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Mitochondrial complex II deficiency

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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "Mitochondrial complex II deficiency" returned 0 free, full-text review articles. First 0 results:
Infertility and recurrent miscarriage with complex II deficiency-dependent mitochondrial oxidative stress in animal models.
Last Updated: Dec 30, 2016

Oxidative stress is associated with some forms of both male and female infertility. However, there is insufficient knowledge of the influence of oxidative stress on the maintenance of a viable pregnancy, including pregnancy complications and fetal development. There are a number of ...

Mitochondrial complex I deficiency of nuclear origin II. Non-structural genes.
Last Updated: Dec 10, 2019

Complex I deficiency is the most frequent cause of respiratory chain diseases. This large multiprotein complex is composed in human of 45 structural subunits, of which 7 are mitochondrial-encoded and 38 are nuclear-encoded. Most of the pathological mutations responsible for complex ...

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Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "Mitochondrial complex II deficiency" returned 0 free, full-text editorial articles. First 0 results:
No publications were found for this category.
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Mitochondrial complex II deficiency" returned 6 free, full-text research articles. First few results:
Riboflavin transporter deficiency mimicking mitochondrial myopathy caused by complex II deficiency.
Last Updated: Sep 30, 2020

Biallelic likely pathogenic variants in SLC52A2 and SLC52A3 cause riboflavin transporter deficiency. It is characterized by muscle weakness, ataxia, progressive ponto-bulbar palsy, amyotrophy, and sensorineural hearing loss. Oral riboflavin halts disease progression and may reverse ...

Heterogeneity of FHF1 related phenotype: Novel case with early onset severe attacks of apnea, partial mitochondrial respiratory chain complex II deficiency, neonatal onset seizures without neurodegeneration.
Last Updated: Mar 27, 2019

We report the case of a child prospectively followed in our institution for a severe, neonatal onset epilepsy presenting with severe attacks of apnea that were not initially recognized as seizure since they were not associated with any abnormal movement and since interictal EEG was ...

Renal Tubular Mitochondrial Abnormalities in Complex II/III Respiratory Chain Deficiency.
Last Updated: Dec 10, 2019

Defects in the respiratory chain may present with a wide spectrum of clinical signs and symptoms. In this "Images in Pathology" discussion we correlate the clinical, histologic, and ultrastructural findings in a 12-year-old male with a complex II/III respiratory chain deficiency and ...

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