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Research and complicity: the case of Julius Hallervorden

FG Miller - Journal of Medical Ethics, 2011 - jme.bmj.com
The charge of complicity has been raised in debates over the ethics of fetal tissue transplantation
and embryonic stem cell research. However, the applicability of the concept of complicity to these
types of research is neither clear nor uncontroversial. This article discusses the historical ...
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Young-Onset Parkinsonism in a Hong Kong Chinese Man With Adult-Onset Hallervorden-Spatz Syndrome

CM Mak, B Sheng, HH Lee, K Lau… - International …, 2011 - informahealthcare.com
Neurodegeneration with brain iron accumulation (NBIA) is a heterogeneous group of disorders
varied in genetic etiologies, clinical presentations, and radiological features. NBIA is an iron
homeostasis disorder with progressive iron accumulation in the central nervous systems ...
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Hallervorden-Spatz syndrome: a rare cause of extrapyramidal manifestations

[HTML] from annalsofneurosciences.orgKV Vinod… - Annals of Neurosciences, 2011 - annalsofneurosciences.org
Hallervorden-Spatz syndrome [HSS] is a rare neurodegenerative disorder of autosomal recessive
inheritance characterized by accumulation of iron in basal ganglia. The syndrome encompasses
a spectrum of clinically heterogeneous disorders characterized by common features of ...
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Adult onset Hallervorden-Spatz disease with psychotic symptoms.

P Del Valle-López, R Pérez-García… - Actas españolas de …, 2011 - ncbi.nlm.nih.gov
Hallervorden-Spatz disease is a rare neurological disorder characterized by pyramidal and extrapyramidal
manifestations, dysarthria and dementia. Its onset is usually in childhood and most patients have
a fatal outcome in few years. A high percentage of cases are hereditary with a recessive ...

Conversion disorder as initial diagnosis in pantothenate kinase associated neurodegeneration

I Vansteenkiste, WA van Gool, DJ Hofstee… - Journal of …, 2011 - Springer
... Dear Sirs, We present a patient with the atypical form of PKAN (pantothenate kinase-associated
neurodegeneration, previ- ously called the syndrome of Hallervorden and Spatz) that was caused
by a new mutation in the PANK2 gene, with a peculiar type of bradykinesia. ...
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