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Journal Articles

Familial Polycythemia Likely Due to Novel Hemoglobin Variant Hemoglobin Hyden

Sandhya Kolagatla, Nagabhishek Moka, MD, Samuel D. Bailey, MD

Blood (2018) 132 (Supplement 1): 4925.

https://doi.org/10.1182/blood-2018-99-119590

Published: 2018

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

First-in-Man Emergency Use of Plasminogen Replacement for Respiratory Failure Due to Congenital Hypoplasminogenemia

Wolf A Hassenpflug, MD, John Moran, MD, Johanna Schrum, MD, Sarah Müller-Stöver, MD, Sonja Schneppenheim, MD, Reinhard Schneppenheim

Blood (2016) 128 (22): 3792.

https://doi.org/10.1182/blood.V128.22.3792.3792

Published: 2016

Journal Articles

Inhibition of Factor XIIa-Mediated Factor XI Activation Reduces Infarct Size in a Mouse Model of Myocardial Ischemia and Reperfusion

Christina U Lorentz, PhD, Norah G Verbout, PhD, Zhiping Cao, Helen Liu, Owen J.T. McCarty, PhD, Erik I. Tucker, PhD, Andras Gruber, MD, Donna Van Winkle, PhD

Blood (2014) 124 (21): 2873.

https://doi.org/10.1182/blood.V124.21.2873.2873

Published: 2014

Journal Articles

Methemoglobinemia In Rhesus Monkeys Due To M-Hemoglobinopathy

Osheiza Abdulmalik, DVM, MS, Larry Handt, DVM, MS, Martin Safo, PhD, Mary M Patterson, MS, DVM, Ping Wang, Caitlin A Fitzgerald, BS, Urs Giger, PD Dr. med. vet. MS FVH

Blood (2013) 122 (21): 4696.

https://doi.org/10.1182/blood.V122.21.4696.4696

Published: 2013

Journal Articles

Hereditary Haemorrhagic Telangiectasia Spectrum of ALK1/ENG Mutation

Giorgio Corinaldesi, MD, PhD

Blood (2010) 116 (21): 5066.

https://doi.org/10.1182/blood.V116.21.5066.5066

Published: 2010

Journal Articles

Anaphylactic Reaction After Replacement Therapy In Haemophilia B Patient with Inhibitor to Factor IX

Rosanna Scaraggi, Graduate, Student, Paola Giordano, Associate, Professor, Cosimo Pietro Ettorre, Medical, Doctor, Giuseppe Malcangi, Medical, Doctor, Renato Marino, Medical, Doctor, Giuseppe Lassandro, Graduate, Student, Domenico De Mattia, Professor, Francesco Antonio Scaraggi, Medical, Doctor

Blood (2010) 116 (21): 4662.

https://doi.org/10.1182/blood.V116.21.4662.4662

Published: 2010

Journal Articles

Hematopoietic Progenitor Cells From Patients with Chronic Mountain Sickness Lack the JAK2 V617F Mutation, Show Hypersensitivity to Erythropoietin and Are Inhibited by Statins.

Ricardo Amaru, MD, Martin Villarroel, MD, Hortencia Miguez, BSc, Rosario Peñaloza, BSc, Gina Torres, BSc, Tiziano Barbui, MD, Josee Golay, PhD, Alessandro Rambaldi, MD

Blood (2009) 114 (22): 1894.

https://doi.org/10.1182/blood.V114.22.1894.1894

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

Benzocaine Induced Methemoglobinemia a Potentially Life Threatening Complication after Transesophageal Echocardiogram

Shylendra B Sreenivasappa, MD, Barbara Yim, Pharm.D, R. Catchatourian, MD

Blood (2008) 112 (11): 4825.

https://doi.org/10.1182/blood.V112.11.4825.4825

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

Complement Activation in Transfusion Related Acute Lung Injury (TRALI).

Daniel R. Ambruso, MD, Christopher C. Silliman, MD, PhD, Marguerite Kelher, Gail Thurman, Patsy Giclas, PhD

Blood (2006) 108 (11): 954.

https://doi.org/10.1182/blood.V108.11.954.954

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

Is It Time To Reconfigure Lupus Anticoagulant Panels?.

Zella Rose Zeigler, MD, Andrea L. Cortese Hassett, PhD

Blood (2005) 106 (11): 2648.

https://doi.org/10.1182/blood.V106.11.2648.2648

Published: 2005

Journal Articles

Neonatal Cyanosis Due to a Novel Fetal M-Hemoglobin: Hemoglobin F-M Circleville (Gγ63 His→Leu).

Ferdane Kutlar, MD, Richard Shell, MD, Joan Atkin, MD, Dedrey Elam, Leslie Holley, Deborah Davis, Jeanette Harbin, Abdullah Kutlar, MD

Blood (2005) 106 (11): 3806.

https://doi.org/10.1182/blood.V106.11.3806.3806

Published: 2005

Journal Articles

Complement Activation Associated with Transfusion Related Acute Lung Injury (TRALI).

Daniel R. Ambruso, MD, Patsy Giclas, PhD, Christopher C. Silliman, MD, PhD, Marguerite Kelher, MS, Steve Geier, PhD

Blood (2004) 104 (11): 2721.

https://doi.org/10.1182/blood.V104.11.2721.2721

Published: 2004

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

Seven new mutations in the nicotinamide adenine dinucleotide reduced–cytochrome b 5 reductase gene leading to methemoglobinemia type I

Jan Dekker, Michel H. M. Eppink, Rob van Zwieten, Thea de Rijk, Angel F. Remacha, Lap Kay Law, Albert M. Li, Kam Lau Cheung, Willem J. H. van Berkel, Dirk Roos

Blood (2001) 97 (4): 1106–1114.

https://doi.org/10.1182/blood.V97.4.1106

Published: 2001

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Familial Polycythemia Likely Due to Novel Hemoglobin Variant Hemoglobin Hyden

Congenital Methemoglobinemia Under Diagnosed Condition with Variiable Therapeurtic Options

First-in-Man Emergency Use of Plasminogen Replacement for Respiratory Failure Due to Congenital Hypoplasminogenemia

Inhibition of Factor XIIa-Mediated Factor XI Activation Reduces Infarct Size in a Mouse Model of Myocardial Ischemia and Reperfusion

Methemoglobinemia In Rhesus Monkeys Due To M-Hemoglobinopathy

Hereditary Haemorrhagic Telangiectasia Spectrum of ALK1/ENG Mutation

Anaphylactic Reaction After Replacement Therapy In Haemophilia B Patient with Inhibitor to Factor IX

Hematopoietic Progenitor Cells From Patients with Chronic Mountain Sickness Lack the JAK2 V617F Mutation, Show Hypersensitivity to Erythropoietin and Are Inhibited by Statins.

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.

Benzocaine Induced Methemoglobinemia a Potentially Life Threatening Complication after Transesophageal Echocardiogram

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.

Complement Activation in Transfusion Related Acute Lung Injury (TRALI).

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

Is It Time To Reconfigure Lupus Anticoagulant Panels?.

Neonatal Cyanosis Due to a Novel Fetal M-Hemoglobin: Hemoglobin F-M Circleville (Gγ63 His→Leu).

Complement Activation Associated with Transfusion Related Acute Lung Injury (TRALI).

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

Seven new mutations in the nicotinamide adenine dinucleotide reduced–cytochrome b 5 reductase gene leading to methemoglobinemia type I

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