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Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant

Known as: Multiple Sclerosis-Like Disorder, PELIZAEUS-MERZBACHER DISEASE, AUTOSOMAL DOMINANT OR LATE-ONSET TYPE, FORMERLY, ADLD 
 
National Institutes of Health

Papers overview

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2017
2017
Isolated focal dystonia is a debilitating movement disorder of unknown pathophysiology. Early studies in focal dystonias have… Expand
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2016
2016
Aberrant sensory processing plays a fundamental role in the pathophysiology of dystonia; however, its underpinning neural… Expand
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2016
2016
People with ADLD develop signs and symptoms of the condition in adulthood, typically in their forties or fifties. The first signs… Expand
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2016
2016
Infection with Hepatitis C Virus (HCV) is one of the most important risk factor of hepatocellular carcinoma (HCC). HCV is… Expand
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2015
2015
Objective Duplication of the LMNB1 gene encoding lamin B1 causes adult‐onset autosomal‐dominant leukodystrophy (ADLD) starting… Expand
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2014
2014
To facilitate the intuitional analysis of protein sequences, a novel graphical representation of protein sequences called ADLD… Expand
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2013
2013
The nuclear lamina underlies the inner nuclear membrane and consists of a proteinaceous meshwork of intermediate filaments: the A… Expand
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2013
2013
IntroductionAdult-onset ADLD with autonomic symptoms is a rare disease with a clinical course somewhat similar to chronic… Expand
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2011
2011
Adult-onset autosomal dominant leukodystrophy (ADLD, OMIM accession number 169500) is a slowly progressive neurological disorder… Expand
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2001
2001
BACKGROUND Case reports and clinical observations suggest that fluctuating cognition (FC) is common in all the major dementias… Expand
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