Enzymopenic Congenital Methemoglobinemia in Children of the Republic of Sakha (Yakutia)-Reference-Cited by-同舟云学术

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Enzymopenic Congenital Methemoglobinemia in Children of the Republic of Sakha (Yakutia)

Published:2017-01 Issue:1 Volume:39 Page:42-45
ISSN:1077-4114
Container-title:Journal of Pediatric Hematology/Oncology
language:en
Short-container-title:

Author:

Burtseva Tatiana E.,Ammosova Tatiana N.,Protopopova Natalia N.,Yakovleva Svetlana Y.,Slobodchikova Maya P.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Reference12 articles.

1. Seven new mutations in the nicotinamide adenine dinucleotide reduced_cytochrome b(5) reductase gene leading to methemoglobinemia type I;Dekker;Blood,2001

2. Assignment of the DIA1 locus to chromosome 22;Fisher;Am Hum Genet,1977

3. Assignment of NADH-cytochrome b5 reductase (DlAl locus) to human chromosome 22;Junlen;Hum Genet,1978

4. The organization and the complete nucleotide sequence of the human nadh-cytochrome b5 reductase gene;Tomatsu;Gene,1989

5. An erythroid-specific transcript generates the soluble form of NADH-cytochrome b5 reductase in humans;Bulbartlli;Blood,1998

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1. Management of Congenital Methemoglobinemia in the Perioperative Setting: A Case Report and Review of Current Literature;Journal of Blood Medicine;2024-08

2. Novel Compound Heterogeneous Mutations in <i>CYB5R3</i> Gene Leading to Methemoglobinemia (Type I) in a Chinese Boy: Case Report and Relevant Comprehensive Analysis;Acta Haematologica;2024-05-24

3. Inflammatory phenotype, clinicopathologic variables, and effects of long-term methylene blue in dogs with hereditary methemoglobinemia caused by cytochrome b5 reductase deficiency;American Journal of Veterinary Research;2023-01-19

4. CYB5R3 homozygous pathogenic variant as a rare cause of cyanosis in the newborn;Clinical Biochemistry;2022-04

5. A case of congenital methaemoglobinaemia with secondary polycythemia;Journal of the Pakistan Medical Association;2022-01-29

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