Filters
Term Search
You can select from the dropdown list OR enter your own terms to refine the search.
Last Updated: 10/31/2025
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 70 publications
Methaemoglobinemia in paediatrics: a complex diagnostic journey.
Journal: BMJ case reports
Published: February 14, 2025
Inflammatory phenotype, clinicopathologic variables, and effects of long-term methylene blue in dogs with hereditary methemoglobinemia caused by cytochrome b5 reductase deficiency.
Journal: American journal of veterinary research
Published: January 13, 2023
Oral Methylene Blue Treatment in A Dog with Cytochrome B5 Reductase Deficiency And 78, XX Testicular Disorder of Sex Development.
Journal: Topics in companion animal medicine
Published: June 08, 2021
Clinical, metabolic, and molecular genetic characterization of hereditary methemoglobinemia caused by cytochrome b5 reductase deficiency in 30 dogs.
Journal: Scientific reports
Published: August 25, 2020
An Updated View on the Molecular Pathomechanisms of Human Dihydrolipoamide Dehydrogenase Deficiency in Light of Novel Crystallographic Evidence.
Journal: Neurochemical research
Published: December 02, 2018
Congenital methaemoglobinaemia in a 61-year-old patient with normal haemoglobin levels.
Journal: The Netherlands journal of medicine
Published: May 31, 2018
Novel mutation (R192C) in CYB5R3 gene causing NADH-cytochrome b5 reductase deficiency in eight Indian patients associated with autosomal recessive congenital methemoglobinemia type-I.
Journal: Hematology (Amsterdam, Netherlands)
Published: February 28, 2018
Familial Congenital Methemoglobinemia in Pomeranian Dogs Caused by a Missense Variant in the NADH-Cytochrome B5 Reductase Gene.
Journal: Journal of veterinary internal medicine
Published: June 26, 2017
Long-term Treatment with Methylene Blue in a Dog with Hereditary Methemoglobinemia Caused by Cytochrome b5 Reductase Deficiency.
Journal: Journal of veterinary internal medicine
Published: April 30, 2017
Enzymopenic Congenital Methemoglobinemia in Children of the Republic of Sakha (Yakutia).
Journal: Journal of pediatric hematology/oncology
Published: November 24, 2016
A microplate reader-based method to quantify NADH-cytochrome b5 reductase activity for diagnosis of recessive congenital methaemoglobinemia.
Journal: Hematology (Amsterdam, Netherlands)
Published: November 20, 2016
Congenital Methemoglobinemia Type II-Clinical Improvement with Short-Term Methylene Blue Treatment.
Journal: Pediatric blood & cancer
Published: May 13, 2015
Last Updated: 10/31/2025