Cerebellar atrophy in a child with hereditary methemoglobinemia type II-Reference-Cited by-同舟云学术

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Cerebellar atrophy in a child with hereditary methemoglobinemia type II

Published:2011-04 Issue:4 Volume:33 Page:357-360
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Fusco Carlo,Soncini Giuliana,Frattini Daniele,Giustina Elvio Della,Vercellati Cristina,Fermo Elisa,Bianchi Paola

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference15 articles.

1. A novel mutation in the DIA1 gene in a patient with methemoglobinemia type II;Yilmaz;Am J Med Genet A,2005

2. Distribution of the integral membrane protein NADH-cytochrome b5 reductase in rat liver cells, studied with a quantitative radioimmunoblotting assay;Borgese;Biochem J,1986

3. Recessive hereditary methaemoglobinaemia, type II: delineation of the clinical spectrum;Ewenczyk;Brain,2008

4. Recessive hereditary methemoglobinemia: two novel mutations in the NADH-cytochrome b5 reductase gene;Fermo;Blood Cells Mol Dis,2008

5. A case of methemoglobinemia type II due to NADH-cytochrome b5 reductase deficiency: termination of the molecular basis;Aalfs;Hum Mutat,2000

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Familial Psychomotor Delay of an Uncommon Cause: Type II Congenital Methemoglobinemia;Clinical Medicine Insights: Pediatrics;2024-01

2. Neurological and Neuroimaging Features of CYB5R3-Related Recessive Hereditary Methemoglobinemia Type II;Brain Sciences;2022-01-29

3. Recessive congenital methemoglobinemia type II: Hypoplastic basal ganglia in two siblings with a novel mutation of the cytochrome b5 reductase gene;The Neuroradiology Journal;2019-01-07

4. In Vitro and In Vivo Analysis of the Effects of 3,5-DMA and Its Metabolites in Neural Oxidative Stress and Neurodevelopmental Toxicity;Toxicological Sciences;2018-12-24

5. Congenital methemoglobinemia type II in a 5-year-old boy;Clinical Case Reports;2017-12-07

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