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Amimia

National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
[Amimia in Parkinson's disease. Significance and correlation with the clinical features].
INTRODUCTION Reduced facial expression or amimia is one of the most typical characteristics of Parkinson's disease (PD). Despite… 
2018
2018
Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia
Abstract The Neurofascins (NFASCs) are a family of proteins encoded by alternative transcripts of NFASC that cooperate in the… 
2018
2018
Amimia en la enfermedad de Parkinson. Significado y correlación con la clínica
Introduccion. La amimia o reduccion de la expresion facial es una de las caracteristicas mas tipicas de la enfermedad de… 
Review
2017
Review
2017
Prodromal stage of disease (dementia) with Lewy bodies, how to diagnose in practice?
Disease with Lewy bodies or dementia with Lewy bodies (DLB), particularly at the prodromal stage, is a complex disease to… 
2014
2014
[Brainstem dysgenesis: functional prognosis and rehabilitative treatment. A series of nine cases].
INTRODUCTION Brainstem dysgenesis is a heterogeneous clinical entity, with low incidence and high clinical variability, which… 
2011
2011
Acute psychosis in anti-NMDA-receptor encephalitis.
2004
2004
Transiente neonatale Myasthenia gravis
Zusammenfassung10–20% der Kinder von Müttern mit Myasthenia gravis entwickeln selbst eine transiente neonatale Myasthenia gravis… 
2002
2002
Transiente neonatale Myasthenia gravis
Zusammenfassung10-20% der Kinder von Müttern mit Myasthenia gravis entwickeln selbst eine transiente neonatale Myasthenia gravis… 
1988
1988
Extrapyramidal syndrome and depression induced by flunarizine.
Apathy, mood depression and extrapyramidal signs consisting of akinesia, amimia, gait apraxia, slight rigidity and tremor were… 
1986
1986
A case of ornithine transcarbamylase deficiency with Rett syndrome manifestations.
We have studied an 8-year-old girl with ornithine transcarbamylase deficiency with many of the manifestations of Rett syndrome… 
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