Riboflavin-responsive multiple Acyl-CoA dehydrogenation deficiency in 13 cases and a literature review in mainland Chinese patients
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Title
Riboflavin-responsive multiple Acyl-CoA dehydrogenation deficiency in 13 cases and a literature review in mainland Chinese patients
Authors
Keywords
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Journal
JOURNAL OF HUMAN GENETICS
Volume 59, Issue 5, Pages 256-261
Publisher
Springer Nature
Online
2014-02-13
DOI
10.1038/jhg.2014.10
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Related references
Note: Only part of the references are listed.- Secondary coenzyme Q10 deficiency and oxidative stress in cultured fibroblasts from patients with riboflavin responsive multiple Acyl-CoA dehydrogenation deficiency
- (2013) N. Cornelius et al. HUMAN MOLECULAR GENETICS
- Increased muscle coenzyme Q10 in riboflavin responsive MADD with ETFDH gene mutations due to secondary mitochondrial proliferation
- (2013) Bing Wen et al. MOLECULAR GENETICS AND METABOLISM
- Genetic and cellular modifiers of oxidative stress: What can we learn from fatty acid oxidation defects?
- (2013) Rikke Katrine Jentoft Olsen et al. MOLECULAR GENETICS AND METABOLISM
- A Case of Late-onset Riboflavin Responsive Multiple acyl-CoA Dehydrogenase Deficiency with Novel Mutations in ETFDH Gene
- (2012) Zhang-Ning Zhao et al. CNS Neuroscience & Therapeutics
- A Case of Late Onset Riboflavin-responsive Multiple Acyl-CoA Dehydrogenase Deficiency Manifesting as Recurrent Rhabdomyolysis and Acute Renal Failure
- (2011) Rumiko Izumi et al. INTERNAL MEDICINE
- Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>A
- (2011) Zhi-Qiang Wang et al. JOURNAL OF MOLECULAR MEDICINE-JMM
- Multiple Acyl-CoA-dehydrogenase deficiency (MADD) — A novel mutation of electron-transferring-flavoprotein dehydrogenase ETFDH
- (2011) A.B. Lämmer et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- The effects of glucocorticoids on adipose tissue lipid metabolism
- (2011) Ashley J. Peckett et al. METABOLISM-CLINICAL AND EXPERIMENTAL
- Subacute myopathy in a mature patient due to multiple acyl-coenzyme a dehydrogenase deficiency
- (2011) Pierre Kaminsky et al. MUSCLE & NERVE
- Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency with unknown genetic defect
- (2011) Maria Sofia Cotelli et al. NEUROLOGICAL SCIENCES
- High resolution melting analysis facilitates mutation screening of ETFDH gene: Applications in riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency
- (2010) Tze-Kiong Er et al. CLINICA CHIMICA ACTA
- High frequency of ETFDH c.250G>A mutation in Taiwanese patients with late-onset lipid storage myopathy
- (2010) M-Y Lan et al. CLINICAL GENETICS
- Glutaric Aciduria Type 2, Late Onset Type in Thai Siblings With Myopathy
- (2010) Pornswan Wasant et al. PEDIATRIC NEUROLOGY
- Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency
- (2009) Lap-Kay Law et al. CLINICA CHIMICA ACTA
- Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations
- (2009) B. Wen et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Clinical and genetic analysis of lipid storage myopathies
- (2009) Aya Ohkuma et al. MUSCLE & NERVE
- Role of Flavinylation in a Mild Variant of Multiple Acyl-CoA Dehydrogenation Deficiency
- (2008) Bárbara J. Henriques et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Clinical and molecular investigations of Japanese cases of glutaric acidemia type 2
- (2008) Yuka Yotsumoto et al. MOLECULAR GENETICS AND METABOLISM
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