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ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA

Known as: Early-onset ataxia with oculomotor apraxia and hypoalbuminemia, Early-Onset Ataxia with Ocular Motor Apraxia and Hypoalbuminemia, Ataxia-oculomotor apraxia syndrome 
National Institutes of Health

Related topics

Related topics

16 relations

Broader (3)

ApraxiasCerebellar AtaxiaHypoalbuminemia
Ataxia, TruncalAutosomal recessive inheritanceCerebellar atrophyChronic progressive external ophthalmoplegia
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Papers overview

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Highly Cited
2013
Highly Cited
2013
Phase III trial of chemoradiotherapy for anaplastic oligodendroglioma: long-term results of RTOG 9402.
PURPOSE Anaplastic oligodendrogliomas, pure (AO) and mixed (anaplastic oligoastrocytoma [AOA]), are chemosensitive, especially if… Expand
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Review
2012
Review
2012
Archaeal and bacterial ammonia-oxidisers in soil: the quest for niche specialisation and differentiation.
Autotrophic archaeal and bacterial ammonia-oxidisers (AOA and AOB) drive soil nitrification. Ammonia limitation, mixotrophy, and… Expand
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Review
2012
Review
2012
Trace Metal Requirements for Microbial Enzymes Involved in the Production and Consumption of Methane and Nitrous Oxide
Fluxes of greenhouse gases to the atmosphere are heavily influenced by microbiological activity. Microbial enzymes involved in… Expand
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Highly Cited
2011
Highly Cited
2011
Induction of CD8+ T-cell responses against novel glioma-associated antigen peptides and clinical activity by vaccinations with {alpha}-type 1 polarized dendritic cells and polyinosinic-polycytidylic…
PURPOSE A phase I/II trial was performed to evaluate the safety and immunogenicity of a novel vaccination with α-type 1 polarized… Expand
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Highly Cited
2006
Highly Cited
2006
The Impact of Proficiency on Syntactic Second-language Processing of German and Italian: Evidence from Event-related Potentials
The present study investigated the role of proficiency in late second-language (L2) processing using comparable stimuli in German… Expand
Review
2006
Review
2006
Autosomal recessive cerebellar ataxias
Autosomal recessive cerebellar ataxias (ARCA) are a heterogeneous group of rare neurological disorders involving both central and… Expand
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Highly Cited
2003
Highly Cited
2003
Timed picture naming in seven languages
Timed picture naming was compared in seven languages that vary along dimensions known to affect lexical access. Analyses over… Expand
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Highly Cited
2002
Highly Cited
2002
Age of Acquisition Effects in Word Reading and Other Tasks
Recent studies have suggested that age of acquisition (AoA) has an impact on skilled reading independent of factors such as… Expand
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Highly Cited
2001
Highly Cited
2001
The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin
The newly recognized ataxia–ocular apraxia 1 (AOA1; MIM 208920) is the most frequent cause of autosomal recessive ataxia in Japan… Expand
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Highly Cited
1988
Highly Cited
1988
Genetic Groups in an Animal Model
Abstract Rules are presented for assigning coefficients to the genetic group portion(s) of the mixed model equations after… Expand
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