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Methemoglobinemia
Hemoglobinopathies: Clinical & Hematologic Features And
The Role of Methemoglobin and Carboxyhemoglobin in COVID-19: a Review
Congenital Methemoglobinemia-Induced Cyanosis in Assault Victim
Methemoglobinemia in Patient with G6PD Deficiency and SARS-Cov-2
Methemoglobinemia and Ascorbate Deficiency in Hemoglobin E Β Thalassemia: Metabolic and Clinical Implications
A Rare Case of Congenital Methemoglobinemia With
The Formation of Methemoglobin and Sulfhemoglobin During Sulfanilamide Therapy
Methemoglobinemia: Cyanosis and Street Methamphetamines
Congenital Methemoglobinemia Identified by Pulse Oximetry Screening Jennifer Ward, Jayashree Motwani, Nikki Baker, Matthew Nash, Andrew K
Inborn Defects in the Antioxidant Systems of Human Red Blood Cells
Nitrate and Methemoglobinemia Drinking Water with High Nitrate Can Cause a Potentially Fatal Disorder Called Methemoglobinemia
Demystifying Methemoglobinemia
Blueprint Genetics Anemia Panel
An Unusual Case of Methemoglobinemia
Significant Methemoglobinemia with Bovine Hemoglobin Infusion in A
Carbohydrate Metabolism Synopsis of Glycolytic Enzyme Deficiencies
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY Date of Publication: October 14, 2020
HBB Gene Hemoglobin Subunit Beta
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Clinical, Metabolic, and Genetic Characterization of Hereditary Methemoglobinemia Caused by Cytochrome B5 Reductase Deficiency in Cats
The Effect of Methemoglobin Formation in Sickle Cell Disease
Congenital Methemoglobinemia and Unstable Hemoglobin Variant in a Child with Cyanosis
Oral L-Glutamine Powder for the Treatment of Sickle Cell Disease
Severe Methemoglobinemia and Hemolytic Anemia from Aniline
Enzyme Assays in Diseases of Erythrocytes
Congenital Methemoglobinemia. a Clinical and Biochemical Study of a Case
Hereditary Nonspherocytic Hemolytic Disease Associated with an Altered Phospholipid Composition of the Erythrocytes
Risk of Methemoglobinemia in the Medicine Cabinet
With the Methemoglobin Levels in Recessive Congenital
Lidocaine-Induced Methemoglobinemia: a Clinical Reminder Mark Barash, DO Keith A
Glucose-6-Phosphate Dehydrogenase Deficiency- Associated Hemolytic Anemia and Methemoglobinemia in a Patient Treated with Hydroxychloroquine in the Era of COVID-19
Methemoglobinemia ______
Acute Cyanosis Developing After the Placement of Central Venous Catheter: Methemoglobinemia Related to Local Prilocaine
Comprehensive Hemoglobin Analysis HBA1/2 ( Α-Globin) And
Inhaled Nitric Oxide Improves Survival Rates During Hypoxia in a Sickle Cell
Hereditary Hemolytic Anemia Panel, Sequencing
Acute Methemoglobinemia with Hemolytic Anemia Following Bio-Organic Plant Nutrient Compound Exposure: Two Case Reports
How Safe Is Prilocaine As a Local Anesthetic in Children Younger Than 2 Years of Age: a Case Series
Morbidity and Mortality Weekly Report
Life-Threatening Methemoglobinemia
Methemoglobinemia and Sulfhemoglobinemia in Two Pediatric Patients After Ingestion of Hydroxylamine Sulfate
Glucose-6-Phosphate Dehydrogenase Deficiency
Hemoglobin Variants – Pathomechanism, Symptoms and Diagnosis
Causes and Clinical Significance of Increased Methemoglobin
Risk of Serious and Potentially Fatal Blood Disorder Prompts FDA Action
A Case of Sulfhemoglobinemia in a Child with Chronic Constipation
Acquired Hemoglobin Disorders
Drugs May Be Induced Methemoglobinemia
NITRATES, METHEMOGLOBINEMIA, and DRINKING WATER: a Factsheet for Clinicians
Congenital Methemoglobinemia: a Rare Cause of Cyanosis in the Newborn—A Case Report
Pseudo-Methemoglobinemia Induced by Phenazopyridine, a Diagnostic Challenge
Delayed Diagnosis in Army Ranger Postdeployment Primaquine-Induced Methemoglobinemia
Polycythemia Vera (PV)
Case Reports
A Case Presentation of Neonatal Methemoglobinemia
A 3 Year Old with Hypoxia Other Treatments Besides Oxygen
Congenital Methemoglobinemia Misdiagnosed As Polycythemia Vera