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Journal Articles

Congenital Methemoglobinemia Under Diagnosed Condition with Variiable Therapeurtic Options

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Mohamed A. Yassin, MBBS,MSc,CABM,FACP,MSC, Dina Sameh Soliman, PhD
Journal: Blood
Blood (2017) 130 (Supplement 1): 4746.
https://doi.org/10.1182/blood.V130.Suppl_1.4746.4746
Published: 2017
Journal Articles

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

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Hima B. Lingam, MD, Roberto H. Nussenveig, PhD, Qiqing Zhu, PhD, Naijie Jing, PhD, Josef T. Prchal, MD
Journal: Blood
Blood (2005) 106 (11): 1677.
https://doi.org/10.1182/blood.V106.11.1677.1677
Published: 2005
Journal Articles

A Simple Spot Screening Test for Fast Detection of Red Cell NADH-Diaphorase Deficiency

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JEAN-CLAUDE KAPLAN, M.D., ANNE-MARIE NICOLAS, ALENA HANZLICKOVA-LEROUX, ERNEST BEUTLER, M.D.
Journal: Blood
Blood (1970) 36 (3): 330–333.
https://doi.org/10.1182/blood.V36.3.330.330
Published: 1970