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2004, ISBN 9781402028977, xvii, 288
"Neuroacanthocytosis Syndromes" is the first comprehensive review of a field that has not yet received the attention it deserves. Affecting the brain as well... 
Brain | Clinical & internal medicine | Molecular aspects | Erythrocytes | Diseases | Human Genetics | Neurosciences | Biomedicine
Book
2002, 3rd ed., Oxford monographs on medical genetics, ISBN 0198510608, Volume 45, xvi, 558
Book
2011, Frontiers in neuroscience, ISBN 0849390001, xx, 312
In 1993, the genetic mutation responsible for Huntington’s disease (HD) was identified. Considered a milestone in human genomics, this discovery has led to... 
Huntington Disease | physiopathology | drug therapy | Molelcular aspects | Pathophysiology | methods | Neuropharmacology | Huntington's disease | Drug Discovery | Biotechnology | Neuroscience
Book
1981, ISBN 0387105883, xvii, 192
Book
1989, Johns Hopkins series in contemporary medicine and public health., ISBN 0801838606, x, 251
Book
1993, ISBN 0521459834, Volume 23., 46
This report presents the findings of a study of people affected by Huntington's chorea and their unaffected relatives, and in particular, of the incidence of... 
Book
04/2018, ISBN 9781536138542
Book
10/2017, Handbook of clinical neurology, ISBN 9780128018934, Volume 144, 289
'Huntington Disease' summarizes the most recent findings related to the disease, providing both cutting edge coverage for clinical/research specialists looking... 
Huntington's disease
eBook
Journal of Child Neurology, ISSN 0883-0738, 01/2011, Volume 26, Issue 3, pp. 369 - 372
Acute secondary neurological deterioration after herpes simplex encephalitis has been reported. An immune-mediated process is thought to be responsible for... 
Chorea
Journal Article
Clinical Genetics, ISSN 0009-9163, 10/2014, Volume 86, Issue 4, pp. 373 - 377
The aim of this study was to identify the relative frequency of Huntington's disease (HD) and HD‐like (HDL) disorders HDL1, HDL2, spinocerebellar ataxia type 2... 
HDL1 | neuroferritinopathy | chorea‐acanthocytosis | DRPLA | HDL2 | spinocerebellar ataxia type 2 | HD‐like | Huntington disease | SCA2 | Brazil | benign hereditary chorea | Huntington disease‐like 2 | Huntington disease-like 2 | Spinocerebellar ataxia type 2 | Benign hereditary chorea | Chorea-acanthocytosis | Neuroferritinopathy | HD-like | DIAGNOSIS | PHENOTYPE | GENE | CHOREA | EXPANSION | GENETICS & HEREDITY | HUNTINGTON-DISEASE-LIKE-2 | chorea-acanthocytosis | TRINUCLEOTIDE REPEAT | Heredodegenerative Disorders, Nervous System - genetics | Heredodegenerative Disorders, Nervous System - pathology | Humans | Huntington Disease - pathology | Middle Aged | Dementia - diagnosis | Male | Dementia - epidemiology | Dementia - genetics | Spinocerebellar Ataxias - diagnosis | Adult | Female | Huntington Disease - diagnosis | Chorea - diagnosis | Spinocerebellar Ataxias - genetics | Dementia - pathology | Cognition Disorders - pathology | Spinocerebellar Ataxias - epidemiology | Heredodegenerative Disorders, Nervous System - diagnosis | Cognition Disorders - genetics | Spinocerebellar Ataxias - pathology | Chorea - pathology | Cognition Disorders - diagnosis | Huntington Disease - epidemiology | Phenotype | Chorea - epidemiology | Heredodegenerative Disorders, Nervous System - epidemiology | Huntington Disease - genetics | Trinucleotide Repeat Expansion - genetics | Chorea - genetics | Cognition Disorders - epidemiology | Huntington's chorea | Epidemiology | Neurological disorders | Genetic disorders
Journal Article
2008, ISBN 9783540716921, 315
This book contains the latest research regarding the neurodegenerative conditions known as neuroacanthocytosis. Recent advances have identified the range of... 
Brain | Clinical & internal medicine | Human genetics | Human Genetics | Neurology | Neurosciences | Biomedicine
eBook
BBA - Bioenergetics, ISSN 0005-2728, 08/2016, Volume 1857, pp. e103 - e104
Journal Article
Journal Article
Parkinsonism and Related Disorders, ISSN 1353-8020, 06/2012, Volume 18, Issue 5, pp. 458 - 461
Journal Article
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