V114.22.2588.2588

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

Identification of Two Novel Mutations in the CYB5R3 Gene in Five Cases of Type I Methemoglobinemia

Felipe R. Lorenzo, V, MD, PhD, Roberto H Nussenzveig, PhD, John D Phillips, PhD, Stanley L. Schrier, MD, Josef T. Prchal, MD

Blood (2008) 112 (11): 3854.

https://doi.org/10.1182/blood.V112.11.3854.3854

Published: 2008

Journal Articles

Recessive Congenital Methaemoglobinaemia: Three New Mutations in the NADH-Cytochrome b5 Reductase Gene.

Elisa Fermo, PhD, Paola Bianchi, PhD, Cristina Vercellati, PhD, Anna P. Marcello, PhD, Wilma Barcellini, MD, Ornella Marangoni, MD, Massimo Garatti, MD, Alberto Zanella, MD

Blood (2006) 108 (11): 1576.

https://doi.org/10.1182/blood.V108.11.1576.1576

Published: 2006

Journal Articles

A Novel Heterologous Expression System for Characterization of Individual NADH-Cytochrome b 5 Reductase Variants in Recessive Congenital Methemoglobinemia.

Melanie J. Percy, PhD, L. J. Crowley, PhD, C. A. Davis, PhD, J. Boudreaux, MD, D. M. Layton, MD, M. F. McMullin, MD, T. R. Lappin, PhD, M. J. Barber, DPhil

Blood (2005) 106 (11): 1676.

https://doi.org/10.1182/blood.V106.11.1676.1676

Published: 2005

Journal Articles

The First Indian Mutation of NADH-Cytochrome b5 Reductase as a Cause for Type 1 Methemoglobinemia.

Hima B. Lingam, MD, Roberto H. Nussenveig, PhD, Qiqing Zhu, PhD, Naijie Jing, PhD, Josef T. Prchal, MD

Blood (2005) 106 (11): 1677.

https://doi.org/10.1182/blood.V106.11.1677.1677

Published: 2005

Journal Articles

Heterogeneity of Molecular Biology of Methemoglobinemia; Study of Eight Consecutive Patients.

Jey Maran, M.D., Yongli Guan, Ching-Nan Ou, Ph.D, Josef T. Prchal, M.D.

Blood (2004) 104 (11): 1587.

https://doi.org/10.1182/blood.V104.11.1587.1587

Published: 2004

Journal Articles

Introduction: congenital methemoglobinemia revisited

Quentin Gibson

Blood (2002) 100 (10): 3445–3446.

https://doi.org/10.1182/blood-2002-08-2601

Published: 2002

Journal Articles

Familial idiopathic methemoglobinemia revisited: original cases reveal 2 novel mutations in NADH-cytochrome b5 reductase

Melanie J. Percy, Matthew J. S. Gillespie, Geraldine Savage, Anne E. Hughes, Mary Frances McMullin, Terry R. J. Lappin

Blood (2002) 100 (10): 3447–3449.

https://doi.org/10.1182/blood-2002-05-1405

Published: 2002

Journal Articles

A novel mutation in the NADH-cytochrome b5 reductase gene of a Chinese patient with recessive congenital methemoglobinemia

Yao Wang, Yu-Shui Wu, Pei-Zhen Zheng, Wen-Xi Yang, Guo-An Fang, Yu-Chai Tang, Fei Xie, Feng-Hua Lan, Zhong-Yong Zhu

Blood (2000) 95 (10): 3250–3255.

https://doi.org/10.1182/blood.V95.10.3250

Published: 2000

Journal Articles

Serine-proline replacement at residue 127 of NADH-cytochrome b5 reductase causes hereditary methemoglobinemia, generalized type

Y Kobayashi, Y Fukumaki, T Yubisui, J Inoue, Y Sakaki

Blood (1990) 75 (7): 1408–1413.

https://doi.org/10.1182/blood.V75.7.1408.1408

Published: 1990

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Congenital Methemoglobinemia Under Diagnosed Condition with Variiable Therapeurtic Options

Cytochrome B5 Reductase T116S Polymorphism Is Associated with Decreased Risk of Severe Anemia Among Zambian Children with Malaria

Cytochrome b5 Reductase T116S Mutation and Hemolysis in Sickle Cell Disease.

Type I Methemoglobinemia Caused by the Cytochrome b5 Reductase 806C>T Mutation Is Present in the Indigenous Evenk People of Yakutia.

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

Identification of Two Novel Mutations in the CYB5R3 Gene in Five Cases of Type I Methemoglobinemia

Recessive Congenital Methaemoglobinaemia: Three New Mutations in the NADH-Cytochrome b5 Reductase Gene.

A Novel Heterologous Expression System for Characterization of Individual NADH-Cytochrome b 5 Reductase Variants in Recessive Congenital Methemoglobinemia.

The First Indian Mutation of NADH-Cytochrome b5 Reductase as a Cause for Type 1 Methemoglobinemia.

Heterogeneity of Molecular Biology of Methemoglobinemia; Study of Eight Consecutive Patients.

Introduction: congenital methemoglobinemia revisited

Familial idiopathic methemoglobinemia revisited: original cases reveal 2 novel mutations in NADH-cytochrome b5 reductase

A novel mutation in the NADH-cytochrome b5 reductase gene of a Chinese patient with recessive congenital methemoglobinemia

Serine-proline replacement at residue 127 of NADH-cytochrome b5 reductase causes hereditary methemoglobinemia, generalized type

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