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Alpers Syndrome (disorder)

Known as: Alpers' Disease, Neuronal Degeneration Of Childhood With Liver Disease, Progressive, Alpers Huttenlocher Disease 
A rare genetic syndrome with an autosomal recessive pattern of inheritance. It is caused by a mutation in the gene for the mitochondrial DNA… 
National Institutes of Health

Papers overview

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Highly Cited
2015
Highly Cited
2015
IMPORTANCE The prognostic role of high blood pressure and the aggressiveness of blood pressure lowering in dementia are not well… 
Highly Cited
2011
Highly Cited
2011
ESA’s upcoming satellite Sentinel-2 will provide Earth images of high spatial, spectral and temporal resolution and aims to… 
Review
2007
Review
2007
This review focuses on the role and distribution in the environment of alkane hydroxylases and their (potential) applications in… 
Highly Cited
2007
Highly Cited
2007
Twinkle is a mitochondrial replicative helicase, the mutations of which have been associated with autosomal dominant progressive… 
Highly Cited
2005
Highly Cited
2005
Mitochondrial DNA (mtDNA) polymerase gamma (Polg) is a heterodimeric enzyme containing a Pol I-like catalytic core (PolgA) and an… 
Highly Cited
2004
Highly Cited
2004
Alpers' syndrome is a fatal neurogenetic disorder first described more than 70 years ago. It is an autosomal recessive… 
Review
2002
Review
2002
Highly Cited
1993
Highly Cited
1993
We evaluated a novel system designed for rapid, point-of-care measurement of sodium, potassium, chloride, urea nitrogen, glucose…